Patliputra Medical College - Jharkhand
31419364 purchase machine instrument anaesthesia snmmc dhanbad purchase machine instrument anaesthesia snmmc dhanbad cooled radio frequency nerve ablation machine 1 the equipment should be useful for standard rf ablation & cooled rf ablation. 2 indications: cervical pain, thoracic pain, facet pain, lumber pain, sacro iliac joint pain, discogenic pain, hip joint pain, knee pain etc, 3 rf generator must support bipolar rf for biacuplasty procedure. 4 the rf machine must have separate quad cool pump assembly to treat cooled rf related muscle / nerve origin chronic pain pathology. 5 rf must have water cooled probe. 6 the equipment should have following features in a single unit: a ) standard rf, b ) pulsed mode, c ) cooled rf, d ) bipolar mode. 7 the system should have customizable treatment profiles for quick access. minimum 15 treatment profiles can be added and deleted as per user convenience. 8 the system should be able to record clinical logs for the past therapies. minimum 120 procedure logs should be supported. 9 the system should support individual probe control before and during treatment. start and stop function for individual probe with respect to temperature and time. 10 the system should automatically extend procedure time if set temp does not reach allotted ramp time. 11 the system should view display ramp time, time at set temp, and total procedure time in graph form. 12 the system should have demo mode for cooled, standard, bipolar, trandiscal, pulsed and stimulation mode for users to review.13 the system should be able to test pump unit, upgrade software and enable live output. 14 the system should display warning with numeric code and actionable error message. 15 screen display • the equipment should have lcd color touchscreen. • should display graphical interface in real time, display impendence, temperature, time and voltage independently. 16 rf energy: standard temperature & time duration: • for standard rf: temperature display 80 degree c and time 90seconds • for bipolar rf: temperature display 40 degree c and time 15 minute • for pulse rf : temperature display 42 degree c and time 90 seconds • for cooled rf: temperature display 60 degree c and time 2:30 minutes. 17 on insertion of rf cable, the equipment should recognize the • standard rf probes • bipolar probes for discogenic pain • cooled rf • should have automatic mode to recognize various cables for minimal manual operation. 18 impedance measurement, stimulation, rf output: • the impedance measurement should be in the range of 1 3000 ohms • impedance can be measured in before and during lesion in “lesion mode, before stimulation mode” and during cooled rf in auto temperature mode. • stimulation voltage mode: 0.00 10 v, 0.01 v increment• current mode: 0.00 10 ma, 0.01 ma increment. • stimulation rate: 1 shot, 2, 5, 10, 20, 50, 75, 100, 150, 180 and 200 hz• stimulation pulse duration: 0.1, 0.2, 0.5 and 1.0 ms• rf energy: 460 khz• maximum power: 80w 19 software shutdown limits during rf delivery or stimulation ( safety features ) : • measured impedance: < 25 o or > 3, 000 o • measured temperature: < 15°c, > 100°c. 20. certification / standards of equipment’s: • the system should have csdco registration in india for assuring trusted supply of consumables. • the equipment must be iso, european ce / usfda approved. • equipment must have supporting clinical papers and trials performed on the machine with outcome of the clinical trials. • operational manual should be provided with the equipment. 21 scope of supply: :a ) r. f. machine ( advanced cooled upgradable generator ) : 1 no, b ) connecter cable for trans discal biacuplasty procedure: 1 no. c ) 4 channel standard rf : 1 no. d ) 4 channel cooled rf 1 no. e ) peristaltic quad pump to perform multi cooled rf. this needs to be operated in conjunction to the rf generator.: 1 no 22 the equipment is to be supplied with consumables: • rf split grounding pad : 10 nos. • standard rf flexible probe 100mm length, reusable : 1 no. • standard rf flexible probe 145mm length, reusable: 1 no. • standard rf cannula supporting 100mm length, 5 mm active tip: 10 nos. • standard rf cannula supporting 100mm length, 10 mm active tip: 10 nos. • standard rf cannula supporting 145 mm length, 5 mm active tip : 10 nos. • standard rf cannula supporting 145 mm length, 10 mm active tip: 10 nos. • knee procedure cooled rf kit 75mm probe length, with 4mm active tip : 1 no. • lumber facet / si procedure cooled rf kit 150 mm probe length, with 4mm active tip: 1no. • hip joint procedure cooled rf kit 100 mm probe length, with 4mm active tip : 1 no. 23 demonstration before purchase: for technical evaluation, if required demonstration of the machine should be arranged at the cost of the company. 