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{"sheet":"LIST OF ITEMS","index":0,"n_rows":12,"n_cols":3,"rows_kept":12}
[null,"GT/GDH/020/2026 THE SUPPLY,DELIVERY,INSTALLATION,COMMISSIONING,AND MAINTANACE OF SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS  GAUTENG DEPARTMENT OF HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS "]
["No:","LIST OF ITEMS","BIDDER TO SELECT PREFERED CHOICE OF ITEM/S"]
[1,"MULTI SLOT CR READER"]
[2,"FIXED FLUOROSCOPY SCREENING UNIT WITH C-ARM AND FLAT PANEL DETECTOR (FPD)"]
[3,"REMOTE CONTROL TABLE FLUOROSCOPY SCREENING UNIT  WITH FLAT PANEL DETECTOR (FPD)"]
[4,"DIGITAL FLAT PANEL"]
[5,"PANELIPSE/PANOREX"]
[6,"CT SCANNER 128 SLICE"]
[7,"CT SCANNER 256 SLICE"]
[8,"MRI 1,5T"]
[9,"MRI 3T"]
[10,"ONE SHOT SCOLIOSIS IMAGING"]

{"sheet":"1. MULTI SLOT CR","index":1,"n_rows":38,"n_cols":7,"rows_kept":38,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[36,0,36,1],[37,0,37,1]]}
["                                                              ANNEXURE A: TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 32 out of 39 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item no. 1","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
[null,"Multi Slot CR Reader"]
["A","Multi Slot CR System"]
["A.1","A computerised radiography unit using storage phosphor screens/IP and a reader must be offered. It must be the latest model of a Multislot CR System with multiple IP feed . Details of system, including the material used as phosphor must stated. ",2]
["A.2","A UPS  (in series connection to main power supply) / online (uninterruptable power supply unit) suitable for the workstation,  must be included in the tender price. Technical data sheets for the UPS must be provided in supporting documents.",2]
["A.3","Online UPS 3kVA or higher",1]
["A.4","It must be possible to enter patient data manually for emergencies or when the network  is down. Details of available softwares emergency functionalities must be stated in supporting documents.",2]
["A.5","The cassette throughput per hour for 35cm x 43cm, must be 60 or more  imaging plates per hour. ",1]
["A.6","The IP Feed / Load time in seconds for 35cm x43cm imaging plate must not be more than 60 seconds. The IP Feed / Load time is stated.",1]
["A.7","The unit must have two or more IP Feed slots. A two or more cassettes stacker multislot machine must be provided.",2]
["A.8","The full image preview on the system must not be more than 60 seconds. Full image preview time-frame is stated.",2]
["A.9","The image resolution mode/pixel pitch must not be more than 100 micron. The available image resolution modes pixel pitch on the system must be stated in supporting documents.",1]
["A.10","Grayscale resolution: (a)  A minimum of 14 bits per pixel  acquisition and ( b)A  minimum of 12 bits per pixel display  must be possible. Details are stated in supporting documents.",1]
["A.11","The workstation must have a 19 inch flat-panel monitor (or bigger/better), touch screen, full colour monitor for data input, image control and system control, keyboard and a mouse must be provided.",1]
["A.12","The system must be able to perform image post-processing functionalities. ",1]
["A.13","DICOM 3.0 Compatible: print class, storage SCU, worklist management and transfer of images from CR to Laser Printer, CD/DVD, USB, Storage Hard Drive, PACS/RIS. Image viewer must be fully DICOM compatible, External storage Hard-drive fully DICOM compatible. ",2]
["A.14","The configuration between the processed images on the CR System and images to the receivers of these images,  such as PACS, Laser Printer and CD/DVD/USB, must be properly calibrated or licence activated during software upgrades of all systems in the image processing and image transfer chain.  ",1]
["A.15","The system must have a configureable auto delete function. ",1]
["A.16","The system must be able to store 2000 images on the system  before auto-deletion occurs. The system must alert the end-user of the remaining storage space before auto-deletion occurs. ",2]
["A.17","Maximum storage capacity must be stated in GB and according to maximum number  of image storage capability.",1]
["A.18","The following CR cassettes and Imaging Plates(IP) for the system must be provided (to be included in the pricing schedule):"]
["A18.1","35cm x 43cm standard resolution x   10",2]
["A18.2","35cm x 35cm standard resolution x  4",2]
["A18.3","24cm x 30cm standard resolution x  10",2]
["A18.4","18cm x 24cm standard resolution x   4",2]
["A18.5","The CR reader must have brake locking castors/wheels. ",2]
["A18.6","The system must have an audible alarm / iluminating light sensor to alert for cassette removal.",1]
["A18.7","The system must have an internal barcode reader for image plate identification to identify faulty imaging plates.",2]
["A18.8","The system must be capable of multiformat printing.",1]
["B","Optional Items:"]
["B.1","A  cabinet for the storage of imaging plates must be included in the offer as optional.",1]
["Total score",null,{"$f":"SUM(C9:C36)","v":39}]
["minimum threshold",null,32]

{"sheet":"2.FIXED FLUOROSCOPY SCREENING  ","index":2,"n_rows":79,"n_cols":7,"rows_kept":79,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[77,0,77,1],[78,0,78,1]]}
["                                                              TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 68 out of 86 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item no. 2","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet  /  Any Supporting Document"]
[null,"FIXED FLUOROSCOPY SCREENING UNIT WITH C-ARM AND FLAT PANEL DETECTOR (FPD)"]
["A","X-Ray Generator"]
["A.1","Micro-processor controlled high frequency generator with nominal rating: equal to or above 80kW.",2]
["A.2","Online UPS 160kVA or higher",1]
["A.3","Shortest exposure time must be 1msec.",2]
["A.4","State the tube current at 150kV.",1]
["A.5","Fluoroscopic programmed and general radiography must be possible for all protocols. Details must be  stated in supporting documents.",1]
["A.6","Auto-setting of all parameters of at least 20 different examinations must be possible.",2]
["A.7","Pulsed fluoroscopy for dose reduction must be available. Details of available Pulse rates (in pulses per second) settings must be stated in supporting documents provided.",2]
["A.8","Self-check of all generator functions must be included.",1]
["A.9","An integrated computerized operator console must be included. ",2]
["A.10","The X-Ray generator and table system must have AEC (Automatic Exposure Control) built into the system.",2]
["A.11","The X-Ray generator must be delivered with a set of matching high tension cables at installation.",1]
["A.12","The X-Ray generator and X-Ray tube unit must have a rapid starter unit ensuring anode rotation of at least 8000 rpm.",1]
["A.13","Details of available radiation reduction software programs and hardware techniques must be provided in supporting documents.",1]
["A.14","An automatic collimator with full field and laser line centering light must be available for the positioning of the patient with full control from the remote table side control and the control room console.",2]
["B","X-Ray Tubes"]
["B.1","X-Ray tube must be supplied synchronized with fixed detector in the table and connected by a C-arm configuration.",2]
["B.2","Dual (1.2 mm and 0.6 mm) focus with ratings compatible with the offered generator must be supplied.",2]
["B.3","Anode material to be tungsten compound with a minimum anode heat storage capacity of at least 600kHU. State anode heat dissipation kHU/min in the supporting documents.",2]
["B.4"," X-Ray tube must have a cooling method. A built-in display screen showing heat status must be provided. Details must be stated in supporting documents provided.",1]
["B.5","Details of  inherent and added filtration must be stated in supporting documents.",1]
["C","Remote Controlled Table"]
["C.1","Remote controlled table  with synchronized flat panel digital detector must be provided.          ",2]
["C.2","Motorized table angulation: +90˚ to -25. Details must be stated in supporting documents.",1]
["C.3","Maximum patient weight limit must be 200kg or more.",2]
["C.4","The table top must be able to move vertically (up and down) for easy patient transfer. The table must have a lockable and adjustable footrest.",1]
["C.5","Table top and mattress provided  must be  radiolucent. Table top dimemsions must be stated",1]
["C.6","Table and tube movement ranges:"]
["C.6.1","State transverse and longitudinal movement.",1]
["C.6.2","The adjustable Source to Image Distance (SID) should be stated. ",1]
["C.6.3","Motorized tube angulation must be stated.",1]
["C.6.4","Controls for table top / X-Ray tube movement must be available at the table side and the remote panel.",2]
["C.6.5","Collision sensors for patient safety must be incorporated within the system.",2]
["C.7","The following table accessories must be included:-"]
["C.7.1","Shoulder rests",1]
["C.7.2","Hand grips",2]
["C.7.3","Foot rest",2]
["C.7.4","Compression band",2]
["C.7.5","Compensation filter pad for peripheral studies",1]
["C.8","Standard extras:"]
["C.8.1","Sialogram (Head lamp)",1]
["C.8.2","HSG lamp",1]
["D","Fixed Detector: Direct Digital Flat Panel. "]
["D.1","A large field direct digital flat panel with a maximum input field of 43 x 43 cm is required. Active detector area: 43 cm by 43 cm (17\" x 17\").",2]
["D.2","Detector matrix dimension must be 2048 x 2048 or greater",1]
["D.3","Detector matrix must be a 16bit pixel depth/Gray scales per pixel.",1]
["D.4","Processor matrix must be 2048 x 2048 or higher.",1]
["E"," Monitors"]
["E.1","Two high resolution TFT LCD  monitors, 21 inch (or latest technology) and height adjustable to be ceiling mounted in the examination room with a movable arm.",2]
["E.2","Two high resolution 21 inch high line-rate TFT LCD monitor to be supplied at the control desk.",2]
["E.3","All four monitors must have a resolution of 1024 x 1024 or higher.",2]
["F","Operator Console"]
["F.1","The system must have a touch screen operator console or equivalent.",2]
["F.2","There must be a built in keyboard with the operator mouse included.",2]
["G","Digital Image Acquisition and Processing System"]
["G.1","Digital acquisition matrix:"]
["G.2","Magnification/Zoom modes must be available. ",1]
["G.3","Single shot exposures must be possible.",2]
["G.4","Last image hold function.Details must be stated in supporting documents.",2]
["G.5","The image storage capacity of hard disk drive must be 2TB or higher.",2]
["G.6","USB port must be enabled/open license (ready for use).",1]
["G.7","Functionality must also include:-"]
