Supply And Installation Of Picu/Nicu Equipments For Igh Kavaratti Supply , Installation , Commissioning , Provide 3 Years Comprehensive Warranty And 5 Years Camc After Expiry Of Warranty Period For The Picu/Nicu Equipments For Igh Kavaratti, Lakshadweep-Lakshadweep

TDR : 28428891

Tender Notice
Corrigendum Details
BOQ

Expired

Lakshadweep , Lakshadweep

Tender Brief : Corrigendum : Supply And Installation Of Picu/Nicu Equipments For Igh Kavaratti Supply , Installation , Commissioning , Provide 3 Years Comprehensive Warranty And 5 Years Camc After Expiry Of Warranty Period For The Picu/Nicu Equipments For Igh Kavaratti

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Submission Date
29-07-2021

Competition Type
Indian

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Sr No	Corrigendum Date	Corrigendum	Type	New Submission Date
1	28-07-2021	Date Extension	Date	03-08-2021
2	28-07-2021	Updated BOQ (installation of PICU/NICU equipments for IGH,Kavaratti)	Other	29-07-2021

Name of Work:Supply, Installation,Commissioning provide 3 year comprehensive warrenty and 5 year CAMC after expiry of Warranty period for the PICU/NICU Equipments for IGH,Kavaratti
	Sl.No.	Name of Goods	Item Code / Make	Quantity as per Tender	Units
1	1	Syringe pump \nTechnical Specifications\n1. Should be easy to use and nurse friendly	item1	3	Nos
2	2	2. Should have automatic syringe size and model detection
3	3	3. Should have large format LCD/TFT display.
4	4	4. Should have a minimum flow rate range from 0.1 – 1200 ml/hr for 50ml syringe, 0.1 -100 ml/hr for 20ml syringe and 0.1 – 60 ml/hr for 10ml syringe.
5	5	5. Syringe range from 20-50/60 ml.
6	6	6. Should have a flow rate accuracy of ±2%
7	7	7. Should have a bolus rate up to 1000ml/hr for 50 ml syringe.
8	8	8. Should have automatic and manual bolus.
9	9	9. Should have at least 3 levels of programmable occlusion pressure.
10	10	10. Should have automatic bolus reduction system to avoid accidental bolus delivery afterocclusion incident.
11	11	11. Should have a rechargeable battery with back up time of minimum 3 hours.
12	12	12. Pump must trigger following alarms with visual indication:-\ni. Occlusion Pressure Alarm \nii. KVO or 3 min pre- alarm \niii. Syringe empty and volume infused alarm \niv. Internal malfunction and Battery Charge Low Alarm \nv. Syringe disengaged and incorrectly placed alarm \nvi. Alarm loudness control. \nvii. No mains \nviii. Line disconnected (rapid pressure drop). \n
13	13	13. Should work with input 200 to 240Vac 50 Hz supply.
14	14	14. Should have safety certificate from a competent authority CE / FDA (US) / STQC CBcertificate / STQC S certificate or valid detailed electrical and functional safety test report from ERTL. Copy of the certificate / test report shall be produced along with the technical bid
15	15	Infusion pump\nSpecification\n1. The syringe pump should be programmable, user friendly, safe to use and should have battery backup and comprehensive alarm system.	item15	2	Nos
16	16	2. Must Work on commonly available standard 5ml/10ml/20ml/50ml/60 ml Syringes with accuracy of minimum of +/-2% or better, with automatic syringe size recognition.
17	17	3. Manufacturer should be ISO and European CE certified for quality standards.
18	18	4. Flow rate programmable from 0.1 to 1000 ml/hr or more in steps of 0.1 ml/hr with user selectable flow set rate option. SAVE last infusion rate even when the AC power is switched OFF.
19	19	5. Bolus rate should be programmable to 40 to 1000 ml/hr or more with infused volume display and one key press bolus, auto bolus as a advance feature with programmable bolous rate.
20	20	6. Display of Drug directory of more than 50 drugs, customized and adjustable.
21	21	7. Key board locking system for patient safety.
22	22	8. 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.
23	23	9. Selectable Occlusion pressure trigger levels selectable from 300/500/900 mmHg.
24	24	10. Automatic detection of syringe size & proper fixing. Must provide alarm for wrong loading of syringe such as flanges out of slot; disengaged plunger, unsecured barrel etc.
25	25	11. Manual pusher with plunger protection guard.
26	26	12. Anti-bolus system to reduce pressure on sudden release of occlusion.
