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Annexure-A Specification.xlsx

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2. nR 200 Nos event recall snapshot facility both manually and automatically triggered by alarm P103 Automatic zoom in facility in the monitor display e s a The monitors should have monitor to monitor overview facility and data transfer over the network T B Integrated or external printer for report output optional 3 SYSTEM CONFIGURATION ACCESSORIES SPARES AND CONSUMABLES 1 ECG Resp one module with a set of 5 Lead ECG cable with clip 2 per monitor NIBP One module per monitor Adult cuff 2 nos per monitor and two sizes of pediatric cuffs one per monitor neonatal reusable cuff two monitor complete sets SP02 One module per monitor Reusable master mother cable 2 nos per monitor Reusable Adult sensor finger clip type 2 nos Reusable Pediatric sensor clip sleeve wrap around type 1 no IBP One module per monitor with 2 Nos of reusable transducer cable and disposable transducers 20 Nos per monitor Temperature One module per monitor Rectal temperature probe 2 per monitor and skin temperature probe one per monitor EtCO2 Sidestream one module per six monitors with all accessories 10 sets of sampling tubes for each module to be included ardiac Output Continuous cardiac output module one per six monitors with accessories acility to mount the monitor on patient bed transport trolley N OWER SUPPLY ower input to be 220 240 V AC 50 Hz 5 STANDARDS SAFETY AND TRAINING PT S
3. 3 The system shall be able to be connected to an optional footswitch for hands free operation L vp e rn B w Thermal Printer of latest model with CE or FDA mark ee UPS of appropriate rating with 60 mins back up additional to in built battery back up 4 POWERSUPPLY 1 JPower input to be 220 240 V AC 50 Hz 5 STANDARDS SAFETY AND TRAINING PT Should be FDA CE BIS approved product o P2 Manufacturer should have ISO certification for quality standards ae On Site Comprehensive training for lab staff and support services till customer satisfaction with the system 6 DOCUMENTATION E d su ij User manuals to be supplied in English o ue a Service manuals to be supplied in English DepartmentSINo UU Equipments s OOOO BomedislAset No OOOO Qm y B o 7 7 Smir ems SL NO SPECIFICATION up m IPC E B a HehfequenymoblexraymachnewihmiimumouputofZSKW av range 40 KV to 100 KV with atleast 20 KVstes SSCS MeximumrmAoutput notlessthanGO mA wihatleast20stepsofmAormAs 2 rhe machine shouid have a double slot manual light beam collimator s oisptay Digital display of atleast maS and kV for easy parameter settings The X ray machine should be single tank light weight and easy to move around It should have a disinfectable control BERNER c0 77 ee UU BENE ei eed counterbalanced with rotation in all directions
4. 6 The machine should be equipped with double step exposure switch withlongcord PF TT It must have an articulated arm for maximum positioning flexibility in any patient position 8 tsheudalohavecassettestorageboxforallstesofcassettes S The unit should run on 1 phase 200 250 volts with voltage compensation 10 should be microprocessor controlled high frequency output 2 5 KWorabove E LN mE Should have the ISO certification and the copy of the same should be enclosed along with the technical bid EE quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid rwo numbers of complete User Technical Maintenance manuals tobe supplied in English Teertfcate of calibration and inspection fromfactory SOS DBermensiNo OOS RupmensNo e O OOOO BomedialAset No OOS Quy Bo Smarten OOOO SL NO SPECIFICATION 1 s een specien OO Technical specification A Generator S O Should be microprocessor controlled high frequency generator with 2 5 kW or more with integrated beam filters to reduce patient skin radiation gose 8 __eollimator shouldbe IRIS ormultieaf O O OOOO C X Ray mode kV amp mA range S O __ kv range shouldbe 0 110 OOOO O O O OSS D Fluroscopy S O __ ___Fluroscopy mA range shall be from 02 to6ma O
5. RupmemsNo pa O O OOOO LL BomedialAset No O OOS Quantity Bo Smarten SSS SL NO SPECIFICATION oa Description of Function Anesthesia Workstation is used for delivering anesthesia agents to the patients during surgery The complete unit also monitors the vital signs and ventilates the patients 2 Operational Requirements Anaesthesia machine complete and integrated with Anaesthesia gas delivery system Circle absorber system Precision vaporizer for isoflurane Sevoflurane and Desflurane optional Anaesthesia ventilator NN system to monitor Anaesthetic gases ECG EtCO2 FiO2 Online O2 Analyzer Pulse Oximeter and airway NN peak plateau and mean NIBP IBP rectal amp skin temperature dt Essential accessories to make the system complete and compatible with the existing system of gas outlets PF o a Demonstration of the equipment as per specifications is a must 3 Technical Specifications 1 Flow management Ooo ae Should be Compact ergonomic amp easy to use Doo P3 Machine should provide electronic gas mixing hn xb i Multi color TFT display of at least 12 size with virtual flow meters for O2 N20 or Air b xp erc Dual flow sensing capability at inhalation and exhalation ports Should have back up O2 control which provides an independent fresh gas source and flow meter Manual Control in case of electronic failure o 7 Gas regulators shall be of modular design g
6. 3 jubWermglfesBohrs O O OOOO 4 Digital Bulb life counter on light source S 3 jAwtema c MenwllightAdjustment OOOO SS 6 j sadByMede O 7 Universal Jaw Assembly to adapt any make of fiber optic cable wihoutadapter gcc Ua 4 Fiber optic Cable S 1 je5mm ZsfeetSnapFitcabe O EE ERN gia 5 Monitor S L cb We jj 19 Flat Panel Monitor Colour pecu PAR 6 mea 3 Jutrofhghfw LL 2 jWempocsorcmwokdust s Soft approach Pressure control for safe recovery of abdominal pressure Pa ease 5 ic based central display monitor with multilingual tet amp graphics O 6 jwwenmggul 0000000 pop Suction irrigationPump taparoscopes Fully Autoclavable with working length 300mm Wieaneddsteionfreeew OOOO iversal adaptor for other ight sources O Jreliow Glass index for optimum evenness of focus amp contrast o pamen OOOO o o Bodgesimm OOOO T pages LL Hewbevdeoteesope RECTA NET eee 7 Specifications T 1 Laparoscopic hand instruments reusable with 310mm working length take apart locking unlocking mechanism rotable with interchangeable handle with monopolar diathermy attachment Except veress needle 2 eresmedeizemlenghc
7. Should have X ray luscent back section made up of high pressure laminate ABS 4 Should have X ray cassette holder underneath the back section It should be possible to insert and take out the cassette from the holder from either side of the bed without disturbing the patient 5 Base frame and support frame should be fabricated using steel square rectangular section of adequate cross section and thickness to provide high structural strength and stability Lh 391 Should have the following ranges of movements nearest movements hydraulic gas spring actuated controlled 7 Height 480750 mm P8 Back section 0 50 degrees Leg section 0 30 degree Should have manual quick release button CPR release for back section to tackle emergency situation Actuation mechanism should be preferably gas spring actuated 11 Trendelenburg reverse Trendelenburg range should be 252 152 Should have four numbers of articulated half length tuck away side rails or two full length collapsible side rails 10 11 a engh 30O280 OOOO b jweisso igomm C L o Mattress size to suit the bed surface mattress times 12em a7 Jshould have detachable head end andfootend Mattress should be made up of high density foam with antimicrobial agent incorporated in all parts to assist 18 prevention of bacterial and fungal growth Cover should be of high quality washable durable and antimicrobial leather like synt
8. 7 wdevswlaamsfort OCS p tow supply pressure OOOO bs High tow airway pressure O OOOO SS je eweg Diometin OOOO O O a Powrf we 0 LL je Ame 0000 O owe E 1 a ivso iomL LL 8 pb PEPKPARRPS OOOO e RRuptod bm SSCS a hEmdoi2tozdd pe F022 100 LL o Should have battery back up for minimum 2 hours and additional port for recharging from ambulance io shoul fix on rails oftransport trolley and on standwithwheels CS 3i JPower input tobe 220 240VAG s0 O O OSS SSS 12 should have integrated display of minimum 6 inch diameter le Ue E 2 SYSTEM CONFIGURATION ACCESSORIES SPARES AND CONSUMABLES a Adutt reusable autoclavable silicon patient circuit 04 Nos Each ventilator 2 Jonygen Hose 01 Each ventiiator OOOO Air Hose 01 Each ventilator DINEM UNE NND Oooo o oa Rechargeable batteries 01 set Each ventilator 5 12Vcar charger 02 Nos in total E S Ee a EEE HME filters 200 Nos Each ventilator ea a STANDARDS SAFETY AND TRAINING NENNEN Should have the ISO certification and the copy of the same should be enclosed along with the technical bid 5 ode The quoted model should have CE BIS certificate and copy of the same should be enclosed along with the technical bid 4 DOCUMENTATION oo o es ee User
9. All panel key should be customized including Freeze Key 28 Color Map resolution up to 128 levels Facility for high definition digital acquisition review and editing for complete patient studies Should have facilities and application software for adult abdominal obs gyn peripheral vascular musculoskeletal 15 small parts imaging and endocavitary applications All application package should be built into the system Transcranial cardiac chest tissue doppler ME 2 2 2 24 2 2 4 Active Ports should be available 4 parking ports or more Any Probes any Port interchangeable connectivity should be possible with simple electronic selection method for interchanging transducers Detailed Radiology obs amp gyn and vascular measurement packages should be available System should have extensive calculation packages 32 a Distance volume Area stenosis on B mode b Distance Time Heart Rate Slope on M mode c Velocity Acceleration time Slope PI RI S D Ratio with Auto Doppler calculation on Doppler mode d Diastolic systolic and 2D Strain cardiac function packages The system should have Up Down amp Right Left Image rotation One touch Image optimization and Edge Enhancement settings HN uu HERUM Rs HN pret 30 Unit should have4transducersholdersandonegelbottleholder O Ea poe Hp un and PRF adjustment System should have automatic real time quantification of doppler
10. B Power Angio B and Power Angio should be available System shall have 3D imaging on all transducers System shall have curved and endovaginal 4D capabilities Non Doppler 2D Strain imaging 2D Tissue Doppler color coded EN 11 The system shall support full screen display of all 3D views including individual X Y and Z MPR views and ME Cine loop facility both frame by frame and in cine mode with a memory for atleast 2000 2D color images review and atleast 100 seconds of doppler and M mode data 37 ih frame rate review for better clarity of playback images study in slow motion 18 Quadloopwithmemoryforpreandpostimagecomparonofanyprocedure 19 Memory 2000 frames or more in quad loop M Mode amp Doppler scroll memory 40 seconds or more 20 rrame grabber facility forpostanalysis OOS S S Various maps for pre and post processing 1 2 System Dynamic Range should more than 160db 3 User defined system and application presets for multi user department The number of application presets is to be mentioned In built hard disk storage capacity of atleast 160 GB with facility of direct storage and retrieval of B W and color images both frozen and cine loops CD DVD drive for read and write of stored images 5 Depth of Field of 30 cm should be available 6 PRF Range should be 500 Hz to 50 000 Hz 27 Alpha numeric key board with illuminated keys and status display Key panel Height Adjustment Should be Possible