24 terms & conditions: warranty / cmc • after installation of equipment, the supplier / manufacturing company shall provide free warranty for 3 years. • the supplier / manufacturer should make available spares & consumables of rf machine for the life as per tender. • parent company should provide undertaking of suppling the probes and cannula for 10 years from the date of installation of machine. • parent company should not increase the prices of probes and cannula more than 10 % each year. • parent company should give written agreement to supply the standby machine within 5 working days in case of any problem or issue with the machine installed in the hospital. 25 • parent company should have registered office in india. • product should have atleast 5 yrs. of market standing in india. predicate product having same application is valid under this scope of requirement. • in relation to the quoted machine, please attach users list of india. 26 training and support: • parent company should provide technical training support to the user department. • the parent company shall provide training in india at cost of the company on regular interval to at least two deputed staff members of the department. • the training is to be arranged at reputed government training center or at the centre where machine is being used for pain relief procedures. • the training accommodation & to & from travel cost expenditure is to be at the supplier / parent company end. • during initial period & after training, the company should provide authorized person to assist the staff of dept. in using the machine for the rf procedures / cases as & when required. • service engineer should be available with the authorize distributor end. , fluoroscopy machine ( c arm ) it should have: microprocessor controlled generator with 15” or more touch screen control panel for all operative parpanesh selection, live image and messages of eventual fault conditions. self diagnostic program on startup and display of self diagnostic maintenance. monitoring of mamin and mamax , x ray tube head max temperature, max kv, min kv and display of error message on lcd screen x ray generator type : high frequency x ray generator single tank. output power : 2.2 kw or more x ray tube: tube type : dual focus, rotating anode x ray tube.image processing: should have digital image memory pc based with storage ofmore than 10000 images in 1024x1024 format. c arm mobile stand: c arm stand should be sturdy, vibration free; self balanced and should have easy maneuverability. flat panel detector: flat panel detector : flat panel detector, amorphous silicon, csi:ti pixel area: 20cm x20cm or better, monitors: 32” high resolution, flicker free flat screen monitor with split screen display of live image / last image hold orsaved memory image mounted on modular design mobile trolley having caster wheels & locking system. accessories: a. lead apron 5nos. ( light weight, zero lead ) b. thyroid shields 5 nos ( light weight, zero lead ) c. lead gloves – 10 pairs ( single use type ) d. lead goggles – 02 nos e. lead apron mobile stand with hangers for lead aprons – 01 no ( note that lead apron and thyroid shield must be of reputed brand, should be usfda or european ce certified, copy of certificates as stated need to be submits in technical bid. ) important conditions a. must have valid aerb type approval certificate and bis certificate or equivalent iec. b. must be european ce certified from 4 digit notified bodyor usfda approved. c. should be iso 9001, iso 13485 and icmed 13485 certified. d. should be operable on 220 240vac, 50hz , patient controlled analgesia system for regional anaesthesia ? flow rate range 0.01 999.9ml / h. ? 0.01 99.99ml / h in increments of 0.01ml / h. ? 100.0 999.9ml / h in increments of 0.1ml / h. ? syringe sizes: 2 / 3; 5; 10; 20; 30; 50 / 50ml. ? online rate modification without delivery interruption. ? accuracy offset delivery rate equal or less than typ.