["G.7.1","Cine loop display",1]
["G.7.2","Horizontal (R/L) and vertical (up/down) image flip",1]
["G.7.3","Multi-image display format must be possible.",1]
["G.7.4","Digital Subraction Angiography (DSA) ",2]
["G.7.5","Vascular functionality package",2]
["G.7.6","Image review display must include cine loop, playback of sequences at acquisition speed and manual image browsing.",1]
["H","Optional item (Quoted Separately)"]
["H.1","DUAL HEAD HIGH PRESSURE CONTRAST INJECTOR: A dual head contrast injector with saline and contrast injection capabilities is required. Initial 500 lines and 60 syringes should be supplied ",2]
["Total score",null,{"$f":"SUM(C9:C77)","v":86}]
["minimum threshold",null,68]

{"sheet":"3. REMOTE CONTROL TABLE FLUOROS","index":3,"n_rows":85,"n_cols":7,"rows_kept":85,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[83,0,83,1],[84,0,84,1]]}
["                                                              TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 72 out of 91 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item no. 3","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet  /  Any Supporting Document"]
[null,"Remote Control Table Fluoroscopy Screening Unit  with Flat Panel detector (FPD) "]
["A","X-Ray Generator"]
["A.1","Micro-processor controlled high frequency generator with nominal rating: equal to or above 80kW.",2]
["A.2","Online UPS 120kVA or higher",2]
["A.3","The internal  power supply of the system must have an integrated voltage stabilizer. ",1]
["A.4","Shortest exposure time must be 1msec.",2]
["A.5"," State the tube current at 150kV",1]
["A.6","Fluoroscopic programmed and general radiography must be possible for all protocols. Details must be  stated in supporting documents.",1]
["A.7","Auto-setting of all parameters of at least 20 different examinations must be possible.",2]
["A.8","Pulsed fluoroscopy for dose reduction must be available. Details of available Pulse rates (in pulses per second) settings must be stated in supporting documents provided",2]
["A.9","Self-check of all generator functions must be included.",1]
["A.10","An integrated computerized operator console must be included. ",2]
["A.11","The x-ray generator and table system must have AEC( Automatic Exposure Control) built into the system.",2]
["A.12","The x-ray generator must be delivered with a set of matching high tension cables at installation.",1]
["A.13","The x-ray generator and x-ray tube unit must have a rapid starter unit ensuring anode rotation of at least 8000 rpm.",1]
["A.14","Details of available radiation reduction software programs and hardware techniques (copper filters or grids) must be provided in supporting documents.",1]
["A.15","An automatic collimator with full field and laser line centering light must be available for the positioning of the patient with full control from the remote table side control and the control room console ",2]
["A.16","The generator must accommodate two (2) X-Ray tubes (Fluroscopy & overhead tube).",2]
["B","Two X-Ray Tubes"]
["B.1","Two  X-Ray tubes must be supplied. One X-Ray tube is synchronized with fixed detector in the table, while the second (overhead) X-Ray tube is connected  as a ceiling suspended X-Ray tube with erect Bucky.",2]
["B.2","Dual focus with ratings compatible with the offered generator must be supplied: "]
["B.2.1","Dual (1.2 mm and 0.6 mm) focus with ratings compatible with the offered generator must be supplied.Large focus to be 1.2 mm ",2]
["B.3","Anode material to be tungsten compound with a minimum anode heat storage capacity of at least 600kHU. State anode heat dissipation kHU/min in the supporting documents.",2]
["B.4"," X-Ray tube must have a cooling method. A built-in display screen showing heat status must be provided. Details must be stated in supporting documents provided.",1]
["B.5","Details of  inherent and added filtration must be stated in supporting documents.",1]
["C","Remote Controlled Table"]
["C.1","Remote controlled table  with synchronized flat panel digital detector and X-Ray tube must be provided.          ",2]
["C.2","Motorized table angulation: +90˚ to -25˚. Details must be stated in supporting documents.",2]
["C.3","Maximum patient weight limit must be 200kg or more.",2]
["C.4","The table top must be able to move vertically (up and down) for easy patient transfer. The table must have a lockable and adjustable footrest.",1]
["C.5","Table top and mattress provided  must be  radiolucent. Table top dimemsions must be stated",1]
["C.6","Table and tube movement ranges:"]
["C.6.1","State transverse and the longitudinal movement.",1]
["C.6.2"," The adjustable Source to Image Distance (SID) should be stated. ",1]
["C.6.3","Controls for table top / X-ray tube movement must be available at the table side and the remote panel",2]
["C.6.4","Collision sensors for patient safety must be incorporated within the system.",2]
["C.7","The following table accessories must be included:-"]
["C.7.1","Shoulder rests",1]
["C.7.2","Hand grips",2]
["C.7.3","Foot rest",2]
["C.7.4","State compression device",1]
["C.7.5","Compensation filter pad for peripheral studies",1]
["C.8","Standard extras:"]
["C.8.1","A wireless  Cesium Iodide, amorphous silicon type digital flat panel detector  of size  35 cm x 43cm or 43cm x 43cm , must be included as a standard. ",2]
["C.8.2","Flat panel detector radioluscent protector, must be included in the pricing.",1]
["C.8.3","Head lamp ( Sialogram exam)","1"]
["C.8.4","Fixed or mobile lamp (HSG exams) ","1"]
["C.8.5","A wall mounted hanger/cabinet for the storage of wireless detector must be included in the offer.",1]
["D","Fixed Detector: Direct Digital Flat Panel. "]
["D.1","A large field direct digital flat panel with a maximum input field of 43 x 43 cm is required. Active detector area: 43 cm by 43 cm (17\" x 17\").",1]
["D.2","Detector matrix dimension must be 2048 x 2048 or greater",1]
["D.3","Detector matrix must be a 16bit pixel depth/Gray scales per pixel.",1]
["D.4","Processor matrix must be 2048 x 2048 or higher.",1]
["E","TV Monitors"]
["E.1","Two high resolution TFT LCD  monitors, 21 inch (or latest technology) and height adjustable to be ceiling mounted in the examination room with a movable arm.",2]
["E.2","Two high resolution 21 inch high line-rate TFT LCD monitor to be supplied at the control desk.",2]
["E.3","All four monitors must have a resolution of 1024 x 1024 or higher.",2]
["F","Operator Console"]
["F.1","The system must have a touch screen operator console.",2]
["F.2","There must be a built in keyboard with all the operating features applicable to the system.",2]
["G","Digital Image Acquisition and Processing System"]
["G.1","Digital acquisition matrix:"]
["G.2","Magnification/Zoom modes must be available. ",1]
["G.3","Single shot exposures must be possible.",2]
["G.4","Last image hold function.Details must be stated in supporting documents.",2]
["G.5","The image storage capacity of hard disk drive must be 2TB or higher.",2]
["G.6","USB port must be enabled/open license (ready for use).",1]
["G.7","Functionality must also include:-"]
["G.7.1","Cine loop display",1]
["G.7.2","Horizontal (R/L) and vertical (up/down) image flip",1]
["G.7.3","Multi-image display format must be possible.",1]
["G.7.4","Split display for reference image comparison on the second monitor ",1]
["G.7.5","Digital Subraction Angiography (DSA) ",2]
["G.7.6","Vascular functionality package",2]
["G.7.7","Image review display must include cine loop, playback of sequences at acquisition speed and manual image browsing.",1]
["H","Optional item (Quoted Separately)"]
["H.1","DUAL HEAD HIGH PRESSURE CONTRAST INJECTOR: A dual head contrast injector with saline and contrast injection capabilities is required. Initial 500 lines and 60 syringes should be supplied ",2]
["TOTAL ",null,{"$f":"SUM(C8:C83)","v":91}]
["MIN THRESHOLD ",null,72]

{"sheet":"4. DIGITAL FLAT PANEL","index":4,"n_rows":64,"n_cols":7,"rows_kept":64,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[6,0,6,1],[7,1,7,6],[62,0,62,1],[63,0,63,1]]}
["                                                              TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 50 out of 62 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item No.4","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["Two x Flat Panel Detectors, Direct, Digital, Wireless, Portable, High Capacity with a Portable Operater's Consoles "]
["A","General"]
["A.1","Two portable and wireless, high capacity, direct digital flat panel, battery-powered detectors with a portable operator's console for each must be  provided: Active imaging size must be: \na. 24cm x 30cm                                                                                                                                                                                                                                                                                                                                                                                      b.43cm x 43cm. \nThe effective/active sizes and dimensions must be stated for both detector sizes. Bidders to offer an option of buying the detectors separately.",2]
["A.2","A wall mounted detector cabinet for the storage of wireless detectors must be included in the offer",1]
["A.3","The offered detectors must be configured to actively and optimally function with any general X-Ray rooms at no additional cost to the end-user. Provide the details of the interconnection configurations.",2]
["B ","Wireless Flat Panel Detectors"]
["B.1","The equipment offered must have a high shock tolerance and water resistant. Provide the details of the safety and protective features for each detector. ",2]
["B.2","The equipment must be offered with a radiolucent shock resistant protective cover. Provide the details of the material and durability of the covers. ",2]
["B.3","The offer must include two light weight, shock resistant, hardbody carry cases with sponges and wheels to protect the equipment during transport to the wards. Each carry case must fit one detector and console as well as an additional battery. The bidder must give an option of buying this item separately as and when required.",1]
["B.4","Image transfer must be done as follows (to the console): "]
["B.4.1","Wireless communication (WI-FI) & LAN must be enabled. State other available latest modes of image transfer.",2]
["B.4.2","Systems must have both 2.4GHz and 5GHz wireless transmission.",1]
["B.5","A. 43cm x 43cm flat panel detector: "]
["B.5.1","The scintillator must be Amorphous silicon photodiode.",2]