27	27	13. Should have comprehensive ALARM package including: Occlusion limit exceed alarm. Near end of infusion pre-alarm & alarm, Volume limit prealarm& alarm, KVO rate flow, Low battery prealarm and alarm, AC power failure, Drive disengaged and preventive maintenance.
28	28	14. Rechargeable Battery having at least 8 hours backup for about 5ml/hr flow rate with 50ml syringes. Larger battery life and indication of residual life will be preferred.
29	29	15. 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.
30	30	16. The unit shall be capable of stored and operating continuously in ambient temperature of 10 - 50deg C and relative humidity of 15- 90% .
31	31	17. Power input to be 220-240VAC, 50Hz.
32	32	18. User Manual and service manual in English.
33	33	Double surface LED phototherapy \nSpecification\n1. Should last for at least 30,000 hours	item33	2	Nos
34	34	2. Should be made of easily cleanable material
35	35	3. Minimum irradiance should be 20 µW/cm2/nm at 45cm distance between bed and light unit
36	36	4. Wave length should be 450-460 nm and should be free from UV and IR radiation
37	37	5. Should have visual and audible alarms for the following -\n• Internal temperature >550C\n• If cooling fan fails\n• If LED current increases or decrease\n• If LED volt increases or decreases
38	38	6. Cooling fan to be provided to dissipate the heat created by LED
39	39	7. Should be compact to use along with the radiant warmer and should have tilting facility so that unit is not coming directly under warmer
40	40	8. Smooth height adjustment mechanism & adjustable height
41	41	9. Peak spectral irradiance: at least 30 µW/cm²/nm at 30 cm distance and 50 µW/cm²/nm at 20 cm distance (as measured with Minolta-Airshields or Olympic flux meter)
42	42	10. It should be possible to increase or decrease the irradiance by a switch without changing the distance to the baby
43	43	11. Large effective surface area: mean spectral irradiance of at least 20 µW/cm²/nm over an area of 25cm by 50cm at 30cm distance
44	44	12. Emissions spectrum: blue light with a peak wavelength between 440 and 470 nm
45	45	13. The source of lamps (manufacturer) should be identified and acertificate of the emission spectrum from a government/research laboratory should be provided.
46	46	14. Quality control: device is produced by manufacturer with ISO 9001 certification (certificates to be submitted)
47	47	15. Electrical: device is compatible with 220 -240 V50/60 Hz power input
48	48	16. Durability: LEDs are protected by suitable cover made of fire-resistant transparent material
49	49	17. Digital Lamp time counter
50	50	18. Digital Treatment time counter
51	51	19. LEDs are protected by suitable cover made of fire-resistant transparent material
52	52	20. Sturdy mobile stand
53	53	21. At least 2-inch sturdy Castors, at least 2 should have breaks
54	54	22. Height of stand’s base must be less than 8cm to fit under radiant warmers/incubators and baby cots
55	55	23. Height adjustable from 1.20m to 1.50 m (measured from bottom surface of enclosure to ground)\ni. Light enclosure must be tiltable from horizontal to at least 30 degrees\nii. tiltable from horizontal to at least 30 degrees
56	56	24. The base of the unit should be such that it will go beneath any incubator/ bed/ trolley with minimum of 100 mm floor clearance.
57	57	25. 1 spare set of fuses per machine\n1. All the material /equipment should be European CE & US FDA. \n2. All the Electronic equipment’s should comply with Electrical safety conforms to standards for electrical safety IEC 60601-1.\n3. All the equipment’s power input should be 220- 240V AC, 50Hz fitted with Indian plug.
58	58	Multipara Monitor with paediatric and neonatal BP cuff \nSpecification\nGeneral:\n• Parameters – ECG, heart rate, respiratory rate, SpO2, NIBP, Dual IBP, EtCO2, Dual Temperature.\n• Should be Modular and capable of being connected to a central station.\n\n\n\n\n\n	item58	2	Nos
59	59	• The equipment should come with all standard accessories \nrequired to run all parameters.
60	60	• Waveform display: at least 12 channels at a time, user selectable.
61	61	• Digital display: Heart rate, respiratory rate, oxygen saturation,\n temperature, Blood Pressure (systolic, diastolic, mean).
62	62	• System should be compatible with HIS.
63	63	• System should be US FDA & European CE approved for \nquality assurance.
64	64	• Monitor must be able to connect to central monitoring station and \nshould use single network for all kind of networking with the central station or other hospital information system (HIS). It should have dual display, one for continuous display of all beds and other for trend review, full disclosure etc.