+ / 2 %. ? bolus application delivery rate 1 – 1, 800 ml / h; max. bolus volume 99.99ml. ? bolus on demand. ? bolus with volume / dose pre selection. ? bolus over time ( 1 min 24h ) . ? occlusion pressure: 75 mmhg to 900 mmhg. ? kvo rate. ? rate >= 10 ml / h: kvo rate 3ml / h ? rate < 10 ml / h: kvo rate 1ml / h . ? rate < 1 ml / h: kvo rate = set rate. ? user individual configuration or deactivation of kvo rates possible. ? drug library: 750 drugs including all parameters in drug library up to 10 user defined drug categories. ? medication error prevention through dose limits referring to selected drug. ? automated syringe change for optimal start up characteristics. ? standardized user interface for all syringe & volumetric infusion pumps. ? optional upgrade of pumps to special therapy like tci, pca of the same ? integrated docking system with central alarm and running indication dose calculation automatic calculation of the delivery rate based on dose entries in mg, ?g, ie or mmol, weight and / or time related ( e.g. mg per kg / min; mg / kg / h; mg / kg / 24h, bolus application in mg, ?g, ie, mmol per kg and / or per time unit ( min ) with automatic calculation of the bolus rate for one bolus infusion. key pad: clearly structured, back lit key pad with not more than 8 keys for fast and intuitive operation; identical to infusion pump. safety features: free flow protection: integrated piston brake within syringe drive to prevent free flow during syringe change. occlusion alarm pressure limits: adjustable in 9 steps ( 0.1 1.2 bar or display in mmhg ) data lock: adjustable in 2 safety levels ( parameters and disposables ) automatic bolus reduction after occlusion alarm power supply: main power supply: mains adaptor ( rated voltage 100…240 v ac, 50 / 60 hz ) for standalone operation. external low voltage: 11 … 15 v; via external power supply 12 v or via central power station battery type: rechargeable nimh battery pack, quick and easy exchange without using screw driver to open the pump. battery operating time approx. 14 h at 20 ml / h with battery capacity display in h and min. pca pump should be usfda & ce certified. , styleted epidural catheter , rac’s catheter , intrathecal infusion pumpspump and catheter part of an implantable, programmable drug infusion system that store and deliver medication into the intrathecal space. combined with the control, to eliminate systemic opioids and provide effective pain relief. smart software to guide the clinician through programming the system, via information and warning screens full body mri compatibility at 1.5 and 3 tesla under specific conditions. critical therapy and patient data stored in the pump for follow up at other institutions. flex dosing schedules should allow drug delivery to be matched to patient needs, providing chronic pain relief throughout the day should have a separate touchscreen interface compatible with the pump. should have simple steps for refill and implant. built in auto calculations for volume and rates. software for patients who can alleviate their unpredictable pain without the use of systemic opioids. one can set a therapeutic daily dose and allow patients on demand bolusing within limits. feature of clear and informative bolus confirmations, lockout details, and alerts. should be easy and simple to use. , pain assesment chart , ot table ( fluoroscopy compatible ) four section eccentrically positioned radio translucent table top without cross members to facilitate c arm imaging. the table top made of radio translucent material for excellent fluoroscopic capability. operating positions i.e. height adjustment, trendelenburg, reverse trendelenburg, lateral tilt and back section precisely controlled by handheld remote.the powered movements actuated by electro hydraulic system comprising of hydraulic motor pump with low noise level of less than 50dba and solenoid valves to assure smooth and quiet movements. the head and leg section removable and interchangeable, capacitating a single table’s use in varied surgical procedures. these are manually operated by means of ratchet system.built in kidney elevator – manually gear operated. non corrosive ss304 grade stainless steel base and cylinder covers, side rails, clamps and standard accessories. table top size ( l x w ) : 1900 x 500 mm height : 750 mm 1000 mm trendelenburg / reverse trendelenburg :min ± 20° lateral tilt ( left / right ) : min. ±15°back section adjustment : + 80° – 20° down leg section adjustment : + 15° – 90° head section adjustment : +45° – 90° down, variation ±10%load capacity : 180 kgspower supply : 220v ac – 50hzwith orthopaedic attachments , anodyne machine ( for diabetic foot care ) designed to provide foot and leg pain relief by increasing foot and calf circulation. the pain relief technology should deliver two 30 minute treatments in between a 20 minute cooling cycle and has an auto shut off feature that activate after each 80 minute session. should have comfortable foot and calf therapy pads