11. Lx On site comprehensive training for lab staff and support services till customer satisfaction with the system 5 Documentation S S hm 7 User manuals to be supplied in English o gps 2 Service manual to be supplied in english Department SI No EpmensNo a OOOO Biomedical Asset Nor OOOO quantity Bo Smarten SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS Should should be latest generation state of the art portable color Doppler for abdominal vascular musculoskeletal small parts basic cardiac and nerve block application with suitable evaluation and measurement packages 2 TECHNICAL SPECIFICATION li ca he ON System should be offered with following electronic multi frequency Broad Band width transducers FOR 6 DOPPLER UNITS Convex array transducer frequency range of 2 to 6 mHz for general purpose abdominal gynecological and obstetric imaging a a Linear array transducer 6 to 13 mHz for small parts breast vascular musculoskeletal nerve and superficial 2 imaging With biopsy facility nme phased array sector transducer 1 to5 mHz for cardiac imaging 4 Transcranial doppler probe OPTIONAL System should have following modes i 2 D M Mode Pulsed Wave Continuous Wave Color flow imaging amp color power angio ii Tissue harmonic imaging should be available in all transducers Digital Processing Channels 120 or more digital channels for high resolution imaging with acquisiti
12. Technical Specifications Light should comprise of 2 units one major diameter around 90 cm and one minor diameter around 55 cm Each unit should have a central light bulb Should have a facility of continuous brightness adjustment The light should be easily maneuverable and should have a swivel radius of at least 150 cms and height adjustment of at least 100 cms HN E E JE 8 mis i ia 1 Major unit should have 130000 lux and minor 100000 lux 5 The optimum colour temperature of the light should be between 4200 4700 kelvin with colour rendering index of atleast 90 22 ee es Each unit should provide a prefocussed beam of light with atleast 50 cmsdepth of field It should be a cool light and should not interfere with the laminar air flow system The absorption of infrared 7 radiation should be more than 99 and infrared radiation to feet at 100000 lux should be less than 35 w per sq metre Oo o d o O JE SEES pur Jp B The handle should be autoclavable amp detachable B 533 a System Configuration Accessories spares and consumables an er FEE 25spare bulbs should be included za i Standards Safety and Training Should have the ISO certification and the copy of the same should be enclosed along with the technical bid The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid Training should be provided for users and biomedical engineers Documentation s
13. 2 rempprbeRetaRewabeQg 13 AeesoresAnesthe cgssesO1set O O OCOS 34 accessories for Continuous Cardiac Output module O1set o o 15 accessories for neuromuscular transmission monitor 01st 16 Standara accessories to make all parameters working O1set O O 7 17 Disposable Adult amp Paediatriccircuts S0eah OO O OOOO 38 HM fiteeS0 OOOO LL 19 vital Parameter Accessoriesi Set OOS 20 should be supplied with negative pressure leak test equipment Eu IVO s mWommemalados fh owe The unit shall be capable of operating continuously in ambient temperature of 100C 400C and relative humidity of 1 I dm ee The unit shall be capable of being stored continuously in ambient Shall meet IEC 60601 1 2 2001 Or Equivalent BIS General Requirements of Safety for Electromagnetic 3 Compatibility Safe disposal system port of waste anesthetic gases AGSS Anesthetic Gas Scavenging System Port should be in place Supplier will be held responsible if this is not ensured at the time of installation Power Supply Power input to be 220 240VAC 50Hz 440 V 3 Phase as appropriate fitted with Indian plug Resettable over current breaker shall be fitted for protection Suitable Servo controlled Stabilizer CVT UPS of suitable rating shall be supplied for minimum 1 hour backup for the entire system 7 Standards Safety and Training pce
14. C O Pulsed fluoroscopy with last image Hold LIH S O E Rdegapy LL Radiographic mode for cassette exposures not less than 20mA oo O IIO 9 or more dual mode image intensifier with CCD camera O T 00000000000000000 LL I ia Minimum 12 bit digital flurosocpy imaginig unit with dedicated video pip line processor Digital image storage capacity for atleast 200 images and facility for CD DVD burning JCassette holder should be detachable for film recording Cassette size preferably 24x30cm A imageDispayOOCSC CSCSCs S Y Should have two 17 TFT LCD high resolution high contrast and flicker free monochrome monitors of at least 1024 x am 1024 matrix with automatic adaptation of monitor brightness to ambient light E cp eee System functionality i i C arm film focus distance should not be less than 90 cm and immersion depth not less than 70 cm Po Vertical Horizontal and orbital travel should be available and specified ae C ARM rotation should not be less than 120 degrees EN The system should be DICOM 3 0 compatible with connectivity to any network or computer in DICOM format Features like real time edge enhancement contrast and brightness adjustment video invert and dynamic movement detection to detect motion blurr should be available Foot switch for hands free and sterile control of Xray LUN a a a 2 Accessories o O ae l Wrap around li
15. OOOO O Jy Occlusion Pressure LL jg Spontaneous preathingtial C SCS SC SCSCSCSCSCSC CNNNNCNSN jg Faciityto calculate lower and upper inflection point O O o EGGS MR PAREN KM NK Reusable face mask with textured dual flap silicon cushion flap for easy fit Removable forehead support and pad to match the angle of patient s forehead stability selector for easy fit and angle Ball amp Socket headgear attachments ism full complement of masks supplied should include a balanced assortment of all commercially available sizes small medium and large With individual harness 3 3 3 System Configuration Accessories spares and consumables 4 ICU Ventilator 01 Adult autoclavable silicone breathing circuits 04 each a Full face NIV mask 01 each 1 2 3 1 2 3 b AI Accessories for non invasive ventilation Humidifier Servo controlled with digital monitoring of inspired gas temperature at patient end manually selectable temperature control with temperature display heater wires 02 Nos a Filter paper for humidifier for 100 uses 02 5 Power Supply 154 Power Supply 230V 50 Hz ee Standards Safety and Training 61 Should be FDA CE BIS approved product Manufacturer should have ISO 9001 certification for quality standards On site Comprehensive training for lab staff and support services till customer satisfaction with the
16. Technical Maintenance manual to be supplied in English ln cXE s Certificate of calibration and inspection from factory DeartmenSiNo OOO Equipments no B OOO BomedislAsetNo OOOO omy eS Smir ems SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS Microprocessor Controlled ventilator with integrated facility for ventilation monitoring suitable for use on adults 1 small sized adults and adolescents Should NOT be a machine working on turbine technology or any modification thereof O T O 2 TECHNICAL SPECIFICATIONS Cd 23 Standard hinged arm holder for holding the circuit ooo 22 color TFT screen 12inch or more vertical display O O O 23 Facility to measure and display S O ooo o a 3 waves Pressure and Time Volume and Time and Flow and Time b 3 loops P V F V P F with facility of saving of 3 Loops for reference y O f To Graphic display to have automatic scaling facility for waves d Status indicator for Ventilator mode Battery life patient data alarm settings clock O oom Trending facility for minimum 24 hours preferably 72 hours with minimum 5 minutes resolution for recent 24 hours 2s automatic compliance amp Leakage compensation for circuit and ET tube 2e Jroliowing settings forall agegroups O OCO OCOS E Fy Pesuwe mpkSt70cmH O
17. e a Should have the ISO certification and the copy of the same should be enclosed along with the technical bid The quoted model should have CE BIS certificate and copy of the same should be enclosed along with the technical id b User Technical Maintenance manual to be supplied in English Certificate of calibration and inspection from factory pq 3 NEN EEN et CE ees a ee NI Ooo J gt Eq tm Department SI No TANANA Eauipmemtsino B 0 0000000 Biomedical Asset Nox OOO Quantity o Smhrtems OOOO ItemName OT TABLE HIGH END SL NO SPECIFICATION Ey Technical Specifications Should be multi purpose powered electro hydraulic OT table C Arm Fluoroscopic compatible suitable for all major 1 surgical procedures including trauma orthopedic and neurosurgical complete with a corded handset with battery level indicators and moulded anti static seamless mattress oo ee caudally ee ee eee locking mechanism ee S The handset should offer controls for trendelenberg reverse trendelenberg lateral tilt flexion extension 90 230 5 degree longitudinal tabletop traverse and height functions min height around 700 800mm and max height around 1000 1200mm Should have facility to return to neutral position auto zero 6 The brakes wheels and castors should be controlled by two foot pedals 7 The table should feature an integrated stand by panel for controlling the movements in case of ha
18. high quality Color Laser printer CD DVD produced should be playable on any system Should also be USB Compatible 4 Power supply Le Power input to be 220 240 VAC 50 Hz fitted with Indian plug Resettable overcurrent breaker shall be fitted for protection mn aa Sa Standards Safety and Training hn a ae Should be FDA or CE approved product En ay Manufacturer should have ISO certification for quality standards WE On site comprehensive training for lab staff and support services till customer satisfaction with the system 5 Documentation S S o a UE User manuals to be supplied in English Bo ub xx Service manual to be supplied in English Department SI No Department Name JIPMER Emergency Medical Services EMS Upgradation Equipment SI No 43 Biomedical Asset Nox OOOO P quantity R00 Smarten SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS State of art high end colour doppler system with full digital technology for whole body applications to include both adults and paediatric which include abdominal obs gyn peripheral vascular musculoskeletal small parts imaging and endocavitary transvaginal transrectal Cardiac chest transcranial doppler Latest generation electronic phased array color doppler system with minimum 1000 electronic independent channels System should be DICOM 3 or higher version compatible and capable of being interfaced with HIS RIS PACS and connectivity to any PC