65	65	Individual Monitors:\n• Wall-mountable and pivotable.\n* Medical grade, TFT Flast screen,, slim size, at least 19\" display\n• Flexible display mode for various monitoring needs.\n• Should be knob control and touch screen.\n• Viewing angle at least 90o.\n• Bigger font of numeric should also be available.\n• Should have standby mode for temporary leaving of patients.\n• Adjustable contrast and brightness.
66	66	Should have facility to record data for individual patients identifiable by their name and hospital registration number\nThe following modules complete with their accessories for each monitor:\n• Heart rate\n• ECG\n• Respiration\n• Oxygen saturation\n• Temperature: 2 ports\n• Non-invasive Blood pressure\n• Invasive blood pressure 2 ports\n• EtCO2\n
67	67	The following modules are also required in the quantity mentioned\nParameters monitored: Cost of following modules should be quoted separately.\n• EEG – 2\n• NMT – 1\n• Minimal invasive Cardiac Output monitor – 2\n• BIS - 1\n
68	68	3. Heart rate/ECG:\n• 10-lead selectable ECG\n• Built in arrhythmia monitoring in all leads\n• Inbuilt ST segment analysis and arrhythmia detection facility\n• Display of 2 ECG leads simultaneously at a time\n• Heart rate range 20-250 bpm\n• Accuracy ± 5 bpm\n• Display sweep speeds 12.5, 25 mm/sec (user adjustable)\n• Averaging time: user selectable up to 8 seconds\n• ECG amplitude user adjustable\n• Defibrillator protected\n\n\n
69	69	4. Respiratory rate\n• Measured by transthoracic impedance using the same ECG lead\n• Range 0 to 150 breaths/min\n• Accuracy ± 2 bpm\n• Display sweep speeds 6.25, 12.5 & 25 mm/sec (user adjustable)\n• Averaging time: user selectable up to 8 seconds\n• User selectable apnea alarm time\n\n
70	70	5. Oxygen Saturation\n• Masimo-SET/FAST Technology to take care of low perfusion states and motion artifacts\n• Dual wavelength LED pulse oximetry\n• Range 1 to100%\n• SpO2 accuracy : ± 2 % ( 70-100% range)\n• Averaging time: user selectable up to 8 seconds\n• Plethysmographic waveform display\n• System must display perfusion index (PI %) from SpO2 as an indication of pulse strength at the sensor site.\n
71	71	6. Temperature\n• 2-channels\n• Continuous digital display of two site temperatures\n• Range: 25-50 degree Celsius\n• Resolution: ± 0.1 degree Celsius\n• Accuracy: + 0.1 degree Celsius\n• Should provide skin temperature probe and rectal temperature probe for every monitor.\n\n
72	72	7. Noninvasive Blood pressure:\n• Capable of measuring blood pressure including in neonates weighing 500 g\n• Microprocessor software with unit in mmHg\n• Oscillometric technique\n• Manual, auto and time limited stat modes\n• User selectable automatic time intervals\n• Display systolic, diastolic and mean BP\n• Blood pressure range\nSystolic : 30-250 mm Hg\nDiastolic : 10-200 mm Hg\nMean: 20 – 100 mmHg\n• Pulse rate range : 20-250 bpm\n• Cuff : auto deflate with over pressure protection\n• Should automatically establish zero reference after each reading\n\n
73	73	8. Invasive Blood pressure\n• At least 2 channels\n• Compatible with reusable and disposable pressure transducers\n• Transducer should allow continuous infusion into the artery through an infusion pump while pressure is simultaneously displayed\n• Input through pressure transducer that functions through a fluid filled catheter system
74	74	· Unit: mmHg\n• Should allow continuous fluid infusion into the artery /vein through an infusion pump without any volume limitation\n• Compatible with arterial BP, CVP and intracranial pressure monitoring catheters with user selectable display names
75	75	· Range 0-350 mmHg\n• Display resolution: ±1 mmHg\n• Accuracy ± 1mmHg\n• Digital waveform display\n• User selectable pressure channel display
76	76	· Should be Compatible with ICP monitoring system\n• Name of manufacturer of compatible ICP monitoring system should be provided with documentary evidence.\n• Monitor must measure dynamic preload parameters such as pulse pressure variation (PPV) and systolic pressure variation (SPV) from arterial waveform and display on main screen.