["B.5.2","The battery provided must be lithium or better. ",1]
["B.5.3","Pixel size/pitch must be 140 micrometer (µm) or smaller. ",1]
["B.5.4","The acquisition and digital conversion of the image from the flat panel of 14-bit or more. Details must be stated in the supporting documents provided . ",1]
["B.5.5","The image resolution must be at least 3.5 line pairs/mm. Details are stated in the supporting documents provided. ",1]
["B.5.6","The sytem must accept a minimum of 40kVp - 150 kVp.",1]
["B.5.7","The preview display time must  be 5 seconds or less. Details are stated in the supporting documents provided. ",2]
["B.5.8","The full image cycle time should be a maximum of 10 seconds.Details are stated in the supporting documents provided . ",2]
["B.5.9","The detector must be able to store a minimum of 100 images in the internal memory. The internal panel image storage capacity must be stated in the supporting documents.",1]
["B.5.10","The uniform load that the detector must be able to withstand should be at least 150kg. Details are stated in the supporting documents provided . ",1]
["B.5.11","The local load (on an area of 40 mm diameter)  that the detector must be able to withstand should be at least 100kg. Details are stated in the supporting documents provided .",1]
["B.6","24cm x 30cm flat panel detector: "]
["B.6.1","The scintillator must be Amorphous silicon photodiode.",2]
["B.6.2","The battery provided must be lithium or better. ",1]
["B.6.3","Pixel size/pitch must be 140 micrometer (µm) or smaller. ",1]
["B.6.4","The acquisition and digital conversion of the image from the flat panel of 14-bit or more. Details must be stated in the supporting documents provided . ",1]
["B.6.5","The image resolution must be at least 3.5 line pairs/mm. Details are stated in the supporting documents provided. ",1]
["B.6.6","The sytem must accept a minimum of 40kVp - 150 kVp.",1]
["B.6.7","The preview display time must  be 3 seconds or less. Details are stated in the supporting documents provided. ",2]
["B.6.8","The full image cycle time should be a maximum of 6 seconds.Details are stated in the supporting documents provided . ",2]
["B.6.9","The detector must be able to store a minimum of 100 images in the internal memory. The internal panel image storage capacity must be stated in the supporting documents.",1]
["C","Battery"]
["C.1","The following battery charger must be included for each detector:"]
["C.1.1","Four rechargeable batteries, two per detector must be provided. The battery should be able to handle 5 hours of active use when fully charged. Provide details of battery activity durations. ",2]
["C.1.2","Multi-slot charger to be provided. ",2]
["C.1.3","Charging time for each battery from fully depleted to fully charged should be less than 6 hours.",1]
["C.1.4","The rated power input must be: 220 - 240V AC, 50Hz, single phase.",2]
["D","Grid "]
["D.1","An encasement with a built in grid that fits the 24cm x 30cm or 43cm x 43cm detector must be supplied.  ",1]
["D.2","The grid must have at least:"]
["D.2.1","Grid ratio 8:1",1]
["D.2.2","Must be usable with FFD of 100cm to 180cm ",1]
["E","Operator's Console - Acquisition and Image Processing View Station"]
["E.1","The operator's console must be portable laptop with the latest operating software (iCore 7 or better).",2]
["E.2","A protective casing/bag for the operator's console must be included.",1]
["E.3","The operator's console must connect wirelessly to PACS/RIS/Printer.",1]
["E.4","The operator's consoles must be touch screens for user interface. Type of screen and user interface is stipulated in the supporting documents provided.",2]
["E.5","Print option to a DICOM DRY LASER printer must be possible.",2]
["E.6","The DICOM Modality Work list must be displayed on the screen and form part of the workflow.The worklist must allow for the display of examinations scheduled and performed and must reflect the date, time and patient details of each examination. It must also be available as a global network query. Details are stated in the supporting documents provided. ",1]
["E.7","The equipment must connect to RIS and PACS wirelessly and must be able to receive patient demographics from the RIS. ",1]
["E.8","It must be possible to enter all patient data and demographics manually in the event that the RIS is unavailable.",1]
["E.9","Image post-processing tools must be included. Details of post-processing tools must be stated.                                                                                                                                                                                                                                                                                           ",1]
["E.10","Exposure factors must be displayed on the screen. Details are stated in supporting documents provided.",1]
["TOTAL ",null,{"$f":"SUM(C8:C62)","v":62}]
["MIN THRESHOLD ",null,50]

{"sheet":"5. PANELIPSE DIGITAL","index":5,"n_rows":36,"n_cols":7,"rows_kept":36,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[10,5,10,6],[34,0,34,1],[35,0,35,1]]}
["                                                              TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 32 out of 39 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item No.5","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["A","Panelipse Digital"]
["A.1","The unit must be able to perform digital panoramic and cephalic imaging of the upper and lower jaw in multiple planes. ",2]
["A.2","The unit must have a software or system capable of performing pan tomography exam and automatically removing redundant tomographic shadows that result in geometric unsharpness. Details of software package are stated in supporting documents provided.",2]
["A.3","The unit must allow for pre-programmed settings, but also manually selectable exposures, for children and adults of  different sizes. Details are stated in supporting documents provided.",2]
["A.4","The unit must have an automatic double TMJ program to perform full temporo-mandibular studies on a single display or film. Details are stated/displayed in supporting documents provided.",1]
["A.5","The unit must be capable of performing image segmenting to reduce radiation, e.g. vertical segmenting to expose a smaller area of diagnostic interest. Details are stated in supporting documents provided.",1]
["A.6","The unit must be able to perform the exact, immediate positioning of the anterior teeth in the focal layer.",2]
["A.7","The unit must have following functions; Central control, motorized, height adjustment, forehead and temple supports. Details of where motorized chin controls are located must be stated/displayed1 in supporting documents provided.",1]
["A.8","The unit must have Bite Guide/Chin Rest with adaptable anterior position adjustment for both adult and children.  Details on applicability of chin rest for adults and children,  are stated/displayed in supporting documents provided.",2]
["A.9","The unit must have a fixed bite block which is easy to clean after each patient.",2]
["A.10","The unit must have hand grips for both hands and head for immobilization.",2]
["A.11","The unit must have a patient mirror to assist with accurate positioning. Details are stated/displayed in supporting documents provided.",2]
["A.12","The unit must have laser alignment lights to accurately guide patient positioning.",2]
["A.13","The unit must have a touch screen with annotative text and/or graphic symbols.",2]
["A.14","The unit must display all patient work list information  on the main console.",1]
["A.15","The unit must be equipped with a self-diagnostic test system, capable of displaying error messages/codes. ",1]
["A.16","The unit must incorporate a fully automatic film marking system for panoramic radiography to mark the exposure factors, the chosen program, as well as patient identification information.",1]
["A.17","The unit's floor side stands/mounting must be able to accommodate patients in wheelchairs. Details are stated/displayed in supporting documents provided.",2]
["A.18","The unit must have power consumption of the unit must be 2.5kW or above. Details are stated in supporting documents provided.",1]
["A.19","The unit must have total tube filtration of 2.5mm aluminium/copper. Details are stated/displayed in supporting documents provided.",1]
["A.20","The unit must have anode voltage to be from 40kVp to 90 kVp. Details are stated in supporting documents provided. ",1]
["A.21","The unit must have tube anode current to be from 1-16mA. Details are stated in supporting documents provided.",1]
["A.22","The unit must have an exposure time of 2.7 to 20 seconds continuous or split.",1]
["A.23","UPS in line (in series connection to main power supply)/Online (uninterruptable power supply unit) for the workstation,  must be included. Details are stated/displayed in supporting documents provided.",2]
["A.24","The internal  power supply of the system must have an integrated voltage stabilizer. ",1]
["B","System Connectivity"]
["B.1","19 inch or better, touch screen, LCD monitor must be provided with the operating system (iCore 7 or better)",2]
["B.2","The unit must have a minimum RAM of 4GB and minimum hard disk memory of  500GB.",1]
["Total Points",null,{"$f":"SUM(C8:C34)","v":39}]
["Minimum threshold ",null,31]

{"sheet":"6. CT SCANNER 128-SLICE (2)","index":6,"n_rows":90,"n_cols":7,"rows_kept":90,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[6,0,6,1],[88,0,88,1],[89,0,89,1]]}
["                                                           ANNEXURE A: TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 76 out of 96 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item No.6","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["128 Slice CT Scanner with Dual Head Automatic Contrast Injector"]
["A","A  DICOM 3 compatible multi slice detector CT system for 128 slice per rotation, must be supplied. Supports whole body CT scanning including whole body angiography",2]
["A.1","Gantry:"]
["A.1.1","The gantry aperture must be equal or greater than 70cm",2]
["A.1.2","It must be possible to scan either Head First or Feet First.",2]
["A.1.3","Rotation time range from 0.2 sec - 1.5 sec  at full rotation (360 degrees)",1]
["A.1.4"," scan speed must be 0.5 seconds or less at 360 degrees. ",1]
["A.1.5","The standard Field of View must be equal or greater than 50cm",2]
["A.1.6","Emergency stop switches must be available on the gantry as well as the console.",2]
["A.1.7","2-way intercom from operator console to gantry must be provided.",2]