19. humidity of 2 15 90 Shall meet IEC 60601 1 2 2001 or equivalent BIS General requirements of safety for electromagnetic compatibility or should comply with 89 366 EEC EMC directive 6 Powersupply 1 jPower input to be 220 240VAC 50 Hz fitted with Indian Plug hue dpi Standards Safety and Training E eiu Should be FDA CE UL or BIS approved product Electrical safety conforms to standards for electrical safety IEC 60601 1 General requirements and IEC 60601 2 2S 2 safety of Electrocardiograms or equivalent BIS standard 8 Documentation gt S O OoOo cR x User Manual in English E wd a2 Service manual in English o P3 List of important spare parts and accessories with their part number and costing Oooo ee i Certificate of calibration and inspection Log book with instruction for daily weekly monthly and quarterly maintenance checklist The job description of LDeprtmemsiNo EDEN Biomedical Asset Nox OOOO Quy B 0 Smhrem O OOOO SL NO SPECIFICATION oa Technical Specifications Should be multi purpose powered OT table C Arm Fluoroscopic compatible suitable for surgical procedures complete with moulded anti static seamless mattress mm Ee ae Table top should have full length X ray translucent top with removable amp hn 1 Should have interchangeable head and leg sections with an auto locking mechanism BENE Table must allow for unrivalled C arm access a
20. prefabricated into disposable cartridges The cartridges cassettes may be meant for either single test or multiple tests cartridges cassettes meant for 3 multiple tests should be available in several denominations 100 tests 200 tests 300 tests etc The cartridges cassettes should have a shelf life of at least 3 three months and at least 30 days once installed into the system The analyser should measure the following parameters pH pO2 pCO2 lactate sodium potassium chloride and ionised calcium These parameters should be amenable for selection as per need through a touch screen interface The analyser should calculate the following parameters SO2 A a DO2 bicarbonate actual bicarbonate standard TCO2 and base excess The results of analysis should be displayed in the screen as well as printed out the printing unit should be in built Should have in built calibration and quality control functions Should be supplied along with an uninterrupted power supply UPS unit having at least 15 min fifteen minutes power back up surge protection and lightning protection features Should include consumables for 1 year one year i e 200 Two hundred tests per month and printer paper for a corresponding number of test reports calibration and quality control reports If the actual monthly requirement is less than 200 tests per month then cartridges of lower denomination corresponding to the total number of tests should be
21. should be capable of processing samples at a speed of 60 samples hour 3 The system should have large LCD display to have a review of all the results along with the three histograms of WBC RBC and PLT on the screen o 4 The system should have around 200 samples test result memory re The system should have autoprobe wiper to clean the sample probe automatically after sample aspiration 6 The system should use cyanide based reagent for Hgb estimation 7 The system should have an option to print results with or without histograms also with the option to print only basic 8 parameters System should have world reference Electrical Impedance method of cell counting for the reliability of the results with an integrated temperature sensor for monitoring amp compensating for shifts in room temperature The system should use the proven amp approved Volumetric Metering system of cell counting for WBC S RBC S amp PLT S for high precision of the results amp stability of the calibration The system should have a system of count amp aperture monitoring every 0 5 secs for precision amp reliability of the counts The system should be rotary valve based for the precise sample alliquoting for dilutions The system should have automatic floating thresholds for the correct separation of WBC S RBC S amp PLT S The system should give the differential count as Lymphocytes Mid population amp Neutrophils While mid populati
22. superficial imaging Hockey stick 25 mm foot print linear transducer frequency range between 6 to13 mHz for nerve block application 4 and superficial imaging D dE dmi System should have following modes ox eee 2 D M Mode Pulsed Wave Continuous Wave Color flow imaging amp color power angio a EE O Tissue harmonic imaging should be available in all transducers Digital Processing Channels 120 or more digital channels for high resolution imaging with acquisition rate of at least 50 frames per second o The system shall process a dynamic range that is at Teast sdb SSCS 30 Fine system shall support a gray scale range of 256leves 11 Broad Bandwidth Beam former technology transducers for extreme high resolution 2D Imaging 342 exenedFedofVewemgig SS 33 wtemshoudhavefaltyforgamadusmets System should have a High resolution Fully Articulating Non Interlaced flicker free antiglare Flat Panel Display of 10 inches or more System should have Image Management facility with facility for direct storage of Images and loops in the Hard Disk Drive and also thumbnail review to view amp edit Images loops and also reports HDD capacity to be specified NOE Annotation Patient id display and alpha numeric key board with track ball amp provision for reverse invert NOE Lp The system shall provide a timeline Cine function
23. supplied at no extra cost Consumable should be supplier in a staggerd manner Department SI No EquipmentSINo 200 122 HIGH DEFINITION LAPROSCOPY SYSTEM SL NO SPECIFICATION 1 Technical Specifications High Definition Three Chip Camera System 2 Camera console 220 v with universal coupler amp Autoclavablecamerahead O 1 3 Pure Digital signal with high definition video 1280 1024 native resolution 24 JgmResduon2000horzontallies Cis S5 JjBspecaltysetins S 6 integrated Flexible Scope filter 000000000000 7 Signal to Noise ratio 70db S f 8 Progressive scan technology both on camera head amp console 1 9 Brightness Control on console amp camera head S O f 10 jAerweConmloncosoe O OOO OSOS SS 11 inbuilt 16 step digital Image Enhancer on console o O 12 jpigtalzoom amp whitebalanceoncamerahead O O 13 integrated Gain shutter Enhancement with brightness control Cd 14 Two peripheral control on camera head S Pe eee NEMNNEINENNMINMMWNMNMMNNDNNNBNBPBMNMNNWN N 9 9 NWyWy 3 2 DNN 2 jVdeoOupt OO SOSS 2 Voto 2 psws amp iRGBoupt O O 3 JjOneComposteoutput S ca 3 Automatic Light source ee CSs SSSCCSC zC 3 20v30W XennBub wthonesparebub 2 Eliptical Bulb technology S
24. system Deumematon OOOO User Technical Maintenance manuals to be supplied in English a he ae Certificate of calibration and inspection Should have 3 years three years on site comprehensive warranty for all components excluding the consumables and comprehensive annual maintenance contract comprehensive AMC for 5 years five years effective from the fourth year of installation Department SI No Department Name Equipment SI No 6 instrument ref No Biomedical Asset No Qumty 8 LL Similar items PO ECG MACHINE 12 CHANNEL SL NO SPECIFICATION ED i Description of Function ECG Machine is a primary equipment to record ECG signal in various configurations 12 channels with interpretation are required for recording and analyzing the waveforms with special software fo 2 Operational Requirements LE ue 9m The ECG machine should be able to acquire all 12 Leads simultaneously and interpret them 3 oo Technical Specification PT Should acquire simultaneous 12 LEAD ECG for both adult and pediatric patients mn P2 Should have real time display of ECG waveforms with signal quality indication for each lead 2 3 Should have Artifact AC and low and high pass frequency filters Should have a storage memory of at least 100 ECGs with easy transfer by optional modem and data cord Should have full screen preview of ECG report for quality assessment checks prior to print Should have interpretation faci
25. use 26 Ventilator should have Volume Control and Pressure Controlled SIMV and PEEP Ventilator should have a tidal volume compensation capability to adjust for losses due to compression compliance 27 and leaks and compensation for fresh gas flow 2z The workstation should be capable of delivery of low flow anesthesia Ventilator should be capable of at least 120 150 L min peak flow to facilitate rapid movement through physiologic dead space in the Pressure Control mode o 130 Anesthesia Monitoring System should be modular Monitoring of vital parameters ECG 5 leads with ST segment analysis NIBP SPO2 and 2 Invasive Blood Pressure amp Spirometry with display of flow volume loops o 32 Twin temperature measurement with skin and rectal probes Two sets with each monitor Automatic identification and measurement of anesthetic agents EtCO2 O2 and N20 and MAC value FiO2 33 measurement s4 Neuromuscular Transmission Monitoring with all accessories One set with each monitor 35 continuous Cardiac Output monitoring module with accessories lt O ss zawsofgaphcsandmumeralendmg O OO 37 Should have Hemodynamic Oxygenation and Ventilation calculation package SOS Should include inbuilt Anaesthesia record keeping software facility in all OT monitor to document anesthesia event 38 using standardized menu based entries Compatible with common third party information management
26. 2 supportfeet 2 pieces T nB Screw tensioners 2 pieces 14 Traction boots Leather boots with bottom plates attached to screw tension device with a ball joint Adult 1 pair Child 1 pair 35 SumupdampwihrotstonforfiingKrchnerbowtracdon Knee support Table height adjustable radio translucent carbon fibre padded attached to adapter that can be Knee support extension bar height adjustable radio translucent carbon fibre padded attached to support port Hand operating side attachment padded height adjustable radiolucent top measuring with roller wheels Accessories stand mobile with castors frames and baskets made of stainless steel for storing small parts and extension bars Raised arm support with pad one REN UNE ONE Due HEN EMEN EMEN Ep E pc PEE 33 sSmesppotam OOO OOOO NER E a E ane Gee i ae ee 5 e ae 31 Gel pads for patient protection all types amp sizes Should have the ISO certification and the copy of the same should be enclosed along with the technical bid 3 7 1 Standards Safety and Training P d ERR US The quoted model should have CE BIS certificate and copy of the same should be enclosed along with the technical bid 4 jeumenaio OOOO User Technical Maintenance manual to be supplied in English ar 42 Certificate of calibration and inspection fromfactory C Ooo DertmenSiNo OOO EupmenslN B
27. Compatible System should have extensive Calculation software package for General Imaging obstetrics amp Vascular Imaging with 22 basic cardiac calculation software NN system should have the capability to enhance echogenicity of needles for nerve block applications amp biopsy 24 The in built battery backup time and battery life to be specified hm ie Weight of the equipment should allow easy manual portability preferably less than 5 to 7 kg 3 jwexoks OOOO 11 12 13 14 15 16 17 18 19 20 21 23 24 A mobile docking station shall be available to store and or transport the system with an option for at least three 1 active transducer ports in a convenient to access location NEC The system shall be able to be connected to external peripheral devices such as an external monitor printer and or 2 DVDR Oo i a The system shall be able to be connected to an optional footswitch for hands free operation I vp 4 1 B w Thermal Printer of latest model with CE or FDA mark PTS UPS of appropriate rating with 60 mins back up additional to in built battery back up 4 POWERSUPPLY 1 jPower input to be 220 240 V AC 50 Hz 5 __ STANDARDS SAFETY AND TRAINING boo P031 Should be FDA CE BIS approved product ln a a Manufacturer should have ISO certification for quality standards a On Site Comprehensive training for lab staff and support services till customer satisfaction with the system 6