77	77	9. EtCO2\n• Should provide mainstream modules-2nos and microstream – 2 nos.\n• Warm up time: capnogram displayed in less than 15 sec\n• Measurement method: infrared spectrum\n• Unit: %, mmHg, kPa\n• CO2 Accuracy: +/- 2.0 mmHg\n• Measurement range: 0-150 mmHg\n• Resolution: 1 mmHg\n• Resp rate accuracy +/- 1 rpm\n• Range of resp rate measurement: 0-150/ min\n• Should also be able to monitor Etco2 by non-invasive (nasal) way from the same module.\n
78	78	10. EEG\n• EEG module should be interchangeable with any of the monitors Input: 6 lead\n• Sensitivity: 20, 50,100,250/µV/cm\n• Display: Left or right sided waveform\n• Small, cup type EEG electrodes and lead set kit suitable for neonatal use with a low impedance\n
79	79	11. User selectable alarms\n• High and low heart rate\n• High and low respiratory rate\n• Apnea with adjustable time 5-20 seconds\n• High and low saturation\n• High and low SBP\n• High and low DBP\n• High and low MAP\n• Probe failure\n• Poor signal\n• Power failure\n• Audio & visual alarms with message with separate alarm indicator with 3600viewing.\n\n
80	80	12. Trends\n• Memory storage : at least 72 hours\n• Data display interval : not more than 20 sec\n• Display range : last ½ hour to 72 hours\n• Graphical and tabular format of display of variables\n• Full waveform disclosure of 24 hrs.\n
81	81	13. Power\n• 220/240 V 50/60 Hz AC\n• Rechargeable internal / external battery with a backup of at least 1 hr\n
82	82	14. Manuals: One set of operator & service manuals with each monitor\n15. Comprehensive warranty period: 5 years and CMC for 5 years after warranty\n16. Availability of spares for at least 10 years after date of installation\n
83	83	The following quantities are to be supplied for every monitor with the initial order: ECG/Respiration\n• ECG patient cable : 2\n• Reusable ECG lead wires set : 2 sets\n
84	84	Oxygen saturation\n• Patient extension cables: 2\n• Reusable neonatal wrap around probes: 4\n• Reusable pediatric clip/ finger probes: 4\n
85	85	Temperature\n• Reusable surface (skin) temperature probes: 2\n• Reusable rectal temperature probes: 2\n
86	86	NIBP\n• Patient extension cable – 2\n• Disposable NIBP cuffs suitable for neonates, children and adults (<1000g, 1000-2000g, >2000g, pediatric, adolescent and adult): 5 no of each size.\n
87	87	IBP\n• Transducer connecting cables: 2\n• Reusable pressure transducer: 5\n• Disposable pressure dome kit with neonatal flush device: 10\n• Quotation must include a compliance statement and in addition, each of the above points is marked in the technical brochure. Points not covered in the brochure must be specifically addressed in a separate certificate.\n
88	88	Manuals:\n• One set of operator & service manuals with each monitor\n• Should be able to provide training of all healthcare personnel during first 1 month of installation in the group of 5 trainees per session.\n• FDA (USA) and CE certificate must be enclosed.\n• Onsite physical demonstration of the machine with all standard actual accessories of the same make which the firm intends to supply will be mandatory if demanded by the technical committee.\n• The Machine with all the accessories has to be left in the unit for demonstration on real patients for at least 1 month.\n• Prices of the above consumable accessories should be quoted separately, which will be fixed for the duration of comprehensive warranty and CAMC.\n\n
89	89	5. Pulse Oximeter \nSpecification\n1. Desktop sturdy compact model which is light weight \n2. Resistant to motion artifact \n3. Able to reliably pick up signal in low perfusion states \n4. Should have clinically proven track record to work during motion and very low perfusion conditions \n5. Compatible with reusable and disposable probes	item89	4	Nos
90	90	6. Device should be able to continuous monitor the \nfollowing parameters non-invasively: \na) Oxygen saturation \nb) Pulse rate \nc) Perfusion index \nd) Pleth Variability Index \ne) Total Hemoglobin\nf) Carboxyhemoglobin\ng) Methemoglobin\nh) Oxygen Content \n
91	91	7. Oxygen saturation \na) Display Range 0 to 100 % \nb) Resolution 1% \nc) Accuracy + 3 at 70-100% range \nd) Alarm Range 1% to 99% \n
92	92	8. Pulse rate \na) Display Range 25 bpm to 240 bpm \nb) Resolution 1 beats per minute \nc) Accuracy ± 3 bpm \nd) Alarm range 30 bpm to 235 bpm \n
93	93	9. Perfusion index \na) Display Range 0.02% to 20% \nb) Alarm range 0.03% to 19% \n
94	94	10. Pleth variability index \na) Display Range 0% to 100% \nb) Alarm range 1% to 99% \n