["A.1.8","CT fluoroscopy functionality, must be provided as part of the tender. The CT Fluoroscopy mode should have images displayed in real time.",2]
["A.1.9","A viewing monitor inside the scanning room must be provided for use during CT fluoroscopy examinations.",2]
["B","X-Ray Generator"]
["B.1","An  output  in the range between 80kW-100kW is required.",2]
["B.2","System should have a maximum output of 140kV.",2]
["B.3","System must have (tube current) mA minimum  range between 10mA to 40mA and maximum range between 800mA to 1400mA. ",2]
["C","X-Ray Tube"]
["C.1","Anode heat storage capacity must be 7 MHU and above.",1]
["D","Detector system:"]
["D.1","Detectors must be of solid state design. Details of detector are stated in supporting documents.",2]
["D.2","Detector geometric efficiency must be at least 80% for all modes of operation and at least from 90% absorption efficiency. ",2]
["E","Patient Table"]
["E.1","Loading capacity of standard table 200kg and above. Details of the weight tolerance parameters must be stated. ",1]
["E.2","Lowest vertical table height must range between 30cm-55 cm (distance from the floor).",1]
["E.3","The table width must be 45cm or wider",1]
["E.4","A longitudinal scannable and Scout view range of 170cm and above must be achievable, for head to foot anatomical coverage. ",1]
["E.5","The unit must have dual controls for the table movement on the gantry. Table movement must be possible on the radiographer's console.",1]
["E.6","The following accessories must be included as a standard:"]
["E.6.1","Head holders",1]
["E.6.2","Immobilization straps and cushions",1]
["E.6.3","Knee support",1]
["E.6.4","Infant Immobiliser/cradle with cushion",2]
["E.6.5","Radioluscent Mattress. Must be removable and easy to clean",1]
["E.6.6","Leg extender with cushion",1]
["E.6.7","Flat Head holder cushion",1]
["E.6.8","Patient straps ",1]
["E.6.9","Patient transfer board ",2]
["G","Operators Console:"]
["G.1","A workstation with two x 19 inch or better high resolution Flat Screen LCD diagnostic colour monitors with keyboards and mouse must be provided. The Monitors must be 1.3MP or above",2]
["G.2","Image storage capacity on internal hard drive  must be 2TB or bigger. Details of archive extension possibilities are stated in supporting documents as optional items",2]
["G.3"," 32GB RAM and above is required.Details are stated in supporting documents",1]
["G.4","iCore 7 Microprocessor",1]
["G.5","Anti Virus software to be installed (and auto-updateable). All updates must to be in the warranty and maintenance cover.",2]
["G.6","Four Adjustable ergonomic office chair with wheels.The chair must accomodate a weight of up to 120kg. ",2]
["G.7","Performance (All specifications to be applicable to sub-second scan mode):"]
["G.7.1","Spatial resolution must be stated in lp/mm and must be stated in terms of a CT phantom (supplied with the scanner). The resolution must be the same in the x, y and z directions. Bidders are to confirm that the resolution is the same in all 3 planes.  ",2]
["G.7.2","A dose reduction mechanism for a 128 slice CT Scanner(including software), that are included in the standard package must be stated. ",2]
["H","Scanning Modes"]
["H.2","Volume scan mode"]
["H.2.1","It must be possible to perform multiple scan sequences.",1]
["H.2.2","Iterative reconstruction algorithm should be offered.",2]
["H.2.3","The interscan delay between one helical and the next may not exceed 5 seconds.",1]
["H.2.4","Optimal bolus concentration must be possible. A software package for bolus tracking should be included  as a standard.",1]
["J","Radiologist Console:"]
["J.1","Two doctors workstations with a minimum 3 MP 19 inch or better reporting monitor must be linked to the main system and have their own independent consoles, allowing viewing, post processing and filming.  ",2]
["J.2","Image transfer must occur in the background, without causing a bottleneck and interfering with other functions - must be Dicom 3 compatible.",1]
["J.3","The workstations must include software for viewing, Cine mode MPR, 3D and Volume Rendering. All software packages included in the pricing must be stated.   ",2]
["J.4","The Following Software/Hardware functions must be included in the offer:"]
["J.4.1","Vascular: 3D surface analysis packages for CT angiography with following functions:",1]
["J.4.2","MPVR",1]
["J.4.3","MPR",1]
["J.4.4","Image addition and subtraction",1]
["J.4.5","MIPS and MinIP ",1]
["J.4.6","Disarticulation Software.",1]
[]
["J.5","Oncology Software Package:"]
["J.5.1","Tumor detection, evaluation and follow up, for example, with CAD and tumor volume evaluation.",1]
["J.5.2","CT FLUOROSCOPY: To perform interventional is required, including the ability to interactively change table height, longitudinal table position. ",2]
["J.5.3","3D Intervention software package.",2]
["J.5.4","3D-guided intervention and full table-side scanner control. ",2]
["J.5.5","CARDIAC PACKAGE: A comprehensive Cardiac Package is required. ECG, calcium scoring, gating scanning, ECG gated reconstruction hardware and software as well as the patient trigger must be available on the CT Scanner. Full details are to be supplied on the workstation",2]
["J.5.6","NEURO DSA: Neuro DSA software package to be available.  State functionality of standard package and available options.",2]
["J.5.7","PERFUSION PACKAGE: Brain perfusion package must be offered . State functionality of standard package and available options.",2]
["J.5.8","DUAL HEAD HIGH PRESSURE CONTRAST INJECTOR: A dual head contrast injector with saline and contrast injection capabilities is required. Initial 500 lines and 60 syringes should be supplied ",2]
["J.5.9","Online UPS 120kVA or higher",2]
["J.5.10","Three airconditioners should be supplied:"]
["J.7.10.1","18000BTU for the control room. Details of the airconditioners should be stated."]
["J.7.10.2"," 32000BTU for the CT room. Details of the airconditioners should be stated."]
["J.7.10.3","32000BTU for the UPS. Details of the airconditioners should be stated.",2]
["J.7.10.4","Optional items (quoted separately)"]
["J.7.10.5","Dental Function and Hardware.",1]
["J.7.10.6","Virtual colonoscopy package function and hardware ",1]
["Total Score",null,{"$f":"SUM(C8:C88)","v":96}]
["Minimum Threshold",null,"76"]

{"sheet":"7. CT SCANNER 256-SLICE","index":7,"n_rows":88,"n_cols":7,"rows_kept":88,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[6,0,6,1],[86,0,86,1],[87,0,87,1]]}
["                                                           ANNEXURE A: TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 80 out of 100 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item No.7","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["256 Slice CT Scanner with Dual Head Automatic Contrast Injector"]
["A","A  DICOM 3 compatible multi slice detector CT system for 256 slice per rotation, must be supplied. Supports whole body CT scanning including whole body angiography",2]
["A.1","Gantry:"]
["A.1.1","The gantry aperture must be equal or greater than 70cm",2]
["A.1.2","It must be possible to scan either Head First or Feet First.",2]
["A.1.3","Rotation time range from 0.2 sec - 1.5 sec  at full rotation (360 degrees)",1]
["A.1.4"," scan speed must be 0.5 seconds or less at 360 degrees. ",1]
["A.1.5","The standard Field of View must be equal or greater than 50cm",2]
["A.1.6","Emergency stop switches must be available on the gantry as well as the console.",2]
["A.1.7","2-way intercom from operator console to gantry must be provided.",2]
["A.1.8","CT fluoroscopy functionality, must be provided as part of the tender. The CT Fluoroscopy mode should have images displayed in real time.",2]
["A.1.9","A viewing monitor inside the scanning room must be provided for use during CT fluoroscopy examinations.",2]
["B","X-Ray Generator"]
["B.1","An  output  in the range between 80kW-100kW is required.",2]
["B.2","System should have a maximum output of 140kV.",2]
["B.3","System must have (tube current) mA minimum  range between 10mA to 40mA and maximum range between 800mA to 1400mA. ",2]
["C","X-Ray Tube"]
["C.1","Anode heat storage capacity must be 7 MHU and above.",1]
["D","Detector system:"]
["D.1","Detectors must be of solid state design. Details of detector are stated in supporting documents.",2]
["D.2","Detector geometric efficiency must be at least 80% for all modes of operation and at least from 90% absorption efficiency. ",2]
["E","Patient Table"]
["E.1","Loading capacity of standard table 200kg and above. Details of the weight tolerance parameters must be stated. ",1]
["E.2","Lowest vertical table height must range between 30cm-55 cm (distance from the floor).",1]
["E.3","The table width must be 45cm or wider",1]
["E.4","A longitudinal scannable and Scout view range of 170cm and above must be achievable, for head to foot anatomical coverage. ",1]
["E.5","The unit must have dual controls for the table movement on the gantry. Table movement must be possible on the radiographer's console.",1]
["E.6","The following accessories must be included as a standard:"]
["E.6.1","Head holders",1]
["E.6.2","Immobilization straps and cushions",1]
["E.6.3","Knee support",1]
["E.6.4","Infant Immobiliser/cradle with cushion",2]
["E.6.5","Radioluscent Mattress. Must be removable and easy to clean",1]
["E.6.6","Leg extender with cushion",1]
["E.6.7","Flat Head holder cushion",1]
["E.6.8","Patient straps ",1]
["E.6.9","Patient transfer board ",2]
["G","Operators Console:"]
["G.1","A workstation with two x 19 inch or better high resolution Flat Screen LCD diagnostic colour monitors with keyboards and mouse must be provided. The Monitors must be 1.3MP or above",2]
["G.2","Image storage capacity on internal hard drive  must be 2TB or bigger. Details of archive extension possibilities are stated in supporting documents as optional items",2]
["G.3"," 32GB RAM and above is required.Details are stated in supporting documents",1]
["G.4","iCore 7 Microprocessor",1]
["G.5","Anti Virus software to be installed (and auto-updateable). All updates must to be in the warranty and maintenance cover.",2]
["G.6","Four Adjustable ergonomic office chair with wheels.The chair must accomodate a weight of up to 120kg. ",2]
["G.7","Performance (All specifications to be applicable to sub-second scan mode):"]
["G.7.1","Spatial resolution must be stated in lp/mm and must be stated in terms of a CT phantom (supplied with the scanner). The resolution must be the same in the x, y and z directions. Bidders are to confirm that the resolution is the same in all 3 planes.  ",2]
["G.7.2","A dose reduction mechanism for a 256 slice CT Scanner(including software), that are included in the standard package must be stated. ",2]