to increase circulation over a total therapeutic surface area , transcutaneous electric nerve stimulating machineshould be non invasive radio frequency pain management using neuro modulation portable battery operated small sized unit should be useful for treatment of: chronic pain relief, neuropathic pain & symptoms, diabetic neuropathies, bell’s palsy, trigeminal neuralgia, tennis elbow, golfer’s elbow & regional pain syndromes. square wave output with a superimposed rf waveform graphical display with backlight output current range of 0 30 ma transcutaneous nerve mapping with nerve mapper probe on board timer to keep track of therapy time user adjustable pulse width 0.1 ms and 0.2 ms user adjustable frequency of 1, 2, 5, 10 hz must have iso 13485 and ce mark. , anaesthetic machine with resuscitation equipment anaesthesia delivery machines ( boyle’s apparatus ) should be suitable for trauma, minor operating rooms adult and paediatric applications facility and connections for 2 gases: oxygen and nitrous oxide. the machines should have the facility for low flow anaesthesia procedure with the placement of 4 tube rotameters / flowmeters. anti hypoxia guard that ensures a minimum of 25% oxygen supply. nitours oxide cut off system. ofwd alarm system in case of oxygen failure. low battery alarm. high / low pressure alarm connection of a selectatec bracket back bar to mount tec. vaporisers should be supplied with vaporiser. connection of pin index cylinders and pipeline connections for supply of gases. ms metal frame + frp fibre body. , monitors with vital signs ( nibp, pr, ecg, spo2, temp, rr ) 1. should be suitable for monitoring of nibp, pr, ecg, spo2, dual temperature and rr of adult, paediatric neonatal patients. should have monitoring, surgery and diagnostic modes. 2. should have defib and esu protection, st analysis, arrhythmia detection, pacer spike detection, drug dose calculation and oxycrg as standard in every monitor. should have advance arrhythmia monitoring for asystole, vfib / vtac, vt>2, couplet, bigeminy, trigeminy, r on t, pvc, tachy, brady, missed beats, irr, pnc, vbrady. 3. should have integrated 12’’ or above tft lcd colour touch screen display with minimum 8 channels of waveforms 4. trend and events with waveform as standard, 48 hours full disclosure. 5. nurse call, vga output port should be standard. monitor should have usb port for software upgrade. should have inbuilt three channel recorder as standard in every monitor. 6. should have 350 min or more of battery backup as standard. wired and wireless networking should be standard to connect to central station. 7. anti theft lock facility should be possible for better hospital asset management. 8. should be ud fda or european ce complying to european directive 93 / 42 / eec for both monitor and software to control physiologic monitoring systems. 9. scope of supply must include: • basic unit with ecg, spo2, dual temp, nibp, inbuilt battery, inbuilt three channel recorder – 1 no • 5 lead ecg cable – 1 no each per monitor • ecg disposable electrodes – 30 nos per monitor • spo2 finger sensor – 1 no per monitor • skin temperature probe – 1 no per monitor • core temperature probe – 1 no per monitor • nibp hose – 1 no per monitor • adult & paediatric cuff – 1 no each per monitor • paper rolls – 4 no per monitor , central venous line catheter double lumen double lumen central venous catheter 7f ( 16g / 16g ) , made of certon, a special grade polyurethane, length 15 / 20cm, 18g valve needle having side port, novlon material dilator, scalpel, nittinol guidewire, safesite connector and ecg lead. , central venous line catheter triple lumen triple lumen central venous catheter 7f ( 16g / 18g / 18g ) , made of certon, a polyurethane, length 15 / 20 cm, 18g valve needle having side port, novlon material dilator, scalpel, nitinol guideeire, safesite connector and ecg lead , spinal epidural setcontinuous epidural anesthesia kit 18g with lor, filter and 3 pair of catheter opening latex free continuous epidural anesthesia kit containing g18 / g16 epidural touhy needle with large crystal clear grooved transparent hub & epidural catheter of g20 / g 19 & length 100 cm. with catheter connector. epidural catheter in the kit made of 2 layers inner layer of polyamide & outer layer of polyurethane. epidural catheter should have an atraumatic tip design a tapering tip upto 4 cm & 3 pairs of laser drilled holes for distribution of drug, also a small compact ergonomic 0.2 micron epidural filter with pressure resistance of 7 bars, 10ml loss of resistance syringe with leur slip and