95	95	11. Total hemoglobin\na) Display Range 0 g/dl to 25.0 g/dl \nb) Resolution 0.1 g/dL \nc) Accuracy 8 g/dL to 17 g/dL ±1 g/dL \nd) Alarm range 1.0 g/dL to 24.5 g/dL \n
96	96	12. Carboxy hemoglobin\na) Display Range 0% to 99% \nb) Resolution 1% \nc) Accuracy 1% to 40% ± 3% \nd) Alarm range 1% to 98% \n
97	97	13. Methemoglobin\na) Display Range 0% to 99.9% \nb) Resolution 0.1% \nc) Accuracy 1% to 15% ± 1% \nd) Alarm range 0.1% to 99.5% \n
98	98	14. Oxygen content \na) Display Range 0 ml to 35 ml
99	99	15. Should be able to measure parameters reliably \nin patient < 1kg of weight
100	100	16. Should be defibrillator proof
101	101	17. Display \na. Large bright LCD display with contrast adjustability \nb. Readable from at least 3 feet \nc. Alarms and alarm limits \nd. Status of battery charging, sensor off \n
102	102	18. Alarms \na. Type of alarm Audible and visual \nb. Alarm volume Adjustable \nc. System alarms Probe failure, system failure, low battery \n
103	103	19. Alarm override facility should be present
104	104	20. Trends \na. Memory At least 48 hours with 2 sec resolution \nb. Data interval 20 sec \nc. Display 2-24 hours \nd. Type of display Graphical & tabular display \n
105	105	21. Power \na. 220/240 V AC, 50/60 Hz \nb. Rechargeable internal battery \nc. Battery back-up at least 3 hours \nd. Automatic switch from mains to battery in case of power failure \n
106	106	22. RS 232C interface for data communication
107	107	23. Should have provisions for wireless and blue tooth connectivity
108	108	24. Accessories \ni. Patient extension cables -2 with each monitor \nii. Reusable flexible neonatal multi-site probes-4 with each monitor \n
109	109	25. Operator Manual to be provided. \n26. Should have local service facility and should have the necessary equipments to \ncarry out preventive maintenance test \n
110	110	27. Onsite physical demonstration and training of the equipment to\n all the end users with all the requested facilities will be mandatory \n28. Availability of spares for at least 7 years after date of installation \n
111	111	29. Items covered under warranty/CMC \na) Prices of consumables should be quoted separately and frozen for the period including warranty and CMC period
112	112	30. Standards, safety and training \na) Should be US FDA and European CE approved product and certificate of the offered model must be submitted with the bid documents \nb) Manufacturer should be ISO certified for quality standards Electrical safety conforms to standards for electrical safety IEC 60601-1 (OR EQUIVALENT international/national standard)General requirement for Electrical safety of Medical Equipment Should have local service facility \nc) 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 manual \n
113	113	31. Environmental factors \na) 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. \nb) The unit shall be capable of being stored continuously in ambient temperature of 0-50deg C and relative humidity of 15-90% \nc) The unit shall be capable of operating continuously in ambient temperature of 20-40 deg C and relative humidity of 15-90% \n
114	114	32. Onsite physical demonstration/training of the equipment to\n all the end users with all the requested facilities will be mandatory
115	115	33. Documentation \na) User/Technical/Maintenance manuals to be supplied in English \nb) Certificate of calibration and inspection from factory \nc) List of important spares and accessories with their part number and costing out. \n
116	116	Neonatal Bubble CPAP with oxygen blender \nSpecification\n1. The instrument should be suitable to provide respiratory care in both term and preterm neonates weighing 500 g to 5000 g.	item116	1	Nos
117	117	2. Light weight, portable and sturdy. \n3. Stainless steel stand - corrosion-free, dust resistant, stainless steel \n4. CPAP pressure with oscillations should be generated by creating resistance in water column and bubbling of exhaled gas in the water column. \n5. The system should be suitable for both CPAP and high flow nasal cannula therapy. \n
118	118	6. CPAP generator \n• Pressure: 3 to 12 cm H2O \n• Has detachable overflow container \n• Delivers intended pressure constantly and accurately (+ 1cm) \n• Easy to clean/sterilize \n• Gradations on the sliding rod should be easily visible from a distance of 4 feet.\n
119	119	7. Safety features \n• Limiting the delivered pressure in the event of an occlusion \n• A stand or arm support for holding the circuit in support \n