28. DOCUMENTATION PT User manuals to be supplied in English aa ae ES Service manuals to be supplied in English Department SI No Department Name Equipment SI No M A O instrument ref No Biomedical Asset No o O e LL Similar items fT PORTABLE ULTRASOUND FOR OT SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS Should should be latest generation state of the art portable color Doppler for abdominal vascular musculoskeletal small parts basic cardiac and nerve block application with suitable evaluation and measurement packages 2 TECHNICAL SPECIFICATION a o System should be offered with following electronic multi frequency Broad Band width transducers Convex array transducer frequency range of 2 to 6 mHz for general purpose abdominal gynecological and 1 obstetric imaging a a linear array transducer 10 to 15 mHz for small parts vascular musculoskeletal nerve blocks and superficial imaging 3 phased array sector transducer 1 t05 mhz for cardiac imaging amp Transcranial doppler probe optional 5 system should have folowingmedes 0000 EN Processing Channels 120 or more digital channels for high resolution imaging with acquisition rate of at least 50 frames per second System should have Image Management facility with facility for direct storage of Images and loops in the Hard Disk Drive and also thumbnail review to view amp edit Images loops and also reports HDD capacity to be spec
29. OOOO Biomedical Asset Nor OOOO Smhrtems HIGH END OT LIGHT WITH CAMERA SL NO SPECIFICATION USENET a 1 Technical Specifications o pia OT Light an Should be dual dome LED surgical lighting system ceiling mounted type with one dedicated spring arm suspension for progressive scan HD flat panel with an integrated in light camera system Operating room surgical lighting system should provide an ideal combination of brightness maneuverability and pu shadow resolution without sacrificing color accuracy through a consistent LED technology with a unique faceted reflector design technology s should have two number of light heads per suspension Oo a pheudhwemiimm90ips O OOOO 5 chrtempemtreshoudbe4000 50K O 6 Field size diameter depth should be 6inch 12mh 7 pephoffedshoudbe30 3Simh O s itumination level should be minimum 160 000Luxeach o Jheudhwewallowolouhpand O 40 Rotation should be 360 degrees O O 3i shouted have vertical adjustment range of 0 mh 25 inh O 32 jHadeshudbestrlsbie OCO OCOS L i ea Integrated in light camera system should be integrated at the centre of one of the domes of this lighting system in 3 Minimum illumination shouldbe lt 3 Such Light and Integrated Camer
30. SITC of equipment part A Medical equipments and Part B Medical furnitures at emergency medical services casuality department in JIPMER Puducherry PART A MEDICAL EQUIPMENTS DepartmentsiNo EmipmetSNo a O O Biomedical Asset Nor LL quantity Smieiems OOOO SL NO SPECIFICATION Ere m 1 Hrechnical Specifications 1 Defibrilator shouid be Bi Phasic ight weight and atest model 2 heudmontervtalparametersanddipaytem 3 heudpintthetCGonthemalrecorders O BEEN Should work on manual and automated external defibrillation AED mode Should have manual selection up to 200 J 3 shouid be capable of doing synchronized amp asynchronized cardioversion 6 canbe operated from mains aswellasbattery O OC OCCO SOCOS 7 should have defibrilatortestingfaciity OCO 8 heudhwenoniwswepangfacity Should be a low energy biphasic defibrillator monitor with recorder having capability to arrest all arrhythmia within a maximum energy of 200 J oom Should monitor ECG through paddles pads and monitoring electrodes and defibrillate through pads and paddles r jJL un ij Should have automatic lead switching to see patient ECG through paddles or leads hz a Should measure and compensate for chest impedance for a range of 25 to 200 ohms o T nB Shoul
31. Should be FDA or CE approved product c wp c Electrical safety conforms to standards for electrical safety IEC 60601 IS 13450 hie iE 3 Manufacturer should be ISO certified for quality standards DepanmentsiNe RupmensNo pa O O OOOO LY Biomedical Asset Nox OOS Quy BO Smhrem SSCS SL NO SPECIFICATION 1 MRQURMENIS 3 Smal lightweight compact rugged defibrilator moniton o 7 2 12 lead ECG analysis program SPECIFICATIONS Simple operation dedicated therapy controls configurable options Data storage Transmission and retrieval capabilities ower A Battery Only Configuration choice of batteries P B Dual battery capability C DCPower Adaptor for transportation D Batteries should charge while device operates from Power Adaptor E Low Battery Indicator and message EHE RET HN E ae 2 ier i apr HE pug eM p REIN i L F Warm start PT G Service indicator Display LCD User selectable contrast minimum 4 secs of ECG and alphanumeric option to display one or two additional channels 5 6 Data Management Report Types Three Formats types two full capacity patient records IBN Communications PC Card Internal Modem External EIA TIA Modem Cellular Modem or serial connection 1 8 Monitor Lead Selection ECG Size Heart Rate Display Continuous Patient ae ae Surveillance System Voice Prompts and Analog ECG Outp
32. a should have a control through Touch Panel of the control equipment placed inside the operating room at documentation station nurse works station Flat Panel Monitor 3 REIN Di i ae rop T EN NER ERES RR a heudhweoptiizom of25 30 O O O O hcc SEV ieee gp NEN EE at N E 4 Should be 23 High Definition progressive scan flat panel monitors with ceiling mounted spring arm suspension to support high definition HDTV progressive scan images and should be able to support and display DVI HDTV RGBHV S Video Composite video signals The flat Panel suspension should be ready with the cables for integration of High Definition Digital DVI HDTV RGBHV High Resolution SVHS S Video Composite video signals to travel from the various sources of video like endoscopic camera room camera in light camera high definition flat panel monitors while assuring native resolution signal s Resolution should be 1600 dots x 1200 dots Progressvesan a pisseyColerssheudbei6MillonColos 5 shoul have inputs of DVI RGBHV S Video Composite Video 6 Response time shouldbe2sms 7 travel shouldbe 330 340 SSCSC S SC S SC SSSSSS 8 jwedt ksoudbe30 9 O o Bekwadtitshoddbeds 5 fe CNRC NN pc qo me s NBN Shoul
33. ating continuously in ambient temperature of 30 deg C and relative humidity of ENNUNE ca a M MR EBEN dudes eee 3 9096 NDA EMEN ee 2 e EE s powes LL 1 JPower input tobe 220 240VAG SURE OO O OO O O O OSOS Exp e IT l 6 standaras Safety and Trainin OZ OOOO i J should be FDA or CE approved product O O OSOS 2 Electrical safety conforms to standards for electrical safety IEC 60601 1 General Requirements Manufacturer should be 150 certified for quality standards O o HN Certified for meting IEC60601 2 24 Particular requirements for the safety of infusion pumps and controllers Ls Should meet IEC 529 Level 3 and 4 IP3X spraying and splashing water for enclosure protection water ingress 6 Electrical Safety Classification Class I Il Type CF and Internally powered equipment Certified for meeting IEC 60601 1 4 Medical electrical equipment Part 1 4 General requirements for safety 7 Collateral Standard Programmable electrical medical systems 8 Comprehensivewarrantyfor3yearsandprovision of AMCfornext5years O Should have local service facility The service provider should have the necessary equipments recommended by the manufacturer to carry out preventive maintenance test as per guidelines provided in the service maintenance 7 Documentation gt OE Ecc qb i Certificate of calibration and inspection from fa
34. by screw handlefromfootend a Tubular head and foot end bows of suitable thickness of stainless steel 5 Should have one 1V rod with own hooks chromium plated SSCS 6 heudhavesbtforiVrodatexchofthefarcomes 7 Should have antislip PVC stump of durable quality for Tegs a Finish should be multiple layer pretreatment and epoxy powder coating To be supplied with rubberized coir foam mattress of high quality 10 cm thick Covered with waterproof anti microbial upholstery Pillow soft rubberized foam with antimicrobial cover 20 Colour should be Ivory Grey dj a 3 Dimensions should be around 2100 mm L x 850 mm W x 50cm sleep surface 2 f Standards Safety and Training Lee Should have the ISO certification and the copy of the same should be enclosed along with the technical bid The quoted model should have CE BIS certificate and copy of the same should be enclosed along with the technical bid BEN 3 Documentation S O hisce User manual to be supplied in English pu AR M Department SI No Ss EquipmentSINo 28 Biomedical Asset Nos C aay m Sd Similar items ooo SL NO SPECIFICATION Technical Specifications hould be four section bed with mattress base a Js E o gd The system should be electrically operatable and adjustable for heights trendelenburg etc P3
35. cessories spares and consumables The system should be supplied with necessary prerequisites amp Startup Kits Normal amp Abnormal QC amp calibrators Halogen bulb set 10 Nos One extra sample tray and reagent tray if they are not fixed to equipment Reaction cuvette one spare if fixed and if disposable cuvette it should last atleast for one 5 The instrument should work on tap water available If any special treatment required then treatment plant should be provided 1 2 3 The system should be supplied with a compatible Desktop PC microprocessor with speed not less than 3 GHz 4 GB 28 RAM 500 GB HDD USB keys board scroll mouse multimedia kit CD DVD RW Drive with 17 LCD monitor with Autoclavable autopipettes to be provided with each unit individual prices for following items itemnos 2 6 1 amp 2 6 2 should be specified in the price bid fee eC 7 ed I s homses SSS peu ms e poos 6ms I per cup e O O 8 aee UL a pozo 6ms LL e pomioiXoM 6ns o Jreagents tobe provided witheachunit 94 jdwe GODPOD io0Utets O O 32 Jue dotes os ereatinine sooress O OCO O oS oa jWimbiT amp D 2000tests Each OOOO 35 me 3 lots 6 ek soos O 97 fe
36. computer 3 Should be field upgradeable to next generation system on site All new softwareshould be upgraded free of cost for at least 3 years Speckle reduction filter real time spatial compounding frequency compounding or better technology should be available in convex and linear probes for better resolution and penetration 2 d 1 Technical specification i a Latest generation electronic phased array color doppler system with minimum 1000 electronic independent channels i aa 256 gray shades or more for sharp contrast resolultion System should be offered with following electronic broad band width transducers o ae ee MENT t Nea OOO 2 Broad band Linear array tranaducer frequency range of 6 to 12 MHz suitable for vascular and small parts oe eee LEA QUNM MM AV P A Phased array sector probe of 2 to 5 MHz for cardiac studies a probe Transvaginal Trans rectal 5 9 MHz or more Endocavitary probe should have biopsy el facility with needle guides 4 Harmonic Imaging should be available in all probes with the following modes and settingfor Pf mmuhamone OOO Contrastharmonic S O P HameneAndo LL Harmonic imaging in power doppler imaging mode for improved sensitivity and specificity in differentiating blood agent from tissue Gain control in two dimensions for additional level of flexibility to image quality control Real time high frequency 2D for higher resolution and low frequency Doppler for hig