parabolic graduation markings. , spinal epidural set combinedspinal epidural catheter set with back eye touhy needle. latex free disposable pencil point spinal needle 27g, 127.5 mm with grooved transparent hub with centering protective plastic sleeve, touhy needle with black eye 18g ( 1.3 x 88 mm ) . protrusion of spinal needle through the back eye of the epidural back eye of the epidural needle. with epidural catheter, filter, loss of resistance syringe and separate locking device – docking system. , epidural needle 18g , crash cart• made of crca pipe / sheet. • six drawer of two different sizes. • mounted on 125 mm castor, two with breaks. • accessories: defib stand, oxygen cylinder, iv rod, 2 dustbin, extension cord, six coloured pvc bins, cardiac massage board. • one drawer with pvc drug holders. , suction machinea sturdy suction unit for major surgical procedures including neuro surgery, orthopaedic surgery where the blood loss is more than usual. 2 ( psu ) jars of 4 ltrs. mounted which should be autoclavable. 600mmhg, 60ltr. per minute. electronic sensor. , baby warmeromicro processor controlled infant warming system. o should have four mode of operation: servo skin, safe, pre warm and manual. o the baby bed should be tiltable at both sides for trendelenburg and fowler’s position. o should have an inbuilt cabinet. o touch operation with large digital display. o thermistor based temperature sensor. ocomprehensive alarms. o should have sense technology to detect the detachment of skin probe and should decrease the temperature gradually to protect the baby from hyperthermia o memory backup to restore set temperature and control mode automatically, in the event of power failure. o apgar timer up to 1 59 minutes. o the heater module should easily pivots 90 degrees in either direction to facilitate other procedures like x rays without disturbing the baby. o optional features to upgrade – electrical height adjustment, in built weighing scale, oxygen cylinder mounting provision, flow meter, x ray cassette tray o certification: qms – iso 13485, ce o should have safety test reports. , instrument boiler big size• electric instrument sterilizer & boiler • stainless steel construction. • fitted with thermostat & tray lifting arrangement • size: 18 x 8 x 8 inches , ot table ( electronic ) • electro mechanical driving mechanism with smooth and quiet movements. • table top should be made of radio translucent material for fluoroscopic capability. • operating positions including height adjustment, trendelenberg, reverse trendelenberg, lateral tilt and back section can be controlled quickly and accurately with the help of a lightweight hand control unit. • interchangeable head & leg sections and manually operated by the means of precise ratchet system. • the eccentrically positioned table top, without cross members, to optimize image intensifier accessibility for both a / p & lateral exposures. • base and column covers made of stainless steel for easy cleaning and hygiene. elevation range lowest / highest 735mm / 1035mm. trend. / rev. trend head up / down 25° lateral tilt left / right 20° back section up / down 70° / 30° flex & reflex220° / 100° leg section ( manual ) up / down 15° / 90° head section ( manual ) up / down 40° / 90° accessories: l shaped anaesthetic frame: 1 pc. shoulder support with pad: 1 pair. arm board with s.s top: 2 pcs. lateral support with pad: 1 pair. wrist strap: 1 pair. knee crutches goepal type: 1 pair. waterproof rubber mattress: 1 set , autoclave machine ( 2drum ) double drum autoclave, these steam sterilizers should be designed to accommodate dressing drums of size 15 x 12 inch ( dia. x length ) . , ot ceiling light ( led ) ( a ) double dome operating light must be designed for the use in high demanding surgical procedures. state of the art led bulbs should be used to ensure a low energy consumption and a long service life. ( b ) outer handles at the light head should be provided to allow for non sterile positioning. ( c ) light head must be designed with smooth transitions and surfaces, without slots, gaps or exposed screwing to ensure fast and effective cleaning. ( d ) the light head must be resistant to disinfectant. ( e ) for sterile positioning an ergonomic, exchangeable and centrally positioned sterile handle within the light head should be provided. ( f ) all main joints of surgical light must be provided with unlimited rotation ( 360° ) . light head and suspension must be sealed dustproof. ( g ) control of illumination intensity must be possible via wall control panel ( h ) the surgical light