120	120	8. Humidifier \nIt should be servo controlled heated humidifier with following features: \n• Temperature and flow sensor with feedback mechanism. \n• Monitoring temperature of gas at chamber end and near patient end additionally temperature of airway, chamber and heater plate. \n• Display for temperature of saturated gas. \n• Modes: intubated and mask mode. \n
121	121	Alarms \n• High temperature and low temperature. \n• Water out alarm / POP off pressure adjustment. \n• Heater adaptor faulty/ disconnect. \n• Temp cum probe faulty / disconnect. \n• Hardware faults. \n• Heater wire with adapter to be provided \n
122	122	9. Delivery system \nThe patient heating circuit should have integrated heated coil for uniform heating. \nThe delivery system should have Maximum Input Flow- 15L/min and maximum mean CPAP- 15cmH20. \n
123	123	Humidification chamber should be auto feed with dual float system \nChamber Compressible volume 260- 300 ml \nCompliance of chamber 0.4ml/cm/H20 \nMax peak flow should be 180 L/min. \n
124	124	10. CPAP Bubble generator should have adjustable probe for pressure settings 3-10 cm of H2O.It should have detachable overflow container to maintain constant water level. Volume for generator ~ 500 ml.
125	125	11. Air-oxygen blender \n• The instrument should be suitable to provide air-oxygen mixture to neonates \n• Should be compatible with bubble CPAP system \n• FiO2 concentration will be adjustable (21-100%) and accurate \n• Should be High & Low Flow (Flow rate of 3-30 L/m), accuracy of +/- 3 percentage and bleed flow of 2.5-3.5 \n• Should have stand & pole assembly to incorporate Air & O2 blender with flow meter \n• Should be supplied with connecting tubes and adapter to be attached with oxygen and compressed air source \n
126	126	12. The system should have safety mechanism with pressure relief valve and ports for pressure and FiO2 monitoring. Pressure relief should be 17 cmh20 and above @8L.
127	127	13. Interface \n• Nasal prongs/ masks of silicon of at least five different sizes useful for babies weighing between 750-1250g, 1250-1750g, 1750-2000g, 2000-2500g. Where the resistance to flow at pressure port of nasal tubing should be 0.4 cm H20, 0.6 cmH20 or 0.2 cm/H20.
128	128	· Flexible nasal tubing with glider technology from block and fixing guide with sizes ranging from 50mm to 100mm where resistance to flow should be 0.49 cm/H20,0.53cm/H20, 0.55 cm/H20 respectively flow of 6 lit/min.\n• Infant caps of following sizes: 17-22, 22-25, 25-29, 29-36 cm Circumference. \n• Nasal cannula of preterm and term sizes. Cannula should be kink proof and have hydrocolloid based adhesive to secure on skin and facilitate kangaroo mother care. \n• Nasal masks suitable for preterm and term babies. \n• Nasal masks should be interchangeable to nasal prongs. \n• The mask should be soft and anatomically shaped. \n
129	129	14. It should have mobile trolley to fix Humidifier, CPAP generator and monitor and pole with castors & IV hook and mounting brackets Gas supply lines to blender.
130	130	15. Documentation \n• User/Technical/Maintenance manuals to be supplied in English \n• Certificate of calibration and inspection from factory \n
131	131	16. General requirement for Electrical safety of Medical Equipment \n17. Onsite physical demonstration of the monitor with all the requested modules will be mandatory \n18. Should have local service facility
132	132	19. The service provider should have the necessary equipment’s recommended by the manufacturer for installation and to carry out preventive maintenance test as per guidelines provided in the service/maintenance manual. \n
133	133	20. Patient circuits \na. Disposable circuits should be readily available and reasonably priced \nb. A single patient circuit pack should contain ALL the necessary tubing/connectors needed to assemble a complete circuit \nc. Should have all connections /connecting tube with standard wall fittings /air-oxygen outlets \nd. Should have heater wire in inspiratory limb \ne. Should have water trap in expiratory limb \nf. Should be compatible with available interfaces including nasal masks \n
134	134	21. The entire system including Air oxygen blender should be approved by US FDA or its equivalent National Certifying Authority
135	135	22. Each unit to be supplied with: \n• Disposable circuits: 25 \n• Nasal interface: 25 \n• All size nasal prongs: 10 sets \n• All size head bonnets: 10 sets \n
136	136	23. Prices of above consumables and accessories should be quoted separately in the financial bid. \n24. Comprehensive warranty for at least 5 years.