["H","Scanning Modes"]
["H.1","Volume scan mode"]
["H.1.1","It must be possible to perform multiple scan sequences.",1]
["H.1.2","Iterative reconstruction algorithm should be offered.",2]
["H.1.3","The interscan delay between one helical and the next may not exceed 5 seconds.",1]
["H.1.4","Optimal bolus concentration must be possible. A software package for bolus tracking should be included  as a standard.",1]
["J","Radiologist Console:"]
["J.1","Two doctors workstations with a minimum 3 MP 19 inch or better reporting monitor must be linked to the main system and have their own independent consoles, allowing viewing, post processing and filming.  ",2]
["J.2","Image transfer must occur in the background, without causing a bottleneck and interfering with other functions - must be DICOM 3 compatible.",1]
["J.3","The workstations must include software for viewing, Cine mode MPR, 3D and Volume Rendering. All software packages included in the pricing must be stated.   ",2]
["J.4","The Following Software/Hardware functions must be included in the offer:"]
["J.4.1","Vascular: 3D surface analysis packages for CT angiography with following functions:",1]
["J.4.2","MPVR",1]
["J.4.3","MPR",1]
["J.4.4","Image addition and subtraction",1]
["J.4.5","MIPS and MinIP ",1]
["J.4.6","Disarticulation Software.",1]
["J.6","Oncology Software Package:"]
["J.6.1","Tumor detection, evaluation and follow up, for example, with CAD and tumor volume evaluation.",1]
["J.6.2","CT FLUOROSCOPY: To perform interventional is required, including the ability to interactively change table height, longitudinal table position. ",2]
["J.6.3","3D Intervention software package.",2]
["J.6.4","3D-guided intervention and full table-side scanner control. ",2]
["J.6.5","CARDIAC PACKAGE: A comprehensive Cardiac Package is required. ECG, calcium scoring, gating scanning, ECG gated reconstruction hardware and software as well as the patient trigger must be available on the CT Scanner. Full details are to be supplied on the workstation",2]
["J.6.6","NEURO DSA: Neuro DSA software package to be available.  State functionality of standard package and available options.",2]
["J.6.7","PERFUSION PACKAGE: Brain perfusion package must be offered . State functionality of standard package and available options.",2]
["J.6.8","DUAL HEAD HIGH PRESSURE CONTRAST INJECTOR: A dual head contrast injector with saline and contrast injection capabilities is required. Initial 500 lines and 60 syringes should be supplied ",2]
["J.6.9","Online UPS 200kVA or higher",2]
["J.6.10","18000BTU for the control room. Details of the airconditioners should be stated.",2]
["J.6.11"," 32000BTU for the CT room. Details of the airconditioners should be stated.",2]
["J.6.12","32000BTU for the UPS. Details of the airconditioners should be stated.",2]
["K",""]
["K.1","Dental Function and Hardware.",1]
["K.2","Virtual colonoscopy package function and hardware ",1]
["Total Score",null,{"$f":"SUM(C8:C86)","v":100}]
["Minimum Threshold",null,"80"]

{"sheet":"8. MRI 1,5T","index":8,"n_rows":189,"n_cols":7,"rows_kept":189,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[6,0,6,6],[8,1,8,4],[22,1,22,4],[26,1,26,4],[39,1,39,4],[52,1,52,4],[84,1,84,4],[86,1,86,4],[100,1,100,4],[155,1,155,4],[166,1,166,4],[168,1,168,4],[187,0,187,1],[188,0,188,1]]}
["ANNEXURE A: TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 180 out of 225 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item No 8","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet  /  Any Supporting Document"]
["MRI 1.5 Tesla"]
["A"," Modality Details"]
["A.1","MAGNET"]
["A.1.1","The Magnet Field Strength shall be at least 1.5 Tesla active shielded.",2]
["A.1.2","The Magnet must be closed bore cylindrical type and design.",2]
["A.1.3","Bore length including all covers must  be a minimum of 140cm and not exceed 180cm.",1]
["A.1.4","The internal bore size must not be less than 70cm inner magnet. State the dimensions (L x W x H). ",1]
["A.1.5","Magnet homogeneity should meet the following specifications using the standard deviation VRMS (volume root-meansquare) using 24 plane plot measurement method. Provide the actual values of the magnet homogeneity. "]
["A.1.5.1","50 cm DSV (Diameter Spherical Volume) state (0.8 - 5.0 ppm)",1]
["A.1.5.2","40 cm DSV state (0.2 - 1.0 ppm)",1]
["A.1.5.3","30 cm DSV state (0.05 - 0.25 ppm)",1]
["A.1.5.4","20 cm DSV state (0.01 - 0.06 ppm)",1]
["A.1.5.5","10 cm DSV  state (0.002 - 0.017 ppm)",1]
["A.1.5.6","Magnetic field stability shall be less than 0.1 ppm/hour.",1]
["A.1.5.7","The 5 Gauss/0.5mT fringe field must be contained in an area of radial and axial of 3-5m.  State actual area.",1]
["A.1.5.8","The minimum helium boil off rate should be less than 0.02 ltr/hr under normal operating conditions",1]
["B","MAGNET SAFETY"]
["B.1","Magnet must be equipped with quench exhaust leading to the outside of the building in event of Magnet quench to prevent injury to staff and patient/depending on type of cooling system available. State technology, vent pipe requirements (where applicable). ",2]
["B.2","Magnet must be equipped with emergency ramp down unit for fast Magnetic reduction and ramp up procedure, state details.",2]
["B.3","MRI Signage/Floor Sticker Warning Signs/MRI Symbols Sign/ MRI Zone Signs, “Do Not Enter” Floor Cones must be provided (Complete set).",2]
["C","GRADIENT SYSTEM (Provide advanced or latest technology details)"]
["C.1","Actively shielded hi-performance non-resonant gradient coil system must be supplied.",2]
["C.2","Gradient amplitude/peak strength must be at least 33mT/m measured per real axis plateau (100% duty cycle) not effective gradients: Sate options of highest gradients/Higher gradients will be an advantage.",1]
["C.3","Gradient duty cycle must be 100%.",1]
["C.4","Gradient rise time from 0 to maximum gradient amplitude must be 200 micro-seconds or more.",1]
["C.5","Gradient slew rate must be 120 m/mT/ms or more measured per real axis plateau, not effective values. Provide the data sheet/brochure of the slew rates parameters.",1]
["C.6","Scan matrix must be minimum of 1024 x 1024 or better. Maximum recon matrix must be stated.",1]
["C.7","The reconstruction speed at 100% FOV must not be less than 60 000 reconstructions /sec.",1]
["C.8","Gradient upgrades to different levels should be possible without changing gradient coil. State the details of the available upgrade for the gradient.",1]
["C.9","The system must have the gradient coil cooling system. Provide the details of the cooling system offered.  ",1]
["C.10","The output linearity of the gradient amplifiers should be maximum of  0.1% of peak.",1]
["C.11","The unit must have acoustic noise reduction mechanisms/system for all patients (adults & paediatrics).   ",1]
["C.12","Free choice of flip angle while maintaining signal to noise ratio to be supported. ",1]
["D","RADIOFREQUENCY SYSTEM"]
["D.1","Resonance frequency must be 63.86MHz or 1.5 Tesla. ",1]
["D.2","Direct Radio Frequency (RF) Transmitter System: Digital signal generation and processing must be possible. ",1]
["D.3","The transmission system must be integrated in the magnet housing.",1]
["D.4","Power output of transmitter amplifier rating must be 18kW or better.",1]
["D.5","The system must be equipped with RF fault protection limiting RF output in event of malfunction.",1]
["D.6","The receiver components must be integrated into the magnet housing.",1]
["D.6.1","Phased array acquisition system with minimum of 16 independent digital RF receiver channels or more must be supplied. State commercial available channel upgrade path and commercial available coils utilizing the number of channels. ",1]
["D.6.2","The system should have at least 32 independent RF receiver channels or better. ",1]
["D.6.3","Phase resolution shall be 0.1 degree/bit or better",1]
["D.6.4","Noise of the preamplifier to be less or equal to 0.5 decibels",1]
["D.7","The Digital receiver and transmitter amplitude must be 16 bit control or more.",1]
["D.8","All coil elements must be used seamlessly  in one study without coil changes and without repositioning of the patient. State maximum number of simultaneously connected coil elements.",1]
["E","RF COILS"]
["E.1","The bidder must supply market related Integrated Coil Technology. State how the Coil technology of the unit contributes and improve the Image Quality and Workflow. ",1]
["E.2","Integrated circular polarised/quadrature transmit and receive body coil.",1]
["E.3","It must be possible to select active coil or elements from the main console.",1]
["E.4","Standard coils for the following applications should be available with  the system:"]
["E.4.1","Body (Chest, abdomen, pelvis).",1]
["E.4.2","Head ",1]
["E.4.3","Whole spine.",1]
["E.4.4","Extremities and joints: wrist, hips, shoulder,  knee,  foot/ankle,",1]
["E.4.5","Breast MR. ",1]
["E.4.6","Whole body vascular and Peripheral vascular array.",1]
["E.4.7","Dedicated pediatric coils.",1]
["E.4.8","Supply an MRI compatable cabinet in the room for storage of all coils and other accessories.",2]
["E.4.9","Coils to facilitate optimal facial, calvarial and intracranial imaging in the child from 1.5-60kgs, including visualisation of the orbits, optic nerves, optic tracts, pituitary fossa, hypothalamus, temporal lobe, posterior fossa and cerebral cortex. Coils to provide optimal imaging including, but not limited to the clinical settings.",1]
["F","PATIENT SUPPORT/TABLE and MANAGEMENT/ PATIENT COMFORT"]
["F.1","Two dockable tables or a trolley with a fixed table must be provided and included in the total price",2]
["F.2","Dual table control panels shall be located at either side of aperture/gantry for easy access. State if controls are available on the rear of the magnet.",2]
["F.3","Centering  laser light beams for anatomical references.",1]
["F.4","Table movement shall be controlled from both gantry and operator console.",2]
["F.5","Patient table shall be equipped with manual override for quick removal of patient from the magnet-bore in case of emergency.",2]
["F.6","Maximum load must be  minimum of 140kg or better. State actual maximum load.",1]
["F.7","The following table movement functions must be possible:"]
["F.7.1","Accuracy of repositioning to last scan position.",1]
["F.8","Physiologic measurement unit essential with display of ECG, respiration and pulse at the main console and gantry.",2]
["F.9","Two way in-bore intercom system shall allow communication with patient while gradient is running.",2]
["F.10","Hand held alarm button for patient signalling.",2]
["F.11","Table restraining/immobilization straps are required per table.",2]