37. ctory List of Equipments available for providing calibration and routine maintenance support as per manufacturer documentation in service technical manual 2 83 User Manual in English PT Service manual in English Log book with instructions for daily weekly monthly and quarterly maintenance checklist The job description of the hospital technician and company service engineer should be clearly spelt out 5 1 6 List of important spare parts and accessories with their part number and costing mm hE aa User list to be provided with performance certificate i 8 Performance report in the last 5 years from major hospitals should be enclosed Department SI No Department Name JIPMER Emergency Medical Services EMS Upgradation EquipmentSINo la oo O instrument ref No Biomedical Asset No 000000 O C any oooO Similar items SPECIFICATION i o The portable ventilator should be light weight lt 10 kg oa aaa Should be microprocessor controlled hea ee ee Should operate with main electric supply as well as with battery 3 Should be able to work both with cylinders pipeline amp room air Connectors and high pressure tubing of appropriate length to be supplied 4 shouid have turbine Venturi jet mixing technology for supplying air lt oxygen mixture 5 should have following modes ofventilaton SCS 6 evry assist Control SIMV PS PEEP amp SIMV pressure control SIMV PC
38. d have a built in strip printer thermal recorder BEEN Should have charging time of less than 5 seconds for maximum energy Charging indicator should be present as shouid have bright display for viewing messages and ECG wovefommfor seconds 16 should have external paddles with paddles contact indicator for good paddle contact a7 singe Adult and pediatric paddles shouldbe available OC 18 should have event summary facility for recording and printing atleast 250 events and SO waveforms 19 shout have a battery capable of usage for at least 90minutes or 30 discharges 20 shout be capable of printing Reports on Event summary configuration self test battery capacityetc 21 shout have facility for self test check before usage and setupfunction a E Should be capable of delivering energy in increments of 1 2 joules up to 30J and increments of maximum 503 thereafter 33 jPowerimputtobe220240VAC SOHzndanplug Pee ee 2 system configuration Accessories spares and consumables Patient ECG Cables 02 Gel bottle 2 Nos Should have the ISO certification and the copy of the same should be enclosed along with the technical bid Documentation Two numbers of complete User Technical Maintenance manuals to be supplied in English Certificate of calibration and inspection from factory Downtime Pr
39. d have the ISO certification and the copy of the same should be enclosed along with the technical bid 5 The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid ae a o3 gue EBENE CNN Training should be provided for users and biomedical engineers User Technical Maintenance manual to be supplied in English Certificate of calibration and inspection from factory DepartmentSINo Equipment SI No 100 BiomedialAset Noi O OOOO Quantity 2 Similar items Item Name PORTABLE OT LIGHT SL NO SPECIFICATION S 7 Should have intensity control from 40 100 Should have emergency power unit having in built CVT with automatic change over from mains to battery mode in the event of power failure 9 Battery should provide atleast 60 minutes back up Power input suitable 220 240V 50 Hz AC Single phase fitted with appropriate Indian plugs and sockets Standards Safety and Training Should have the ISO certification and the copy of the same should be enclosed along with the technical bid The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid User Technical Maintenance manual to be supplied in English Certificate of calibration and inspection from factory DoeetmensiNe EupmensNo a SSS Biomedical Asset Nox OOOO quantity fe 0 Smhrem SL NO SPECIFICATION
40. d not be delivered when there is a leak in the circuit 7 18 The system should incorporate a connector which can allows connection of hand switches equipped with any of the international accessories 1 1 1 1 1 1 1 1 rope m system should have the option of operating Monopolar cutting and coagulation by using both hand and footswitch 30 rhe system should be supplied with standard accessories for both Monopolar and bipolar Sa a 3 system Configuration Accessories spares and consumables 2 Bpoarforepswiheable2nos O OOOO S 3 Umposrhendlewthesbled0Nos O a mewphtesndcsblein O O 5 erefseims LL 6 Jjemodstin 7 jetih2ns LL 8 Jn wthin Bees genet ge m MM Disposable patient plate 100 nos _ ees Standards Safety and Training mera Should have the ISO certification and the copy of the same should be enclosed along with the technical bid L9 3 The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid I Etha shout be een forse and engineers MM raining should be given for users and engineers rue MMmQ E dq ou s Two numbers of complete User Technical Maintenance manuals to be supplied in English PT Certificate of calibration and inspection from factory DBeprmensiNo
41. dNos OOOO 3 Jvemesmedeisomenmgh Nos OOOO a grboemdroxdegestubig Nos OO 5 mewssewesiimm No O 6 fedwerijsmmaNo SSS 7 mewsseeesSSmm4Nos O OOOO 8 eens pramdaltiplOmm Nos 9 meens pwamdaltismm4Nos Trocars washer 5 mm 100 Nos Trocars washer mm 50 Nos aproscopic biopsy forceps 5 mm 2 Nos aryland dissector 5mm with unipolar diathermy 4 Nos 0 pe p E duree sa ee NE 14 Atraumaticgraspers 5mm 2NOS S SO 15 Metzenbaum scissors 5cm with unipolar diathermy 4 Nos o O 16 Fanretractors5mm2Nos S SOS 17 laproscopic cautery lead 4 Nos S S 18 Suctionirrigation device with two way valve 2 Nos S O 19 Lshapedhookelectrode5mm SS SY 20 laparoscopicbowelgrasper5mm lengih33 36 cm 2 Nos Laparoscopic suction cannula 10 mm 2 Nos 29 japtonderaimer 00000000000 so jerderemede TS d 31 Sterilization tray with cover 3 x 1 usable with plasmasteriliserforlaparoscopesandlightcables DENN KNIE A AP eT 8 Standards Safety and Training o are Should have the ISO certification and the copy of the same should be enclosed along with the technical bid The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the 2 technical bid 9 Documentation S O pP GL x i User Technical Maintenance manual to be supplied
42. djustments on spectral modes auto angle correction filter adjustment base line and EH sweep speed adjustments mE Real time panoramic imaging to have an extended field of view of structures 34 System should have facility for separate 2D quick scan auto 2D optimization Doppler Quick Scan auto baseline p and PRF adjustment RE el System should have automatic real time quantification of doppler parameters Virtual Convex Trapezoid format with both Linear as well as convex Probes should be available 3 SYSTEM ACCESSORIES AND CONSUMABLES Oooo ooa Colour Laser printer with direct printing connectivity for printing stored images 5 Online UPS with capacity for 30 mins back up of all functions of the equipment i e performing ultrasound procedure exposure onto films 3 100CDs and 100 DVDs a Color printer paper 500 sheets Computer should be preloaded with licensed latest window operating system and full fledged image management 5 software capable of storing still images recording loops archiving printing in various formats Making CDs DVDs post process image manipulation etc pepecempvl PEDI ER 4 powes o Power input to be 220 240 VAC 50 Hz fitted with Indian plug Resettable overcurrent breaker shall be fitted for protection ve pe XE T Standards Safety and Training D db xw Should be FDA or CE approved product Oooo o 04 Manufacturer should have ISO certification for quality standards
43. ecomyewtensptemd OOOO Guide wires 2 types 0 025 F 0 035 F in diameter length 450 cm non kinkable with stripes to detect movement 5 ENSE VE Balloons 11mm diameter and wire guided 5 PT Cleaning channel and suction channel knobs 10 each 9 Xenon bulb 1 No 3 Standards Safety and Training BEN Should have the ISO certification and the copy of the same should be enclosed along with the technical bid L9 The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid 4 Documentation S O bs cd Roy User Technical Maintenance manual to be supplied in English BeartmensiNo RupmenslNo pa O OOOO BomedislAsetNo LL Qmy Smir em SL NO SPECIFICATION Technical Specifications The unit should have microprocessor based control Should have provision for use by 2 surgeons simultaneously S hould have provision for three types of cut and four modes of coagulation Should have both bipolar and Monopolar options Should have both hand and foot controls Should have underwater facility 7 Monopolar mode should have cutting spray desiccation and fulguration Output power should be greater than 300 W Power efficiency rating should be more than 96 0 2 3 4 5 8 The system should provide high patient safety from burns caused on the patient s skin due to leakage in the electric current The power shoul
44. en 2 25 ul of sample a For Pediatric samples minimum dead volume of sample up not more than 20 ul EMEN Reading volume should be 150 ul or less Must have 7 or more step Cuvette cleaning facility and no carryover i he Must have minimum water requirement of not more than approximately 20 liters hour only Should be capable of performing eEdpoint Kinetic turbidimetric homogeneous and bichromatic assay facility o T z Should have a good real time QC programme with l J graphs Printout of QC charts amp reports a a Spectral Range 340 to 750 nm by diffraction grating optics 5 The Light Source Halogen Xenon Lamp should have low cost and very long life of not less than 24 months Low power consumption less than 1000 VA 2 26 Equipment should be supplied with external water treatment system as required 27 xtensive Data Management Software A The equipment should be supplied with compatible programmable Windows based comprehensive data processing amp management system E 27 2 Graphical user interface software and should have LIMS Capability 27 3 Should have complete back up of the database for calibration control and patients sample results 27 4 At least 10 000 patient result storage and multitasking facility on computer5 27 5 Should have provision for barcode reading facility 27 6 Personal Computer 27 compatible Operating system and compatible LASER printer for documentation System Configuration Ac
45. er Technical Maintenance manual to be supplied in English Certificate of calibration and inspection from factory bo NM NBN X O 3 Oo o o oaf ees p o r n RENNES NNI Deng pup NEN NNI Department SI No EupmenslNo ig O OOOO instrument ref No Biomedical Asset Nox OoOO Qmy Bo Similares OOO SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS State of art high end colour doppler system with full digital technology for whole body applications to include both adults and paediatric which include abdominal obs gyn peripheral vascular musculoskeletal small parts imaging and endocavitary transvaginal transrectal Cardiac Chest transcranial doppler Latest generation electronic phased array color doppler system with minimum 50 000 electronic processing channels System should be DICOM 3 or higher version compatible and capable of being interfaced with HIS RIS PACS and connectivity to any PC computer etc in DICOM format 3 Should be field upgradeable to next generation system on site All new softwareshould be upgraded free of cost for at least 3 years Speckle reduction filter real time spatial compounding frequency compounding or better technology should be 4 available in convex and linear probes for better resolution and penetration The system shall have automatic system optimization One Button for Both B Mode and Doppler 02 Technical specification DE Latest generation electronic