137	137	25. Good after sales service with at least 3-monthly visits for routine checking and in between whenever called for troubleshooting. \n26. Company should ensure the supply of consumables and accessories for the period of warranty and CMC.
138	138	Portable blood gas analyser\nSpecification\n1. The system is required to analyse blood gases in arterial and venous blood at bedside. \n	item138	1	Nos
139	139	2. It should provide the readings of pH, pO2, pCO2, TCO2, HCO3, base excess, sodium, potassium and haematocrit.
140	140	3. The system should be able to report the values accurately in the range – pH (6.5-8.0), pO2 (40-400 mmHg), pCO2 (10-100 mmHg), TCO2 (5-50 mmol/L), HCO3 (5-70 mmol/L), base excess (-25 - +25 mmol/L), sodium (110-170 mmol/L), potassium (2-8mmol/L) and haematocrit (20-60%).
141	141	4. The process time should be < 5 minutes \n5. The system should preferably have facility for wireless transfer of reports to the hospital information system.
142	142	6. The system should be supplied along with inbuilt printer. \n7. The system should be factory calibrated. The supplier should perform quarterly calibration, to maintain accuracy of the system.
143	143	8. It should have provision to be battery operated. \n9. It should be US FDA/ European CE certified. \n10. It should function at temperature range 15? to 50?. \n\n
144	144	11. Manufacturer should have ISO 9001:2008 certification. \n12. Analyzer should comply with IVD Medical Device Directive 98/79/EC
145	145	Heated Humidified High Flow Nasal cannula Therapy device\nSpecification\n1. Suitable for treatment of Hypoxemic patients with respiratory distress\n2. It should be complaint for use on patients in ICU, wards, emergency department and\nhome oxygen therapy\n	item145	1	Nos
146	146	3. It should be single system for treating infants, paediatric and adult patients\n4. Inbuilt flow generator capable of delivering wide range of flows:2-25 litres in\npaediatric mode and 10-60 litres in adult mode\n
147	147	5. Inbuilt Air/O2 blending and Fio2 monitoring, facility to deliver wide range of oxygen concentration (Fio2) from 21 to 100%\n6. It should have inbuilt Air source without need for external compressor\n7. Integrated heated humidifier
148	148	8. Color display to monitor humidity setting, flow, Fio2 and faults\n9. Visual and audible alarm indication for:\na. Tubes disconnect leaks, tube blockages and water out and hardware fault with error codes. Audible power failure alarm\n
149	149	10. Disinfection mode with heated disinfection tube for sterilization of the device after patient use\n11. Supplied with heated wire patient breathing tube and nasal cannula of different sizes\n12. Paediatric nasal cannula should be made of kink proof material and has adhesive\nwiggle pads to stick on skin to facilitate kangaroo care\n
150	150	13. It should be compatible for use on tracheostomy patients\n14. Should have safety certificate from a competent authority CE issued by a notified body\nregistered in the European commission / FDA (US)/ STQC CB Certificate/ STQC S\nCertificate or valid detailed electrical and functional safety test report from ERTL. Copy\nof the certificate/ test report shall be produced along with the technical bid\n
151	151	15. Complaint with international safety standards and regulations.\n
152	152	9.Cash cart \nSpecification\n1. Size -940x490x1535 mm approx. \n2. Trolley with 25 mm diameter SS tubular frame\n 3. Drawers maximum number possible of adequate size	item152	4	Nos
153	153	4. Flat surfaces should be stainless steel. \n5. Two/three rows of hand out bins of different size &color to hold different sizes of ampoules/vials of emergency medicine.
154	154	6. Light weight plastic box with drawers of different sizes and colors \nto hold emergency medicines, ambu bag, IV solution , catheters etc separately. \n7. Facility to carry monitor & suction apparatus. \n8. Stainless steel saline rod-one.
155	155	9. Castor wheels of 12.5 cm diameter with two having locking arrangement.\n10. Pull out cardiac massage board above drawers. \n11. Oxygen cylinder stand on one side. \n12. All parts should be epoxy polyster coated with 50 micronethichness approx. ebonite rubber , PVC and castor wheel etc. \n13. Whole crash cart should be washable.