["F.12","Integrated music for patient shall be included.",1]
["F.13","Variable patient comfort lighting/ambience to be included.",1]
["F.14","MRI compatible sand bags and sponges in various sizes and shapes.",2]
["F.15","Ventilation in the gantry /Fresh air supply.",2]
["F.16","Auto-voice system.",1]
["G"," WORKSTATION: DOCTORS CONSOLE"]
["G.1","Two doctors workstations with a minimum 3 MP 19 inch or better reporting monitor  with touch screen must be linked to the main system and have their own independent consoles, allowing viewing, post processing and archiving.  ",2]
["H","OPERATOR USER INTERFACE"]
["H.1","Two 19 inch with touch screen or larger hi-resolution colour LCD flat-panel flicker-free monitor with undistorted image display required or better.",1]
["H.2","Resolution of the monitor must be 1024 x 1024 pixel or better",1]
["H.3","User interface providing flexible multi-tasking in foreground or background (scanning, filming, reconstruction).",2]
["H.4","6 TB external hard drive as storage devices required.",1]
["H.5","All standard image processing features are required in addition to the following advanced features must be available:"]
["H.5.1","Multi-planner reformatting (MPR).",1]
["H.5.2","Multi-projection volume rendering (MPVR).",1]
["H.5.3","Maximum intensity projection (MIP).",1]
["H.5.4","MR Angiography processing.",1]
["H.5.5","3D surface rendering.",1]
["H.5.6","MR Hydrography MRCP/Urography/Myelography.",1]
["H.5.7","Image add/subtract.",1]
["H.5.8","CT image display and intergration",1]
["I","ACQUISITION  PARAMATERS,  APPLICATION SOFTWARE  AND  IMAGING  TECHNIQUES "]
["I.1","Techniques or softwares to reduce motion artefacts for peadiatric patients must be included in the system. Details of the availaible and offered softwares must be stated. ",1]
["I.2","Display slice, slab thickness,left and right designation:"]
["I.2.1","2D.",1]
["I.2.2","3D.",1]
["I.3","Variable field of view required to minimum of 48cm or better. State details.",1]
["I.4","Standard/Conventional and fast imaging techniques/ Sequences required for all the following applications with dedicated post processing:"]
["I.4.1","Neurology:"]
["I.4.1.1","Brain.",2]
["I.4.1.2","Conventional imaging sequences.",2]
["I.4.1.3","Spectroscopy (Single voxel and multi voxel). State if compatible with parallel imaging 2D / 3D.",2]
["I.4.1.4","Diffusion weighted.",2]
["I.4.1.5","Perfusion weighted. State sequences used.",2]
["I.4.1.6","Fast MRI sequences. State sequences used.",2]
["I.4.1.7","Tractography  / Fibre tracking .",2]
["I.4.1.8","Spine.",2]
["I.4.2","Cardiac:"]
["I.4.2.1","Functional evaluation.",2]
["I.4.2.2","Morphology.",2]
["I.4.2.3","Valvular analysis.",2]
["I.4.2.4","Coronary artery imaging.",2]
["I.4.2.5","Viability studies.",2]
["I.4.2.6","ECG gating.",2]
["I.4.2.7","Myocardial tagging.",2]
["I.4.3","Abdomen:"]
["I.5.3.1","Conventional sequences.",2]
["I.5.3.2","Virtual endoscopy.",2]
["I.5.3.3","MRCP.",2]
["I.5.3.4","Small bowel studies.",2]
["I.5.3.5","Dynamic liver contrast studies & Liver DWI.",2]
["I.4.4","Chest:"]
["I.4.4.1","Conventional sequences.",2]
["I.4.4.2","Mammography .",2]
["I.4.4.3","Dynamic (3D FSGRE).",2]
["I.4.4.4","Pulmonary ventilation studies.",2]
["I.4.5","Pelvis:"]
["I.4.5.1","Conventional sequences.",2]
["I.4.5.2","Prostate imaging (including spectroscopy).",2]
["I.4.5.3","Dynamic pelvic floor imaging.",2]
["I.4.6","Vascular:"]
["I.4.6.1","TOF (2D/3D).",2]
["I.4.6.2","PC (2D/3D).",2]
["I.4.6.3","Contrast enhancement for:",2]
["I.4.6.4","Neck vessel studies.",2]
["I.4.6.5","Intracranial vessel studies.",2]
["I.4.6.6","Aortic arch and branches.",2]
["I.4.6.7","Abdominal aorta and outflow.",2]
["I.4.6.8","Upper  & Lower limbs.",2]
["I.4.6.9","Pulmonary arteries.",2]
["I.4.6.10","Renal arteries.",2]
["I.4.6.11","Multistep MR angiography.",2]
["I.4.7","Head and neck:"]
["I.4.7.1","Conventional sequences.",2]
["I.4.7.2","IAM's (Internal Auditory Meatus).",2]
["I.4.7.3","TMJ's.",2]
["J","SAFETY"]
["J.1","Real-time SAR calculation shall be performed by software to ensure that RF power   levels comply with regulatory guidelines and be displayed on each image.",2]
["J.2","Pinpoint walk-through metal detector must be provided.Dedicated Ferro-magnetic detector with a pre-warning on approach well outside MRI room, not a conventional metal detector.  Highest sensitivity rating for the MRI environment.",2]
["J.3","Hand held metal detector with different setting sensitivity must be provided Highest sensitivity rating for the MRI environment.",1]
["J.4","Give details of comprehensive magnet safety and MRI safety /include details of isolation transformer,earthing details,anti-theft cables and stability of power supply requirements.",1]
["J.5","Air-conditioning: Water chiller with filter connected to UPS must be provided.",2]
["J.6","Three airconditioners should be supplied. Details of the airconditioners should be stated:"]
["J.6.1","18000BTU for the control room",2]
["J.6.2","32000BTU for the UPS",2]
["J.6.3","32000BTU for the MRI room",2]
["J.6.4","Online UPS 160kVA or higher",2]
["K","ADDITIONAL  EQUIPMENT"]
["K.1","Two MRI compatable patient vital signs monitoring screen at the console must be provided for adults and paediatrics.",2]
["L"," STANDARD ACCESSORIES "]
["L.1","MRI compatible headphones ",2]
["L.2","MRI compatible contrast injector interphased with MR unit. ",2]
["L.3","Drug Infusion pump compatible to MRI.",1]
["L.4","Patient Monitoring Video Camera System. Direct connection to monitor. All parts in the MRI room must be MRI compatible",2]
["L.5","Digital Patient weighing scale with maximum capacity of 200kg ",1]
["L.6","Patient slide for patient transfer (PVC Body Transfer Board and Storage Brackets)",1]
["L.7","MRI compatible wheelchair with footrests",1]
["L.8","MRI compatible laryngoscopes, a fully equipped MRI compatible emergency trolley and MRI compatible Stethoscope.",1]
["L.9","MRI Heavy Duty / Extra Wide Folding Walker.",1]
["L.10","MRI compatible steps / MRI Double Step Stool with Handrail",1]
["L.11","Drip Stand must be MRI compatible",2]
["L.12","4 operator ergonomic chairs on five-star frame with high back swivel with arm rests with load capacity of 200kg. ",1]
["L.13"," Remote service support.",1]
["M","MRI COMPATIBLE ANAESTHETIC UNIT "]
["M.1","MRI compatible anaesthetic machine with ECG, NIBP, SPO2 & Gas  capnography   to suit adults, pediatric and neonates. ECG: Echo Cardiogram / NIBP: Non invasive BP  / SPO2: Oxygen saturation /   Gas Capnography: CO2 measurement",2]
["M.2","Anaesthesia machine must have a scavenger and the room must have an outlet for the scavenger for anaesthetic gases to be removed from the magnet room.",2]
["N","OPTIONAL ITEMS (The following items must be quoted separately)"]
["N.1","State solution for Breast MR with optional interventional capabilities.Quote interventional capabilities as optional.",1]
["Total Score",null,{"$f":"SUM(C10:C187)","v":225}]
["Minimum Threshold",null,"180"]

{"sheet":"9. MRI 3T","index":9,"n_rows":189,"n_cols":7,"rows_kept":189,"merged":[[0,0,0,6],[1,0,1,6],[2,0,3,6],[6,0,6,6],[8,1,8,4],[22,1,22,4],[26,1,26,4],[39,1,39,4],[52,1,52,4],[66,1,66,4],[84,1,84,4],[86,1,86,4],[100,1,100,4],[155,1,155,4],[166,1,166,4],[168,1,168,4],[187,0,187,1],[188,0,188,1]]}
["ANNEXURE A: TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 180 out of 225 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item no. 9","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["MRI 3 T"]
["A"," Modality Details"]
["A.1","MAGNET"]
["A.1.1","The Magnet Field Strength shall be at least 3 Tesla active shielded.",2]
["A.1.2","The Magnet must be closed bore cylindrical type and design.",2]
["A.1.3","Bore length including all covers must  be a minimum of 140cm and not exceed 210cm.",1]
["A.1.4","The internal bore size must not be less than 70cm inner magnet. State the dimensions (L x W x H). ",1]
["A.1.5","Magnet homogeneity should meet the following specifications using the standard deviation VRMS (volume root-meansquare) using 24 plane plot measurement method. Provide the actual values of the magnet homogeneity. "]
["A.1.5.1","45 cm DSV (Diameter Spherical Volume) state (0.9 - 1.2 ppm)",1]
["A.1.5.2","40 cm DSV state (0.34 - 0.45 ppm)",1]
["A.1.5.3","30 cm DSV state (0.05 - 0.08 ppm)",1]
["A.1.5.4","20 cm DSV state (0.009 - 0.022 ppm)",1]
["A.1.5.5","10 cm DSV  state (0.001 - 0.0022 ppm)",1]
["A.1.5.6","Magnetic field stability shall be less than 0.1 ppm/hour.",1]
["A.1.5.7","The 5 Gauss/0.5mT fringe field must be contained in an area of radial and axial of 4-6m.  State actual area.",1]
["A.1.5.8","The minimum helium boil off rate should be less than 0.02 ltr/hr under normal operating conditions",1]
["B","MAGNET SAFETY"]
["B.1","Magnet must be equipped with quench exhaust leading to the outside of the building in event of Magnet quench to prevent injury to staff and patient/depending on type of cooling system available. State technology, vent pipe requirements (where applicable). ",2]
["B.2","Magnet must be equipped with emergency ramp down unit for fast Magnetic reduction and ramp up procedure, state details.",2]
["B.3","MRI Signage/Floor Sticker Warning Signs/MRI Symbols Sign/ MRI Zone Signs, “Do Not Enter” Floor Cones must be provided (Complete set).",2]
["C","GRADIENT SYSTEM (Provide advanced or latest technology details)"]
["C.1","Actively shielded hi-performance non-resonant gradient coil system must be supplied.",2]
["C.2","Gradient amplitude/peak strength must be at least 33mT/m measured per real axis plateau (100% duty cycle) not effective gradients: Sate options of highest gradients/Higher gradients will be an advantage.",1]
["C.3","Gradient duty cycle must be 100%.",1]
["C.4","Gradient rise time from 0 to maximum gradient amplitude must be 200 micro-seconds or more.",1]
["C.5","Gradient slew rate must be 120 m/mT/ms or more measured per real axis plateau, not effective values. Provide the data sheet/brochure of the slew rates parameters.",1]
["C.6","Scan matrix must be minimum of 1024 x 1024 or better. Maximum recon matrix must be stated.",1]
["C.7","The reconstruction speed at 100% FOV must not be less than 60 000 reconstructions /sec.",1]
["C.8","Gradient upgrades to different levels should be possible without changing gradient coil. State the details of the available upgrade for the gradient.",1]
["C.9","The system must have the gradient coil cooling system. Provide the details of the cooling system offered.  ",1]
["C.10","The output linearity of the gradient amplifiers should be maximum of  0.1% of peak.",1]