should be complete with all components for ceiling mount and electrical feed in, incl. finalised installation. ( i ) certification – should be us fda approved. ( j ) warranty: 3 years. ( k ) technical data of main dome:i. central illumination intensity ec 160.000 lux ii. light field diameter at a distance of 1 m 200 mm iii. depth of illumination l1+l2 1300 mm iv. average color rendering index ra 95 v. color rendering index r9 ( red ) 93vi. color temperature 5000k vii. central illumination at 1m distance with: • tube 100% • one mask: 40% • tube and one mask: 40% • two masks: 48% • tube and two masks: 48% viii. central irradiance ee 580 w / m² ± 50 w / m² ix. ee / ec ratio 3.5 w / m2 x lux x. adjusting the illumination intensity 40000 to 160000 lux xi. number of led 66 units xii. number of led stripes 11 units xiii. service life led bulbs approx. 30000 hours xiv. replacement of led bulbs – should be possible xv. ambient light mode ( endolight ) 300 lux xvi. diameter of light head – approx. 600 mm. ( l ) technical data for satellite dome 1nos. xvii.central illumination intensity ec 120.000 lux xviii. light field diameter 200mm xix. depth of illumination l1+l2 1300 mmxx.average color rendering index ra 95 xxi.color rendering index r9 ( red ) 93xxii. color temperature 5000k xxiii. central illumination at 1m distance with a. tube 100% b. one mask: 41%c.tube and one mask: 41%d. two masks: 49%e. tube and two masks: 49% xxiv. central irradiance ee 430 w / m2 ± 50 w / m2 . xxv. ee / ec ratio 3.5 w / m2 x lux . xxvi. adjusting the illumination intensity 40000 to 120000 lux. xxvii. number of led 48 units . xxviii. number of led stripes 8 units. xxix. replacement of led bulbs possible. xxx. service life led bulbs approx. 30000 hours. xxxi. ambient light mode ( endolight ) 300 lux. xxxii. diameter of light head 620 mm , ot led light ( mobile ) ( a ) single dome operating light must be designed for the use in high demanding surgical procedures. state of the art led bulbs should be used to ensure a low energy consumption and a long service life. ( b ) outer handles at the light head should be provided to allow for non sterile positioning. ( c ) light head must be designed with smooth transitions and surfaces, without slots, gaps or exposed screwing to ensure fast and effective cleaning. ( d ) the light head must be resistant to disinfectant. ( e ) for sterile positioning an ergonomic, exchangeable and centrally positioned sterile handle within the light head should be provided. ( f ) all main joints of surgical light must be provided with unlimited rotation ( 360° ) . light head and suspension must be sealed dustproof. ( g ) light should be mounted on a rigid stand with hardy wheels, so that can be moved easily within hospital. ( h ) the surgical light should be complete with all components for mobile use. ( i ) certification – should be us fda approved. ( j ) warranty: 3 years. ( k ) technical data: i.central illumination intensity ec 120.000 lux . ii. light field diameter 200mm. iii. depth of illumination l1+l2 1300 mm. iv. average color rendering index ra 95. v. color rendering index r9 ( red ) 93.vi. color temperature 5000k. vii. central illumination at 1m distance with: a. tube 100% b. one mask: 41%c.tube and one mask: 41% d. two masks: 49%e. tube and two masks: 49% viii. central irradiance ee 430 w / m2 ± 50 w / m2. ix. ee / ec ratio 3.5 w / m2 x lux.x. adjusting the illumination intensity 40000 to 120000 lux xi. number of led 48 units. xii. number of led stripes 8 units. xiii. replacement of led bulbs – should be possible. xiv. service life led bulbs approx. 30000 hours. xv. ambient light mode ( endolight ) 300 lux. xvi. diameter of light head – approx. 600 mm , high pressure steriliser electric horizontal chamber size 600x1100mm sterilization temp. range 99 to 121ºc sterilization pressure range max. 1.2 kg / cm² standard lid lock mechanism: radial lock stainless steel grade ss304 triple walled design with mineral wool insulation for prevention of burn to users. , cautery machinepower output: maximum cut power ( vio 300 s ) 300 watts at 500 ohm ( with pps, briefly 400 watts ) maximum cut power ( vio 200 s ) 200 watts at 500 ohm maximum coag power up to 200 watts ne safety system nessy frequency 350 khz power connection : line voltage 100 v – 120 v / 220 v – 240 v ± 10 % power frequency 50 / 60 hz line current max. 8 a / 4 a power consumption in standby mode 40 watts power consumption at max. hf power 500 watts / 920 va potential equalization connection yes power fuse t 8 a / t 4 a us fda or european ce , syringe pump the