Technical Particulars For MEDIUM END 3D COLOR DOPPLER ULTRASOUND MACHINE.. For RC Period ( To )

Transcription

1 Technical Particulars For MEDIUM END 3D COLOR DOPPLER ULTRASOUND MACHINE.. For RC Period ( To ) Generated on: December 22, :46 PM NIC Schedule Unit : 1 NOS. Medium End 3D Color Doppler Ultrasound Machine Description LCD monitor size >= in cm (in inch) 1 2 Supply of Medium End 3D Color Doppler Ultrasound M 43 (17) achine as per GTS Supply of Medium End 3D Color Doppler Ultrasound M 48 (19) achine as per GTS Schedule Unit : 2 NOS. CMC charges [MECD] for Item No.1 of Schedule No. 1 Description CMC Charges for first year after warranty CMC Charges for second year after warranty CMC Charges for third year after warranty CMC Charges for fourth year after warranty CMC Charges for fifth year after warranty Schedule Unit : 3 NOS. CMC charges [MECD] for Item No.2 of Schedule No. 1 Description Page 1 of 9

2 CMC Charges for first year after warranty CMC Charges for second year after warranty CMC Charges for third year after warranty CMC Charges for fourth year after warranty CMC Charges for fifth year after warranty Page 2 of 9

3 Detailed Specification Schedule 1 Medium End 3D Color Doppler Ultrasound Machine Specification : As per GTS Schedule 2 CMC charges [MECD] for Item No.1 of Schedule No. 1 Specification : Annual CMC Charges for Item No.1 of Sch No. 1 Schedule 3 Specification : CMC charges [MECD] for Item No.2 of Schedule No. 1 Annual CMC charges for item no. 2 of Sch. No.1 Page 3 of 9

4 General Technical requirement For TE : ================================================================== General Technical Specification (GTS) for Medium End 3D Color Doppler Ultrasound Machine ================================================================= Technical Specification: The equipment must be capable of operating in B, M, Doppler, Color flow and Power Doppler modes. It must support transducers with linear, sector and convex formats. Further, it must include a full array of measurement and calculation packages. The specific minimum requirements for this equipment are as follow. 1. User Interface & Ergonomics 1.1. The system shall include at least a 43 cm (17 inch) / 48 cm (19 inch) (as specified under different schedules) LCD inbuilt monitor with 1280 x 1024 resolution to allow for both excellent image viewing as well as providing for workflow and productivity features The monitor shall tilt +20 degree/-90 degree and rotate +/- 90 degree independent of console to provide maximum usability The LCD monitor shall be mounted on an articulating arm that moves side-to-side, forward and backward The system shall have at least three active probe ports in a convenient, easy to access location to maximize the availability of needed probes System shall have image management features that store images by patient and include the ability to review images from different exam dates System shall support the ability to store digital raw data that allows optimizing imaging parameters such as B Gain Color Gain, Gain, Doppler Base Line on real time images or images recalled from image archive or frozen images System shall allow for live image and archive images side-by-side on a single monitor. This display shall allow any type of image- B-Mode, Color, or power Doppler on either side The system shall display thumbnails on a clipboard while scanning to facilitate exams The dynamic range should be more than 180 db Frame rate should be 700 fps or more. 2. Workflow 2.1 The system shall have build in protocols for applications such as abdominal, vascular and urology and OB/GYN, and should also allow flexibility so that operator or department specific protocols can be set up. 2.2 In particular automation should include * Automatic insertion of comments * Automatic set up of imaging controls and modes * Automatic steering in Color and Pulsed Wave Doppler * Initiation auto-completion of required measurements Page 4 of 9

5 * Intuitive advancement to the next step in an exam * Automatic preset selection by transducer, user and exam type * Automatic Program selection 2.3 The system shall incorporate enough flexibility so that the program can easily be paused and resumed. 3. Raw Data Processing. 3.1 The system shall allow for image manipulation on real time or frozen images to provide maximum image flexibility, review and productivity. It shall include, at a minimum the ability to change the: * Overall B-Mode gain, Overall Doppler gain, base line shift, sweep speed and inverted spectral waveform. * Anatomical M-Mode 3.2 The system shall provide a display zoom function on frozen images. 4. Scanning Parameters 4.1 The system should have at least 50,000 digital processing channels 4.2 The system shall possess the ability to control speckle through the use of a speckle reduction algorithm that enhances borders, reduces speckle artifact and improves detail and contract resolution 4.3 The system shall provide the ability to scan in the compound imaging mode with up to 9 lines on all vaginal and convex probes. (multiple steps) 4.4 The system shall provide scan depths from a minimum of 2 cm to a maximum of at least 30 cm. 4.5 The system shall be capable of operating in the following modes: B-Mode, M-Mode, Doppler, Color flow (CF), and Power Doppler Imaging. The following mixed modes shall be available: * B/M, B/Doppler * B/CF * B/Power Doppler * B/Doppler/CF * B/Doppler/Power Doppler * B/CF/M-mode. * 3D Volume Imaging package to be provided(convex and TV probe) 5. B-Mode/ M-Mode Imaging 5.1 The system should have Tissue Harmonic imaging & should be available in Convex, Linear, Sector & Volume probes 5.2 The system shall provide user selectable levels of frame averaging or persistence for noise reduction. 5.3 The system shall provide user control over the displayed dynamic range. 5.4 The system shall provide selectable levels of edge enhancement. Page 5 of 9