46. es i 1 Must have ISE unit for Na K Cl measurement a Assays should be possible in serum plasma urine CSF Whole blood hemolysate 5 Must have self diagnostic tests with error message amp online display oo l 6 Must be programmable for all test menus amp state of the Art Work Station EHHJ ose ec reagents Must have continuous loading of samples with on board capacity of at least 80 permanent cuvettes with 5 years of 2d e 77 c 77 uL PEL 93 jhewdhwewakwaytmeuptodhous 10 Should have Pre amp Post Auto dilution of samples andRerunCapabilityforoutofrangesamples Should have both internal amp external Probe cleaning washing facility EE NIE E Log m Should accommodate at least 50 samples in single run Probes should be long life of at least 24 months 13 Calibration must be Linear Nonlinear factor exponential spline loglogit or with Auto diluted series of stock calibrator nes Should have calibrator and control with repeat facility Reagent Refill message amp monitoring should be available a a ce 6 RENE ERE a Should have facility for automatic printout of reports amp full patient demographics Proble Dispensers must have level detectors amp separate probles for Samples amp reagents R1 amp R2 uvette mixing by variable speed at least two stieeres for immuno tubidometry tests a3 Must typically use betwe
47. evels selectable from 300 500 900 mmHg Must Work on commonly available ISI CE FDA APPROAVED CERTIFIED 20 30 50 60 ml Syringes with accuracy of minimum of 2 or better Automatic detection of syringe size amp proper fixing Must provide alarm for wrong loading of syringe such as flanges out of slot disengaged plunger unsecured barrel etc 7 8 Anti bolus system to reduce pressure on sudden release ofocclusion Should have comprehensive alarm package certified for meeting IEC 60601 1 8 Medical Electrical equipment Part 1 8 General requirements for safety collateral standard Alarm systems including Occlusion limit exceed alarm Near end of infusion pre alarm amp alarm Volume limit pre alarm amp alarm KVO rate flow Low battery prealarm and alarm AC power failure Drive disengaged air in line and preventive maintenance Rechargeable Battery having at least 5 6 hour backup for about 5ml hr flow rate with 50ml syringes Larger battery life and indication of residual life will be preferred 3c 2 1 System Configuration Accessories spares and consumables Syringe Infusion Pump 01 Mounting device Docking Station for two or four pumps as per requirement so as to enable to power up to 2 4 pumps with one power cord when mounted on IV pole 01 Environmental factors Shall meet IEC 60601 1 2 2001 Or Equivalent BIS General Requirements of Safety for Electromagnetic The unit shall be capable of oper
48. ght weight vinyl lead aprons with 0 5 mm lead equivalence certified by BARC or AERB or ISO 2 Two Nos Oo a Universal sterilisable covers for the image intensifier container Carc and tank uni 5 sets of 3 covers a o Standards safety and training Should have the ISO certification and the copy of the same should be enclosed along with the technical bid Training should be provided for users and biomedical engineers 5 The quoted model should have FDA CE BIS and the copy of the same should be enclosed along with the technical bid Documentation nn hn x Two numbers of complete user technical maintenance manuals to be supplied in English hn i a Certificate of calibration and inspection from factory Department SI No Department Name JIPMER Emergency Medical Services EMS Upgradation Equipment SI No Biomedical Asset No o O Quantity fe Similar items ff SLNO SPECIFICATION 1 TECHNICAL SPECIFICATION The instrument should be an open system discrete random access clinical chemistry analyser capable of all routine 1 STAT and special biochemical tests including specific proteins therapeutic drugs TDM drugs of abuse immunotubidemitric Assays and user definable applications in Plasma Serum or Urine The Equipment should be configured as per consignee requirements gt Equipment must have atleast 200 tests in chemistry in a throughput of not less than 300 tests per hour including electrolyt
49. her sensitivity in all probes Frame rate should be 300 FPS or more The frame rate in triplex mode should not be less than 12 frames per seconds Steerable PW CW on all phased array probes High definition acoustic zoom for enlarging sections of 2D and color flow images with more acoustic information for 0 greater clarity and detail while maintaining an optimal frame rate T Modes 2D B Mode B B Mode M Mode steerable PW CW Doppler color Doppler B M Mode B PW Doppler B CW Doppler B Power Angio B and Power Angio should be available 12 Monitor should be High resolution non interlaced LCD Color monitor of 17 inches or more with tilt and swivel facility to view in all angles and all light conditions nB Color flow imaging for E ua o Increased lateral amp spatial resolution auum Detection of even subtle areas of turbulence displaying a more physiological blood flow appearance without loss of frame rate i I Color flow with capability of automatically picking up color flow as a function of focal depth PT Tissue colorization B Color for improved contrast resolution 15 Should have facilities and application software for adult abdominal obs gyn peripheral vascular musculoskeletal small parts imaging and endocavitary applications All application package should be built into the system 16 Cine loop facility both frame by frame and in cine mode with a memory for atleast 300 2D color images review and a
50. hetic material Should have bedsore prevention safety features 19 Mattress should be radiolucent to allow radiography using portable X ray machines 0 Power input to be 220 240VAC 50Hz as appropriate fitted with Indian plug SSCS UNI Sea eS T 2 system Configuration Accessories spares and consumables po 1 lCUBedmainframe 01 S 2__BedEnds detachable OlparOSOSC SCSCSCSCSCSC lt CSCS o a Articulated half length tuck away side rails 04 Nos 4 VRos Q No 0000000000000 Ex 03 Standards Safety and Training ta Should have the ISO certification and the copy of the same should be enclosed along with the technical bid a ie Se The quoted model should have CE BIS certificate and copy of the same should be enclosed along with the technical bid 4 Documentation S S Ei casu User manual to be supplied in English Eb d a Certificate of calibration and inspection from factory
51. hould be FDA CE BIS approved product Oooo eee Manufacturer should have ISO certification for quality standards ee On Site Comprehensive training for lab staff and support services till customer satisfaction with the system 6 DOCUMENTATION psc cu a User Technical Maintenance manuals to be supplied in the English 1 2 Certificate of calibration and inspection DBeprtmemsiNo EupmensNo O O OOOO SSS Biomedical Asset No OOOO Quy pa Sd Smarten OOOO ItemName NFUNONEUMR SL NO SPECIFICATION Operational Requirements The syringe pump should be programmable user friendly safe to use and should have battery back up and comprehensive alarm system 2 Demonstration of the equipment is a must p2 ee Technical Specifications a ara Flow rate programmable from 0 1 to 200 ml hr or more in steps of 0 1 ml hr with user selectable flow set rate 1 option Bolus rate should be programmable to 400 500 ml hr or more with infused volume display Reminder audio after 5 every 0 5 ml delivered bolus SAVE last Bolus rate even when the AC power is switched OFF E gel s 1 Display of Drug Name with a provision of memorizing 10 15 names by the operator Keep Vein Open KVO must be available 1 0 ml hr or set rate if lower than 1 0 ml User should have choice to disable KVO whenever desired Dc d 5 O Selectable Occlusion pressure trigger l
52. ified Display Annotation Patient id display and alpha numeric key board with track ball amp provision for reverse invert faciy eem should have a High resolution Fully Articulating Non Interlaced flicker free antiglare Flat Panel Display of 10 inches or more 0o 7 The system shall provide the user with a zoom function DER c un MM MM 18 gray scale resolution NEN E ee MM 19 color frequency range to be specified The system should have gate adjustments on spectral modes auto angle correction filter adjustment base line and 20 sweep speed adjustments I adum 3 Image Archival Inbuilt CD DVD writer Flash drive with the facility to transfer images DICOM 3 0 Compatible System should have extensive Calculation software package for General Imaging obstetrics amp Vascular Imaging with 23 basic cardiac calculation software system should have the capability to enhance echogenicity of needles for nerve block applications The in built battery backup time and battery life to be specified 26 Weight of the equipment should allow easy manual portability preferably less than 5 to 7 kg 3 ACCESSORIES A mobile docking station shall be available to store and or transport the system with an option for at least three 1 active transducer ports in a convenient to access location Ld The system shall be able to be connected to external peripheral devices such as an external monitor printer and or 2 DVDR I 3 The s
53. in English DepartmensiNo SSCS RupmnsNo Bi O OOOO Biomedical Asset Nor UL CO amy ao Smiertens OOOO SL NO SPECIFICATION Poa Technical Specifications Roe upeGiope Add OOOO Lg e Angulations of tip up at least 180 degrees and down 90 degrees with right and left movement of at least 100 100 degrees 5 meriontebedimeteroflesthani mm O O C O 6 Distalenddiameter ofnotmorethantomm 7 j msrumentchemelofmorethanz8mm O OOOO 8 Workinglengthofnot less than 1100mm SSS SOS o should be compatible with the video system specified O C OC FS Pa LENIN SMMMMEUMMMMML an 2 Video processor with light source amp Monitor 1 jPowersuply20034OVA C ooo 2 jPAtpevidosgnl OO O O O OOS 3 Controls for color adjustment to enhancement and balance settings f a controls to freeze images enhance a portion of frozen image room amp post processing boo P 5 Patient and physician data input key board 6 jOpemtesonXemnlmp SS SSS xr Jp mergency lamp 8 compatibility with the gastro scope and colonoscope duodenoscope and Enteroscope SSS o 8 25 Le colour monitor withxGAresolution O o ee es ee a RR NES system Configuration Accessories spares and consumables O a jBeyfotepsdexh OOOO 2 rorgnhodygrsper pasetnpe z OO OO O OSOS a J standard tip conulai2 ypes 10ean OOOO 5 Peyp
54. ity hygienic mattress with straps for fixing 0 Should hev place for keeping oxygen cylinder B type in the trolley at the bottom of the trolley ln gti Should be provided with bumpers at four corners BEN Should have good quality stainless steel collapsible side rails and I V rod should be provided with the trolley 13 Should have pneumatic step less range of adjustment for foot section back section Trendelenberg and reverse Trendelenberg position Should have central breaking system with steering facility and bumpers at all four corner Facility for fixing IV road 14 and fixing accessories monitor Infusion pump etc Good Quality hygienic mattress with straps for fixing Place for keeping oxygen cylinder in the trolley Good quality SS collapsible side rail and I V Rod should be provided with the trolley 5 trendelburg amp reverse position Hydraulic controlled 16 Trolley should be CE marked and manufactured as per ISO quality standards hn 7 Should be supplied with patient shifting board roller type Department SI No Department Name JIPMER Emergency Medical Services EMS Upgradation Biomedical Asset Nox OOS Quantity Smhrtems SL NO SPECIFICATION b 1a ire bed should have 2 section top made up of CR sheet 5 Frame made of rectangular square mild steel section of size and section suitable to provide structural strength 20x20mm 1mm thick s Back rest section to be maneuvered