syringe pump should be programmable, user friendly, should have battery backup and comprehensive alarm system. flow rate range: 0, 01 999, 9 ml / h, 0, 01 999, 9 ml / h in 0, 01 ml / h steps, calculation of the rate by selecting the time & volume. rate change without flow interruption. automatic detection of syringe sizes and flexibility of syringe sizes from 2 / 3 ml, 5 ml, 10 ml, 20 ml, 30 ml, 50 / 60 ml. volume pre selection: 0, 10 9999 ml in 0, 01 ml steps time pre selection: 00h01min – 99h59min total reset of infused volume possible without flowinterruption residual volume be available with single key pressdosage calculation: suitable for tiva applications. automatic calculation of the flow rate on the basis of dosage units in mg, ?g, ng, iu, mmol or meq time based and optionally weight based ( e.g. mg / kg / min; mg / kg / h; mg / kg / 24h ) . surface related calculation ( dubois ) bolus rate: • 1 1800 ml / h in 0, 01 ml / h steps standby possible • standby time adjustable from 1 min to 24 hours in 1 min steps integrated drug library: up to 3000 drugs can be utilized in the pump. pressure adjustable in 9 levels from about 0.1 bar – 1.2 bar key / function lock battery operation: battery capacity at 5 ml / h flow accuracy typically + / 2% including disposables acc. iec 60601 2 / 24 semi automatic drive three infusion pumps without additional accessories stackable and lockable fluid ingress protection , advance multipara monitor with bis and cardiac output1. should be suitable for monitoring of ecg, nibp, spo2, dual temperature, triple ibp, capnography, cardiac output and bis monitoring of adult, paediatric neonatal patients. should have monitoring, surgery and diagnostic modes. 2. should have defib and esu protection, st analysis, arrhythmia detection, pacer spike detection, drug dose calculation and oxycrg as standard in every monitor. should have advance arrhythmia monitoring for asystole, vfib / vtac, vt>2, couplet, bigeminy, trigeminy, r on t, pvc, tachy, brady, missed beats, irr, pnc, vbrady. 3. should have integrated 15’’ or above tft lcd colour touch screen displaywith minimum 10 channels of waveforms. 4. trend and events with waveform as standard, 48 hours full disclosure. 5. nurse call, vga output port should be standard. monitor should have usb port for software upgrade. should have inbuilt three channel recorder as standard in every monitor. 6. should have 120 min or more of battery backup as standard in every monitor. wired and wireless networking should be standard to connect to central station. 7. anti theft lock facility should be possible for better hospital asset management. 8. should be us fda or european ce complying to european directive 93 / 42 / eec for both monitor and software to control physiologic monitoring systems. 9. scope of supply must include: basic unit with ecg, spo2, dual temp, nibp, three ibp, etco2 monitoring, cardiac output, bis monitoring, inbuilt battery, inbuilt three channel recorder – 1 no • 5 lead ecg cable – 1 no each per monitor • ecg disposable electrodes – 30 nos per monitor • spo2 finger sensor – 1 no per monitor • skin temperature probe – 1 no per monitor • core temperature probe – 1 no per monitor • nibp hose – 1 no per monitor • adult & paediatric cuff – 1 no each per monitor • etco2 sensor with cable – 1 no per monitor • disposable bis sensors – 25 nos per monitor • accessories for co – 1 no set per monitor • paper rolls – 4 no per monitor , automated external defibrillatorit should be light weight portable biphasic automated external defibrillator with easy to use interface and user friendly audio and visual prompts. it should automatically analyze the patient’s ecg and has a metronome signal tone to synchronize chest compressions. it should have following features: current controlled biphasic wave form. •programmable energy level pattern for first 3 shocks. •up to 200 shocks with a new battery. •visual an audible scan indicator. •regular selftests to evaluate device condition. •continuous voice to aid revival. •disposable self sticking electrodes. •regular monitoring of battery levels. •metronome signal fo synchronizing chest compression. •should have sd card facility for data transfer. •two energy levels energy level low ( 150j ) and high ( 200j ) ( in aed, highest energy level is 200 joules ) . •in addition to color coding and alarms, it should come with one touch operation making the usage simple and convenient. •should have european ce / usfda certification. •indian subsidiaries and dealers should have nation wise network & local support. , amc % , cmc %...