6 5.5 The system shall provide the user with user-selectable gray scale maps and the ability to program and save user programmable maps. 5.6 The system shall have an "anatomical" M-Mode -allowing the M-Mode cursor to be adjustable in any plane and allow for accurate measurements. 6. Color flow/power Doppler 6.1 Color flow/power Doppler shall be available for all probes. 6.2 The system shall provide a user controlled mechanism to easily control the size and position of the color flow/power Doppler Region of Interest (ROI) including independent control of it's height and width. 6.3 The system shall support a large range of velocity scales that can be easily adjusted by the user. 6.4 The system shall provide the user with a frame rate/resolution control (line density) that varies the acoustic beam density. 6.5 The system shall provide a user selectable control to vary the color flow/power Doppler frequency. 6.6 The system shall provide a real-time triplex mode (B + PW/CFM/PW). 7. Spectral Doppler (PW) 7.1 Doppler mode shall be available on all probes. 7.2 The Doppler cursor shall be user-steerable with linear transducers. 7.3 The system shall provide the user with control to either have Doppler with real time B-Mode, Doppler with periodic B-Mode update or Doppler with frozen B-Mode scanning. 7.4 The system shall provide stereo audio of the Doppler spectral signal. 7.5 The system shall provide the user with control during timeline replay to review the spectrum only (i.e., frozen B-Mode) or with the spectrum and B-Mode together and synchronized. 7.6 The system shall provide the user with the ability to add a spectral peak and spectral mean trace onto the spectrum in both real time or after freezing the image. 8. Measurements and Calculations 8.1 Measurements should be possible on frozen images as well as on images recalled from the image archive. 8.2 The system shall provide a comprehensive set of obstetrical and gynaecologic calculations and vascular calculations with summary reports. 9. Image Archive and Networking 9.1. The device should store images onto an integrated DVD-R Multridrive and a USB port storage device. Page 6 of 9

7 9.2. The system shall include at least 500 GB of dedicated hard drive for large local storage capacity System should have Cine loop review facility in individual and mixed modes with memory up to minimum of 400 images and 30 seconds of Doppler M Mode data The system shall provide the ability to sort images stored on board based on either patient name or exam date The device should store images in DICOM, JPG, WMV and AVI formats for maximum flexibility. 10. DICOM Connectivity The system shall support as an option for DICOM service classes: The ability to retrieve DICOM Images from other Imaging Modalities than Ultrasound. 11. Transducers i. Convex, Operating Frequency: 1-5 MHz (+/- 1 MHz) ii. Trans-vaginal probe, Operating Frequency: 3-9 MHz (+/- 1 MHz) with FOV of 160 degrees or more iii. Linear Probe for Peripheral vascular Studies 5-12 MHz. iv. 3D Convex volume Transducer 12. System should provide HD Zoom. System should have Quick start presets/sub presets so that the presets can be adapted to the changed probes. 13. Accessories B/W thermal printer of latest model Biopsy attachment for the Convex, Linear & the endocavitary probes Voltage Stabilizer On line UPS with capacity for half an hour backup to support all functions of the equipment i.e. performing ultrasound procedure, exposure on to films or copy on a CD. Machine cover and transducer sheaths 100 gel bottles and 50 printing rolls 100 sterilized probe cover. Two sets of operating manuals 14. Warranty: Five (5) year comprehensive onsite warranty of for complete equipment (Including all spares & labour) and all other components of the system from the date of satisfactory Page 7 of 9

8 installation of the equipment. 95% up time 24x7x365 days Warranty of complete equipment with provision for extension of Warranty period by double the downtime period. All software updates should be provided free of cost during Comprehensive Warranty period. 15. CMC: Comprehensive Maintenance Contract (CMC) equipment for 24x7x365 days (including all spares and labour) covering of the complete equipment as well as accessories and auxiliary units supplied. CMC is also to include preventive maintenance including testing & calibration as per technical/ service /operational manual of the manufacturer, labour and spares, after satisfactory completion of Warranty period may be quoted for next 5 years on yearly basis for complete. 16. Product Datasheet: (i) The bidder should submit the product datasheet, brochure and compliance sheet, without which the bid will be rejected. Computer generated datasheet/brochure will not be accepted. Please mark the serial number of specification in the compliance sheet and datasheet. (ii) When required, information other than those in the data sheets would be provided as a separate document format by the Principal(s)/Original Equipment Manufacturer(s) only and should refer to the specific section(s) being addressed. When standard vendor data sheet disagrees with the bid response (Offer/ compliance statement), clarification should accompany in the form of a certificate from the principals/oems only. In absence of this, the vendor data sheet will prevail for the purpose of evaluation and decision of the technical committee shall be final and binding on the supplier. 17. Training: The vendor to provide adequate onsite application training to the end user for a period of two (2) weeks duration, within the period of 2 months of supply. 18. Approvals: The complete equipment should be CE(European) and US-FDA approved TP Prepared By TP Scrutenised By Name Gaurav Sharma Desig Director (MS) Date TP Recommended By Gaurav Sharma Director (MS) TP Approved By Name Gaurav Sharma Page 8 of 9

9 Desig Director (MS) Date DDG(QA) Forwarded to(purchase Dte.): Medical Stores With Ref. To(Pur. Wing No.): QA Wing Ref. No. Page 9 of 9