55. lity of the amplitudes durations and morphologies of ECG waveforms and associated rhythm for adult and pediatric patients I dg Should have alphanumeric keyboard for patient data Entry Virtual or hard keys Fx wu 8 Should have high resolution 200 dpi x 500 dpi on 25mm sec speed digital array A4 size printer Should have report formats of 3x4 6x2 Rhythm for up to 12 selected leads 12 Lead Extended measurements 1 minute of continuous waveform data for 1 selected lead EDBEVE Should have battery capacity of at least 30 ECGs or 30 minutes of continuous rhythm recording on single charge i Sheudbesbietebeconnededto HIS IAN Wireless LAN Optional 32 should display ECG on LCD TFT Display of 640x460 pixel resolution 33 USB support optional for storage on external portable memories 34 Multimode of ECG storage capability on floppy min 2 150 ECG on internal fash memory Li E ZU AMD EKMMMDN QUNM rM Lh Em FEIN FER 3 Chest Electrodes Adult set of six 2 sets PTA Chest Electrodes Pediatric set of six 2 sets 5 __ Limb Electrodes set of 4 2 sets 6 Thermal paper A4 size for 500 patients 5 Environmental factors SOS The unit shall be capable of being stored continuously in ambient temperature of 0 50 deg C and relative humidity 1 of 15 90 A The unit shall be capable of operating continuously in ambient temperature of 10 40 deg C and relative
56. me 3 Ows os cholesterot gt sXDtes 39 6 59e 340 Jiron 3o 91 r totatprotein 300tsS 92 ju S8otes 343 Jer stes 944 wb S00 tests 345 eiyeated Hb kt SUDtes OO OOOO 936 JWWiclbrtr LY a Me 30mwthexhui OOOO b Mew 3Omwthexhui O 347 Jac tnormal i30 mwthexhunt O 9348 Jjocghmrmaj 300 miwthexhust O Dee ee et ico Standards Safety and Training a Should have the ISO certification and the copy of the same should be enclosed along with the technical bid NN V The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid Adequate training should be provided for users and biomedical engineers at the site of installation Se E hy Re x User Technical Maintenance manual to be supplied in English ae Certificate of calibration and inspection from factory should be generated along with shipping document Department SI No RupmensNo B O LL Biomedical Asset No OOOO Quy o Smhrem SL NO SPECIFICATION 1 Should be a fully automatic haematology analyser providing 18 parameters including a 3 part differential with user definable settings to have either RDW CV or RDW SD Sn ee a The system
57. nd kidney break positioning without the need to move the patient Should offer controls for trendelenberg reverse trendelenberg lateral tilt flexion extension 90 230 degree 5 longitudinal tabletop traverse and height functions min height around 700 800mm and max height around 1000 1200mm 6 The brakes wheels and castors should be controlled by two foot pedals Oooo ee ED The table stem should be located under the middle of the back section making the tabletop eccentric Table should be able to carry heavy patients and have a capacity of up to 300kgs with an option for width extension of obese patients o 9 Table should also be suitable for tall patients and have a length of at least 2000 mm Table should offer low minimum height enabling the surgeon to operate even when seated Range 2 to 2 5 feet EN P oau The table should have divided leg section with mattresses arm board amp universal clamp System Configuration Accessories spares and consumables 1 Thetableshould be supplied with following necessary accessories including knee crutches 2 jAmsupprs 2no S SY 3 jeelhedpads 1pair O O S SOS Oooo oo a Patient positioning gel strap 200 250cms 1no 5 HandSurgeryBoard 1 0 6 jBevtedArmmSuport 2 S SY 7 Padded head shoulderand arm rest 1seteah O O OSS S 8 Padded lateral support and shoulder supports tset oS O f 9 Appropriate accessories camp OO O O O OSOS
58. ndset loss or battery failure mn 8e The table stem should be located under the middle of the back section making the tabletop eccentric Table should be able to carry heavy patients and have a capacity of up to 300kgs with an option for width extension of obese patients oom Table should also be suitable for tall patients and have a length of at least 2000 mm RANGE 2 2 5 FEET D ue RD Table should offer low minimum height enabling the surgeon to operate even when seated hn ae The table should have divided leg section with mattresses arm board amp universal clamp B Should have facilities for manual operations in case of power failures fo 2 System Configuration Accessories spares and consumables hm he aa The table should be supplied with following necessary accessories including knee crutches Arm supports 2 nos EN NE eae 3 jeelheelpads 1 pair o 4 Patient positioning gel strap 200 250cms 1no 5 HandsurgeryBoard 1 S SY 6 X BevtedArmSuport 1 S S 7 Paddedhead shoulder and arm rest 1seteach oo O 8 Padded lateral support and shoulder supports tset S O 9 Appropriate accessories clamp o SOS 10 Boot type stirrups for lithotomy poston 1 Telescopic extension bars made of chrome nickel steel with traction bars installed so as to be pivotable making possible trouble free intra operaative use of image intensifier in AP lateral and oblique planes 2 pieces 3
59. o ag js peckle reduction technology or higher technology to reduce artifacts and to improve image contrast 0 a The system shall provide the user with a zoom function The system shall allow the user to scan with at least three simultaneous focal zones in B Mode in order to maximize boka coe T The system shall have to perform color Doppler examinations with all transducers during a clinical procedure The UENTM o ood M The system should have gate adjustments on spectral modes auto angle correction filter adjustment base line and LJ alam o e UU o T zB Image Archival Inbuilt CD DVD writer Flash drive with the facility to transfer images 24 DICOM 3 0 Compatible System should have extensive Calculation software package for General Imaging obstetrics amp Vascular Imaging with 25 basic cardiac calculation software o 26 system should have the capability to enhance echogenicity of needles for nerve block applications 1 2 The in built battery backup time and battery life to be specified 2z Weight of the equipment should allow easy manual portability preferably less than 5 to 7 kg 3 j Accessories S O A mobile docking station shall be available to store and or transport the system with an option for at least three 1 active transducer ports in a convenient to access location aM The system shall be able to be connected to external peripheral devices such as an external monitor printer and or 2 DVDR
60. on should include Eosinophils Basophils amp Monocytes System should not require any daily maintenance except automatic daily shutdown The system should automatically give an alarm to the operator for doing the maintenance The system should use high intensity LED for Hgb estimation amp not the lamp The system should have low cost per test All reagents required should be available locally from the company or its authorised distributors The company should have an original external software for the system to be provided if required by user at an extra cost The manufacturer of the system should have a world wide reputation for high quality amp reliable system amp the Indian distributor should have a wide network of trained technical service amp application support persons Should be supplied with consumables to run 20 000 tests twenty thousand free of cost for the first year A separate price quoted for 20 000 tests year for next 2 years should be provided Three year warranty and comprihansive ANC for 5 years LoeprmensiNo EupmenslNo Ig O OOOO LL Biomedical Asset Nox OoOO Quy Bo I Smhrtem OOOO SL NO SPECIFICATION Should be a point of care machine able to perform blood gas analysis on heparinised whole blood samples and give out a report in less than 2 min two minutes time Should be a modular system wherein all reagents electrodes sensors and necessary mechanical parts are 2
61. on rate of at 5 least 50 frames per second 6 Thesystem shall process a dynamic range that is at least I5Odb S O 7 Thesystemshallsupportagrayscalerangeof256levels S O 8 Broad Bandwidth Beam former technology transducers for extreme high resolution 2D Imaging 9 j ExendedFieldofViewlmaging S 10 system should have facility for gain adjustments System should have a High resolution Fully Articulating Non Interlaced flicker free antiglare Flat Panel Display of 10 inches or more System should have Image Management facility with facility for direct storage of Images and loops in the Hard Disk Drive and also thumbnail review to view amp edit Images loops and also reports HDD capacity to be 80 GB Display Annotation Patient id display and alpha numeric key board with track ball amp provision for reverse invert facility The system shall allow the user to scan with at least three simultaneous focal zones in B Mode in order to maximize gray scale resolution The system shall have to perform color Doppler examinations with all transducers during a clinical procedure The color frequency range to be specified system should have gate adjustments on spectral modes auto angle correction filter adjustment base line and sweep speed adjustments Image Archival Inbuilt CD DVD writer Flash drive with the facility to transfer images USB DICOM 3 0
62. ovision for replacement of table in case a table remains unworkable for more than a week NONU NE eoo cau m ENENK NER ee p cg ae s L p 5 The quoted model should have FDA CE BIS certificate and copy of the same should be enclosed along with the technical bid HE E NE E cu pod se DepartmentsiNe SSCS Equipments No a O BomedislAsetNo OOOO Quy E Smir ems SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS Capability of measuring displaying and storage of patient data and printing and networking capabilities Ooo a NE Should be compatible with third party Hospital information systems 2 TECHNICAL SPECIFICATION Minimum 12 inches multi colored TFT display screen Modular Design Capable of simultaneous display of Six waveform and eight digital parameters with configurable design Es pp NEN p EOS es es Combination of single dual and multi parameters module modes D 5 Parameter modules freely exchangeable between all the monitors a me Multi Channel up to 12 leads ST segment analysis 7 Facility to monitor and display ECG respiration NIBP SPO2 with pleth EtCO2 with capnography Temperature Cardiac output amp IBP hn 8 Automatic arrhythmia detection amp alarm for standard and lethal arrhythmia E 539777 p J We 2 Should provide hemodynamic oxygenation ventilation calculation package Should have drug calculation package rend of at least 24 hours