["C.11","The unit must have acoustic noise reduction mechanisms/system for all patients (adults & paediatrics).   ",1]
["C.12","Free choice of flip angle while maintaining signal to noise ratio to be supported. ",1]
["D","RADIOFREQUENCY SYSTEM"]
["D.1","Resonance frequency must be 128MHz or 3 Tesla. ",1]
["D.2","Direct Radio Frequency (RF) Transmitter System: Digital signal generation and processing must be possible. ",1]
["D.3","The transmission system must be integrated in the magnet housing.",1]
["D.4","Power output of transmitter amplifier rating must be 18kW or better.",1]
["D.5","The system must be equipped with RF fault protection limiting RF output in event of malfunction.",1]
["D.6","The receiver components must be integrated into the magnet housing.",1]
["D.6.1","Phased array acquisition system with minimum of 16 independent digital RF receiver channels or more must be supplied. State commercial available channel upgrade path and commercial available coils utilizing the number of channels. ",1]
["D.6.2","The system should have at least 32 independent RF receiver channels or better. ",1]
["D.6.3","Phase resolution shall be 0.1 degree/bit or better",1]
["D.6.4","Noise of the preamplifier to be less or equal to 0.5 decibels",1]
["D.7","The Digital receiver and transmitter amplitude must be 16 bit control or more.",1]
["D.8","All coil elements must be used seamlessly  in one study without coil changes and without repositioning of the patient. State maximum number of simultaneously connected coil elements.",1]
["E","RF COILS"]
["E.1","The bidder must supply market related Integrated Coil Technology. State how the Coil technology of the unit contributes and improve the Image Quality and Workflow. ",1]
["E.2","Integrated circular polarised/quadrature transmit and receive body coil.",1]
["E.3","It must be possible to select active coil or elements from the main console.",1]
["E.4","Standard coils for the following applications should be available with  the system:"]
["E.4.1","Body (Chest, abdomen, pelvis).",1]
["E.4.2","Head ",1]
["E.4.3","Whole spine.",1]
["E.4.4","Extremities and joints: wrist, hips, shoulder,  knee,  foot/ankle,",1]
["E.4.5","Breast MR. ",1]
["E.4.6","Whole body vascular and Peripheral vascular array.",1]
["E.4.7","Dedicated pediatric coils.",1]
["E.4.8","Supply an MRI compatable cabinet in the room for storage of all coils and other accessories.",2]
["E.4.9","Coils to facilitate optimal facial, calvarial and intracranial imaging in the child from 1.5-60kgs, including visualisation of the orbits, optic nerves, optic tracts, pituitary fossa, hypothalamus, temporal lobe, posterior fossa and cerebral cortex. Coils to provide optimal imaging including, but not limited to the clinical settings.",1]
["F","PATIENT SUPPORT/TABLE and MANAGEMENT/ PATIENT COMFORT"]
["F.1","Two dockable tables or a trolley with a fixed table must be provided and included in the total price",2]
["F.2","Dual table control panels shall be located at either side of aperture/gantry for easy access. State if controls are available on the rear of the magnet.",2]
["F.3","Centering  laser light beams for anatomical references.",1]
["F.4","Table movement shall be controlled from both gantry and operator console.",2]
["F.5","Patient table shall be equipped with manual override for quick removal of patient from the magnet-bore in case of emergency.",2]
["F.6","Maximum load must be  minimum of 140kg or better. State actual maximum load.",1]
["F.7","The following table movement functions must be possible:"]
["F.7.1","Accuracy of repositioning to last scan position.",1]
["F.8","Physiologic measurement unit essential with display of ECG, respiration and pulse at the main console and gantry.",2]
["F.9","Two way in-bore intercom system shall allow communication with patient while gradient is running.",2]
["F.10","Hand held alarm button for patient signalling.",2]
["F.11","Table restraining/immobilization straps are required per table.",2]
["F.12","Integrated music for patient shall be included.",1]
["F.13","Variable patient comfort lighting/ambience to be included.",1]
["F.14","MRI compatible sand bags and sponges in various sizes and shapes.",2]
["F.15","Ventilation in the gantry /Fresh air supply.",2]
["F.16","Auto-voice system.",1]
["G"," WORKSTATION: DOCTORS CONSOLE"]
["G.1","Two doctors workstations with a minimum 3 MP 19 inch or better reporting monitor  with touch screen must be linked to the main system and have their own independent consoles, allowing viewing, post processing and archiving.  ",2]
["H","OPERATOR USER INTERFACE"]
["H.1","Two 19 inch with touch screen or larger hi-resolution colour LCD flat-panel flicker-free monitor with undistorted image display required or better.",1]
["H.2","Resolution of the monitor must be 1024 x 1024 pixel or better",1]
["H.3","User interface providing flexible multi-tasking in foreground or background (scanning, filming, reconstruction).",2]
["H.4","6 TB external hard drive as storage devices required.",1]
["H.5","All standard image processing features are required in addition to the following advanced features must be available:"]
["H.5.1","Multi-planner reformatting (MPR).",1]
["H.5.2","Multi-projection volume rendering (MPVR).",1]
["H.5.3","Maximum intensity projection (MIP).",1]
["H.5.4","MR Angiography processing.",1]
["H.5.5","3D surface rendering.",1]
["H.5.6","MR Hydrography MRCP/Urography/Myelography.",1]
["H.5.7","Image add/subtract.",1]
["H.5.8","CT image display and intergration",1]
["I","ACQUISITION  PARAMATERS,  APPLICATION SOFTWARE  AND  IMAGING  TECHNIQUES "]
["I.1","Techniques or softwares to reduce motion artefacts for peadiatric patients must be included in the system. Details of the availaible and offered softwares must be stated. ",1]
["I.2","Display slice, slab thickness, left and right designation:"]
["I.2.1","2D.",1]
["I.2.2","3D.",1]
["I.3","Variable field of view required to minimum of 48cm or better. State details.",1]
["I.4","Standard/Conventional and fast imaging techniques/ Sequences required for all the following applications with dedicated post processing:"]
["I.4.1","Neurology:"]
["I.4.1.1","Brain.",2]
["I.4.1.2","Conventional imaging sequences.",2]
["I.4.1.3","Spectroscopy (Single voxel and multi voxel). State if compatible with parallel imaging 2D / 3D.",2]
["I.4.1.4","Diffusion weighted.",2]
["I.4.1.5","Perfusion weighted. State sequences used.",2]
["I.4.1.6","Fast MRI sequences. State sequences used.",2]
["I.4.1.7","Tractography  / Fibre tracking .",2]
["I.4.1.8","Spine.",2]
["I.4.2","Cardiac:"]
["I.4.2.1","Functional evaluation.",2]
["I.4.2.2","Morphology.",2]
["I.4.2.3","Valvular analysis.",2]
["I.4.2.4","Coronary artery imaging.",2]
["I.4.2.5","Viability studies.",2]
["I.4.2.6","ECG gating.",2]
["I.4.2.7","Myocardial tagging.",2]
["I.4.3","Abdomen:"]
["I.4.3.1","Conventional sequences.",2]
["I.4.3.2","Virtual endoscopy.",2]
["I.4.3.3","MRCP.",2]
["I.4.3.4","Small bowel studies.",2]
["I.4.3.5","Dynamic liver contrast studies & Liver DWI.",2]
["I.4.4","Chest:"]
["I.4.4.1","Conventional sequences.",2]
["I.4.4.2","Mammography .",2]
["I.4.4.3","Dynamic (3D FSGRE).",2]
["I.4.4.4","Pulmonary ventilation studies.",2]
["I.4.5","Pelvis:"]
["I.4.5.1","Conventional sequences.",2]
["I.4.5.2","Prostate imaging (including spectroscopy).",2]
["I.4.5.3","Dynamic pelvic floor imaging.",2]
["I.4.6","Vascular:"]
["I.4.6.1","TOF (2D/3D).",2]
["I.4.6.2","PC (2D/3D).",2]
["I.4.6.3","Contrast enhancement for:",2]
["I.4.6.4","Neck vessel studies.",2]
["I.4.6.5","Intracranial vessel studies.",2]
["I.4.6.6","Aortic arch and branches.",2]
["I.4.6.7","Abdominal aorta and outflow.",2]
["I.4.6.8","Upper  & Lower limbs.",2]
["I.4.6.9","Pulmonary arteries.",2]
["I.4.6.10","Renal arteries.",2]
["I.4.6.11","Multistep MR angiography.",2]
["I.4.7","Head and neck:"]
["I.4.7.1","Conventional sequences.",2]
["I.4.7.2","IAM's (Internal Auditory Meatus).",2]
["I.4.7.3","TMJ's.",2]
["J","SAFETY"]
["J.1","Real-time SAR calculation shall be performed by software to ensure that RF power   levels comply with regulatory guidelines and be displayed on each image.",2]
["J.2","Pinpoint walk-through metal detector must be provided.Dedicated Ferro-magnetic detector with a pre-warning on approach well outside MRI room, not a conventional metal detector.  Highest sensitivity rating for the MRI environment.",2]
["J.3","Hand held metal detector with different setting sensitivity must be provided Highest sensitivity rating for the MRI environment.",1]
["J.4","Give details of comprehensive magnet safety and MRI safety /include details of isolation transformer,earthing details,anti-theft cables and stability of power supply requirements.",1]
["J.5","Air-conditioning: Water chiller with filter connected to UPS must be provided.",2]
["J.6","Three airconditioners should be supplied. Details of the airconditioners should be stated:"]
["J.6.1","18000BTU for the control room",2]
["J.6.2","32000BTU for the UPS",2]
["J.6.3","32000BTU for the MRI room",2]
["J.6.4","Online UPS 160kVA or higher",2]
["K","ADDITIONAL  EQUIPMENT"]
["K.1","Two MRI compatable patient vital signs monitoring screen at the console must be provided for adults and paediatrics.",2]
["L"," STANDARD ACCESSORIES "]
["L.1","MRI compatible headphones ",2]
["L.2","MRI compatible contrast injector interphased with MR unit. ",2]
["L.3","Drug Infusion pump compatible to MRI.",1]
["L.4","Patient Monitoring Video Camera System. Direct connection to monitor. All parts in the MRI room must be MRI compatible",2]
["L.5","Digital Patient weighing scale with maximum capacity of 200kg ",1]
["L.6","Patient slide for patient transfer (PVC Body Transfer Board and Storage Brackets)",1]
["L.7","MRI compatible wheelchair with footrests",1]
["L.8","MRI compatible laryngoscopes, a fully equipped MRI compatible emergency trolley and MRI compatible Stethoscope.",1]
["L.9","MRI Heavy Duty / Extra Wide Folding Walker.",1]
["L.10","MRI compatible steps / MRI Double Step Stool with Handrail",1]
["L.11","Drip Stand must be MRI compatible",2]
["L.12","4 operator ergonomic chairs on five-star frame with high back swivel with arm rests with load capacity of 200kg. ",1]
["L.13"," Remote service support.",1]
["M","MRI COMPATIBLE ANAESTHETIC UNIT "]
["M.1","MRI compatible anaesthetic machine with ECG, NIBP, SPO2 & Gas  capnography   to suit adults, pediatric and neonates. ECG: Echo Cardiogram / NIBP: Non invasive BP  / SPO2: Oxygen saturation /   Gas Capnography: CO2 measurement",2]
["M.2","Anaesthesia machine must have a scavenger and the room must have an outlet for the scavenger for anaesthetic gases to be removed from the magnet room",2]