63. parameters Virtual Convex Trapezoid format with both Linear as well as convex Probes should be available SYSTEM ACCESSORIES AND CONSUMABLES P001 Colour Laser printer with direct printing connectivity for printing stored images 5 Online UPS with capacity for 30 mins back up of all functions of the equipment i e performing ultrasound procedure exposure onto films 3 100CDs and 100 DVDs hn i a Color printer paper 500 sheets PC based Peripheral system should comprise of dedicated computer at least 400 GB storage space Hard disc with 4 The system shall be capable of supporting color Doppler imaging on all phased linear motorized 3D and curved array transducers Color Power Angio imaging which enhances visualization of blood flow in very small vessels and tissue vascular beds shall be supported Spectrum Imaging Both PW and CW Doppler Modes should be available Doppler sample volume size shall be adjustable from 0 5 20 mm The system should have gate adjustments on spectral modes auto angle correction filter adjustment base line and sweep speed adjustments Real time panoramic imaging to have an extended field of view of structures System should have facility for separate 2D quick scan auto 2D optimization Doppler Quick Scan auto baseline BE EM GB RAM or more with a Microprocessor speed of more than 3 00 GHz frame grabber incorporated All Software Inclusive interfaced with the machine with DVD writer and a
64. phased array color doppler system with minimum 50 000 digital processing channels erate more for ep eoa eoo an 256 gray shades or more for sharp contrast resolultion 3 System should be offered with System should be offered with following electronic broad band width transducers gt electronic broad band width transducers iE grond band convex amay maneducey with frequency range of 1 6 MHz suitable for general purpose abdominal BEBE ene nT 2 Broad band Linear array transducer Sed nd range of 3 to 12 MHz suitable for vascular and small parts BN Qu ed 3 Broad band Linear array tranaducer frequency range of 3 to 17 MHz suitable for vascular superficial En musculoskeletal superficial and small parts applications P 4 Phased array sector probe of 2 to 5 MHz 5 Endocavitary probe Transvaginal Trans rectal 5 9 MHz or more Endocavitary probe should have biopsy facility a with needle guides HEN 6 3D volume acquisition transducer of 2 to 6 MHz for 3D and Live 4D imaging 4 Harmonic Imaging should be available in all probes with the following modesandsettingfor P jJHsseharmone ooo jJCemestharmonic S HarmonicAngio S Quantification ofharmonicsimaging S Harmonic imaging in power doppler imaging mode for improved sensitivity and specificity in differentiating blood agent from tissue 1 6 Gain control in two dimensions for additional level of flexibility to image quali
65. raphic display NEM One yoke hanger each for Oxygen amp Nitrous Oxide Separate Pipeline inlet for Oxygen Nitrous Oxide and Air PT Hypoxic Guard to ensure minimum 25 O2 across all O2 N20O mixtures and Oxygen Failure Warning 10 jBreathing system PM Latex free fully autoclavable Flow sensing capability at inhalation and exhalation ports sensor connections shall be internal to help prevent 12 disconnect nB Sensor should not require daily maintenance Bag to vent switch shall be bi stable and automatically begins mechanical ventilation in the ventilator position E E E Cn 16 Should have adjustable pressure limiting valve breathing circuit pressure measuring device 17 Should have a bag ventilator selecting valve integrated onto the absorber 18 shoudbesutabletouselowtfiowtechnigues O O OCO SoS 19 peudhweibutoygensmso O 20 SheudhaveCO2absobentchambercamster O 1 eges 700000000000 New generation Vaporizer must be isolated from the gas flow in the off position and prevent the simultaneous 22 activation of more than one vaporizer Vaporizer should mount to a Selectatec manifold of 2 vaporizers which allows easy exchange between agents 23 Temperature pressure and flow compensated vaporizers and maintenance free for Isoflurane and Sevoflurane LE 4d 24 3 5 Integrated Ventilator oe The workstation should have integrated Anesthesia Ventilator system for adult and paediatric
66. round 550 mm 5 Foot part should be fixed Length around 1 400 mm 6 Should have 2 push handles chromed y 8 9 10 If the side guards are not used they should be able to stick in converse into the holders Length side guard should be around 700 mm Height over upholstery should be around 200 mm Should have central breaking system with steering facility and bumpers at all four corner Facility for fixing IV road and fixing accessories monitor Infusion pump etc Good Quality hygienic mattress with straps for fixing Place for keeping oxygen cylinder in the trolley Good quality SS collapsible side rail and I V Rod should be provided with the trolley po pP EU Should have 2 side guards stickable chromed DepartmentsINo OOO equipments e OOO BomedislAset No LL Qumy j 0 Smir ems SL NO SPECIFICATION a Mesmumlenghshoddbesround20SO21S0mm 2 jWeeWikhshoudbearound0800mm 3 HeghtshodbearoundS35 900mm O OC a endeenbergshoudbed degStepless OOOO O 7 OSS 5 Anti Trendelenberg should be 7 deg Stepes O OCS 6 heudheXRayPermesbleareaforemielengh O O OC l 7 Whedimetersheudbemiimumis mm O Should have facilities for fixing I V Rod and preferably a place for fixing accessories Monitor Infusion pump etc at head end e es oe Should have good qual
67. systems so Feiitytostoresnspshotsduringcri caleventsforwaveformreviewatalaterstage 40 jwiovsulandgrdedsrmmgsytem 41 oisplay of Ventiators 42 m vdume V OOO C f a inspiratory expiratoryratio i aa 45 Pressure ime Pim O OOOO 46 Positive End Expiratory Pressure PEEP O O O 47 eentrafized Monitoring and Networking Central Monitor with Ethernet Networking of all the OT Monitors with Laser Printer and with client computer in office of Doctor In charge for browsing real time waveforms graphical amp numerical trend up to 24 hrs from each 48 OT Monitor Facility to browse remotely using internet near real time waveforms and graphical amp numerical trend upto 24hrs optional WIEN a li 4 System Configuration Accessories spares and consumables 3 jAmestesaGasDelverysstem 0 O O OO S S 2 Circle absorber 01 TwinChamber SS SOS E 0 0L L 4 Menter 0d ooo wp Vaporizer Desflurane 01 optional wp 6 Vaporizer Sevoflurane 01 b Wed Vaporizer Isoflurane 01 1 8 Adult and Paediatric autoclavable silicone breathing circuits 02 each o fewsbeibcbledd SSCS 10 biposbelbPtansduersio O O 1 pemppobesinrewable 0 O
68. tleast 20 seconds of doppler and M mode data 7 igh frame rate review for better clarity of playback images study in slow motion 9 0 1 1 2 2 22 23 User defined system and application presets for multi user department The number of application presets is to be mentioned 2 2 2 2 4 In built hard disk storage capacity of atleast 80 GB with facility of direct storage and retrieval of B W and color images both frozen and cine loops CD DVD drive for read and write of stored images 7 5 6 Alpha numeric key board with illuminated keys and status display Key panel Height Adjustment Should be Possible All panel key should be customized including Freeze Key Facility for high definition digital acquisition review and editing for complete patient studies 31 3 Active Ports should be available Any Probes any Port interchangeable connectivity should be possible with simple electronic selection method for interchanging transducers Detailed Radiology obs amp gyn and vascular measurement packages should be available System should have extensive calculation packages a Distance volume Area 96 stenosis on B mode b Distance Time Heart Rate Slope on M mode c Velocity Acceleration time Slope PI RI S D Ratio with Auto Doppler calculation on Doppler mode systolic diastolic cardiac function and IMT Quantification Package Us 2 ee eee Enhancement settings The system should have gate a
69. ty control NEIGE Real time high frequency 2D for higher resolution and low frequency Doppler for higher sensitivity in all probes pr 8 Frame rate should be 500 FPS or more oo 0 9 Steerable PW CW on all phased array probes High definition acoustic zoom for enlarging sections of 2D and color flow images with more acoustic information for greater clarity and detail while maintaining an optimal frame rate simultaneous display of thumbnail views on the same system display monitor The system shall support display of all multiplanar views and the rendered image during 4D acquisition The system shall support volume measurements and analysis on quantitative 3D and 4D data The system shall support simultaneous display of volume and multiplanar MPR views Monitor should be High resolution non interlaced LCD Color monitor of 20 inches or more with tilt and swivel facility to view in all angles and all light conditions D nB Color flow imaging for PT Increased lateral amp spatial resolution E Detection of even subtle areas of turbulence displaying a more physiological blood flow appearance without loss of frame rate PE Color flow with capability of automatically picking up color flow as a function of focal depth Sa m Tissue colorization B Color for improved contrast resolution eo e Modes 2D 3D 4D B Mode B B Mode M Mode steerable PW CW Doppler color Doppler tissue doppler B M Mode B PW Doppler B CW Doppler
70. ut Common Mode rejection 90db at 50 60 Hz o Alarms Quickset ve Ams 30 men 000000000 i esuengRespomeA DagnoticOOSto1S0Rg O OOS S Monitor 06740 LL jePdes25to30 g pAmogtcGOuputoG7t032H 32 Defibrilator External Paddles 1 Nos and Disposable Paddles 10 Nos for hands off defibrillation Ememyseect2jouestoz01odes O OOOO S 38 low energy Biphasic Shock Advisory System O O OSOS 34 Protection against inappropriate delivery of shock O 35 ACandDCPowerAdaptor OO O OOS HEU VEDHER e HC ORG IIR E ME REN M GANE RN HC RE 3 TERMS AND CONDITIONS OF SUPPLY INSTALLATION AND COMMISSIONING 3 meseteifeshudbeatemtSyems O OC OCO O I EE Ni 5 3 The equipment should be guaranteed for a period of 2 Years after the successful Installation and Commissioning MENU Annual Maintenance Contract for 5 years after the period of Guarantee should be quoted along with the Tender PART B MEDICAL FURNITURES LoeprtmemsiNo EupmensiNo ps OOOO Biomedical Asset No OOS Quy po T Smhrtems SL NO SPECIFICATION 1 Technical Specifications d Should be 2 sectioned height adjustable stretcher trolley 5 Should have manual foot operated height adjustment by hydraulic pump Should have pedals for foot controlled height positioning are bothsides the table 3 4 Length of head part should be a
71. ystem shall be able to be connected to an optional footswitch for hands free operation hn me x B w Thermal Printer of latest model with CE or FDA mark ee UPS of appropriate rating with 60 mins back up additional to in built battery back up 4 POWERSUPPY 1 Power input to be 220 240 V AC 50 Hz 5 STANDARDS SAFETY AND TRAINING PT Should be FDA CE BIS approved product hn EE aa Manufacturer should have ISO certification for quality standards SENE On Site Comprehensive training for lab staff and support services till customer satisfaction with the system 6 DOCUMENTATION hm o a User manuals to be supplied in English Oooo ee ee Service manuals to be supplied in English Department SI No amp upmenSNo RB O OOOO Biomedical Asset Nox OOOO Quy o Smarten SCC SL NO SPECIFICATION 1 OPERATIONAL REQUIREMENTS Should should be latest generation state of the art portable color Doppler for abdominal vascular musculoskeletal small parts basic cardiac and nerve block application with suitable evaluation and measurement packages 2 TECHNICAL SPECIFICATION bo peces System should be offered with following electronic multi frequency Broad Band width transducers Convex array transducer frequency range of 2 to 6 mHz for general purpose abdominal gynecological and 2 Obstetric imaging BH linear array transducer 6 13 mHz for small parts vascular musculoskeletal nerve blocks and

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