["N","OPTIONAL ITEMS (The following items must be quoted separately)"]
["N.1","State solution for Breast MR with optional interventional capabilities.Quote interventional capabilities as optional.",1]
["Total Score",null,{"$f":"SUM(C10:C187)","v":225}]
["Minimum Threshold",null,180]

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["                                                              TENDER SPECIFICATION"]
["TENDER SPECIFICATION FOR GT/GDH/020/2026:THE SUPPLY, DELIVERY, INSTALLATION, COMMISSIONING AND MAINTENANCE OF GENERAL AND SPECIALISED RADIOGRAPHY IMAGING EQUIPMENT AT VARIOUS GAUTENG HEALTH INSTITUTIONS FOR A PERIOD OF THREE YEARS"]
["Note:                                                                                                                                                                                                                                                                                                                                                                                                                                              \na. The Product Specification listed below must be completed and submitted in its original format\nb. Bidders will score a weighting of ‘2’ or ‘1’ depending on the weighting requirement per line item. Where a bid is non-compliant with the specification/s of that line item the bid will be scored ‘0’. \nc. The scoring of the bids:\n    i.Each specification will have a weight of 1, or a 2, which indicates the level of importance, as follows: \n      • A specification (line item) with a weight of 2 is a specification with a very high level of impotency that should be complied with.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                \n      • A specification (line item) with a 1 weight is a specification with a standard level of importance.\nd. Bidders are required to indicate compliance/non-compliance with the specification by typing 'YES/NO/Not applicable' on each line item column D.\ne. In the case where a bidder indicated ‘No/Not Applicable’ and an equivalent or better option is provided, bidders must type ‘Yes’ on relevant column E. Details of the equivalent/better option must be provided on column F. Bidders must note that where an equivalent or better option is provided, an equivalent weighting will be allocated as per the scoring on the line item.\nf. Bidders to provide reference to brochure (page number) / technical data sheet / Any supporting documents as evidence.\ng. Bidders must score a minimum threshold score of 50 out of 62 of the total points to qualify for the next stage of evaluation.                                                                                                                                                                                                                                                                                                                                                                                                                           "]
[]
["A","B","C","D","E","F","G"]
["Item no 10","Tender Specification","Weigting","Complyng with specifications (YES/NO/Not applicable)","Where Applicable Provided Equivalent/Better          (YES/NO)","Provide details of Equivalent/better Product Offer in this column                                           (You are advised to be straight to the point)","Bidder to indicate the exact page number where the specification can be found in the Brochure / Technical Data Sheet /  Any Supporting Document"]
["One Shot Scoliosis Imaging"]
["A","General"]
["A.1","Two portable and wireless, high capacity, direct digital flat panel, battery-powered detectors with a portable operator's console for each must be  provided: Active imaging size must be: \na. 24cm x 30cm                                                                                                                                                                                                                                                                                                                                                                                      b.43cm x 43cm. \nThe effective/active sizes and dimensions must be stated for both detector sizes. Bidders to offer an option of buying the detectors separately.",2]
["A.2","A wall mounted detector cabinet for the storage of wireless detectors must be included in the offer",1]
["A.3","The offered detectors must be configured to actively and optimally function with any general X-Ray rooms at no additional cost to the end-user. Provide the details of the interconnection configurations.",2]
["B ","Wireless Flat Panel Detectors"]
["B.1","The equipment offered must have a high shock tolerance and water resistant. Provide the details of the safety and protective features for each detector. ",2]
["B.2","The equipment must be offered with a radiolucent shock resistant protective cover. Provide the details of the material and durability of the covers. ",2]
["B.3","The offer must include two light weight, shock resistant, hardbody carry cases with sponges and wheels to protect the equipment during transport to the wards. Each carry case must fit one detector and console as well as an additional battery. The bidder must give an option of buying this item separately as and when required.",1]
["B.4","Image transfer must be done as follows (to the console): "]
["B.4.1","Wireless communication (WI-FI) & LAN must be enabled. State other available latest modes of image transfer.",2]
["B.4.2","Systems must have both 2.4GHz and 5GHz wireless transmission.",1]
["B.5","A. 43cm x 43cm flat panel detector: "]
["B.5.1","The scintillator must be Amorphous silicon photodiode.",2]
["B.5.2","The battery provided must be lithium or better. ",1]
["B.5.3","Pixel size/pitch must be 140 micrometer (µm) or smaller. ",1]
["B.5.4","The acquisition and digital conversion of the image from the flat panel of 14-bit or more. Details must be stated in the supporting documents provided . ",1]
["B.5.5","The image resolution must be at least 3.5 line pairs/mm. Details are stated in the supporting documents provided. ",1]
["B.5.6","The sytem must accept a minimum of 40kVp - 150 kVp.",1]
["B.5.7","The preview display time must  be 5 seconds or less. Details are stated in the supporting documents provided. ",2]
["B.5.8","The full image cycle time should be a maximum of 10 seconds.Details are stated in the supporting documents provided . ",2]
["B.5.9","The detector must be able to store a minimum of 100 images in the internal memory. The internal panel image storage capacity must be stated in the supporting documents.",1]
["B.5.10","The uniform load that the detector must be able to withstand should be at least 150kg. Details are stated in the supporting documents provided . ",1]
["B.5.11","The local load (on an area of 40 mm diameter)  that the detector must be able to withstand should be at least 100kg. Details are stated in the supporting documents provided .",1]
["B.6","24cm x 30cm flat panel detector: "]
["B.6.1","The scintillator must be Amorphous silicon photodiode.",2]
["B.6.2","The battery provided must be lithium or better. ",1]
["B.6.3","Pixel size/pitch must be 140 micrometer (µm) or smaller. ",1]
["B.6.4","The acquisition and digital conversion of the image from the flat panel of 14-bit or more. Details must be stated in the supporting documents provided . ",1]
["B.6.5","The image resolution must be at least 3.5 line pairs/mm. Details are stated in the supporting documents provided. ",1]
["B.6.6","The sytem must accept a minimum of 40kVp - 150 kVp.",1]
["B.6.7","The preview display time must  be 3 seconds or less. Details are stated in the supporting documents provided. ",2]
["B.6.8","The full image cycle time should be a maximum of 6 seconds.Details are stated in the supporting documents provided . ",2]
["B.6.9","The detector must be able to store a minimum of 100 images in the internal memory. The internal panel image storage capacity must be stated in the supporting documents.",1]
["C","Battery"]
["C.1","The following battery charger must be included for each detector:"]
["C.1.1","Four rechargeable batteries, two per detector must be provided. The battery should be able to handle 5 hours of active use when fully charged. Provide details of battery activity durations. ",2]
["C.1.2","Multi-slot charger to be provided. ",2]
["C.1.3","Charging time for each battery from fully depleted to fully charged should be less than 6 hours.",1]
["C.1.4","The rated power input must be: 220 - 240V AC, 50Hz, single phase.",2]
["D","Grid "]
["D.1","An encasement with a built in grid that fits the 24cm x 30cm or 43cm x 43cm detector must be supplied.  ",1]
["D.2","The grid must have at least:"]
["D.2.1","Grid ratio 8:1",1]
["D.2.2","Must be usable with FFD of 100cm to 180cm ",1]
["E","Operator's Console - Acquisition and Image Processing View Station"]
["E.1","The operator's console must be portable laptop with the latest operating software (iCore 7 or better).",2]
["E.2","A protective casing/bag for the operator's console must be included.",1]
["E.3","The operator's console must connect wirelessly to PACS/RIS/Printer.",1]
["E.4","The operator's consoles must be touch screens for user interface. Type of screen and user interface is stipulated in the supporting documents provided.",2]
["E.5","Print option to a DICOM DRY LASER printer must be possible.",2]
["E.6","The DICOM Modality Work list must be displayed on the screen and form part of the workflow.The worklist must allow for the display of examinations scheduled and performed and must reflect the date, time and patient details of each examination. It must also be available as a global network query. Details are stated in the supporting documents provided . ",1]
["E.7","The equipment must connect to RIS and PACS wirelessly and must be able to receive patient demographics from the RIS. ",1]
["E.8","It must be possible to enter all patient data and demographics manually in the event that the RIS is unavailable.",1]
["E.9","Image post-processing tools must be included. Details of post-processing tools must be stated.                                                                                                                                                                                                                                                                                           ",1]
["E.10","Exposure factors must be displayed on the screen. Details are stated in supporting documents provided .",1]
["TOTAL ",null,62]
["MINIMUM THRESHOLD ",null,50]