156	156	Radiant Baby Warmer/ Neonatal resuscitation unit\nSpecification\n1. Essential parts \na) Quartz based warming system with microprocessor based controls, probes & alarms \nb) Cart & bassinet \nc) Examination light \nd) X-ray cassette holder \n	item156	2	Nos
157	157	2. Cart \na) Should swivel on 4 wheels of at least 4” diameter with foot operated brakes on at least 2 front wheels
158	158	3. Dimensions \na) Height - 180- 200 cms\nb) Width - 65-80 cms\nc) Depth - 100-120 cms\nd) Working level - 95-105 cm \n
159	159	4. Bassinet \na) Collapsible transparent acrylic side walls
160	160	5. Mattress \na) Width - 70 - 80 cms\nb) Length - 90 - 100 cms\nc) Thickness - 3-5 cm \nd) Material \ni. Soft and easy to clean \nii. X-ray transparent \niii. Fire retardant \niv. Allows air to pass through but does not allow water to seep in \n
161	161	6. Bassinet tilt \na) Should allow tilt for Trendelenburg as well as reverse Trendelenburg position
162	162	7. Warming system \na) Quartz based heating system encapsulated heater tube placed in a parabolic reflector \nb) Should have single element quartz infrared heater \nc) Control - Microprocessor controlled \nd) Self-test function performed at power on \ne) Digital display should show following parameters \ni. Set temperature \nii. Present temperature of the baby \niii. Heater output \niv. The temperatures should be in numerical LED display\n
163	163	f) Mode - Manual & skin (servo) \ng) Manual mode \ni. Adjustable in steps from 0 to 100% in increments of 10% \nii. Heater power should be reduced to 50 - 60% after 10-15 minutes in manual mode for baby safety \n
164	164	h) Skin mode (servo mode) \ni. Set point range - 32 – 38 degrees C \ni) Skin temperature display \ni. Accuracy - ±0.2 degrees C \nii. Resolution - 0.1 degree C \nj) Temperature probe- Wire should be easy to clean and long lasting \nk) No need of temperature probe calibration \n\n
165	165	8. Alarms \na) Audiovisual alarms with a display of text messages about the alarms \ni. Probe failure \nii. Heater failure \niii. High and low baby temperature (more than 0.5 deg C difference) \niv. Power failure \nv. System failure \nvi. Silence/reset switch \nvii. Should have Automatic cut-off of heater at 39°C for Over Temperature Protection \n
166	166	9. Heating unit - Should be swivable for accommodating X-Ray unit and\n should have self-lock facility.
167	167	10. Examination light \na) Illuminance - at least75 foot candles at mattress centre \n11. Apgar Timer \na) Timer with stopwatch facility \nb) Reset facility \n
168	168	12. I.V. stand \na) Strong IV stand (S.S) with height adjustable and facility to fix large number of infusion pumps
169	169	13. Monitor shelves - Two in number \n14. Should have T piece resuscitator inbuild inside with standard recommendation for neonatal resuscitation.\n15. Should have two drawers \n
170	170	16. X- Ray cassette holder \na) Sliding holder located just below undersurface of bassinet, with markings to help placement of cassette
171	171	17. Power consumption - Less than 1 K.W
172	172	18. All metal parts of the equipment should be corrosion resistant and Epoxy/Powder coated
173	173	19. All consumables required for installation and standardization of system to be given free of cost
174	174	20. Standards, safety and training.\na) Should be European CE approved product and certificate needs to be submitted along with the catalogue \nb) Manufacturer should be ISO 13485 certified for quality standards \nc) Electrical safety conforms to standards for electrical safety IEC 60601-1 (OR EQUIVALENT international/national standard)General requirement for Electrical safety of Medical Equipment \nd) Should have type of protection against electric shock: Class 1 \ne) Should have degree of protection against electric shock: Type B \n
175	175	21. Power supply and electrical specifications \na) Power input to be 220-240VAC, 50Hz \nb) Suitable Autovoltage corrector with spike protector should be available \nc) Should have overload protection at 4A \nd) Should have leakage current <0.5mA \ne) Should have earth resistance <0.2 Ohm \nf) Should be Low Noise \ng) Fuse Rating should be \ni. For main supply: for 230V: 4A & for 110V: 8A \nii. For examination lamp: for 230V: 2A & for 110V: 2A \n
176	176	22. Enviornmental factors \na) Shall meet IEC-60601-1-2 :2001 General Requirements of Safety for Electromagnetic Compatibility or should comply with 89/366/EEC; EMC-directive \nb) The unit shall be capable of being stored continuously in ambient temperature of 10-55 deg C and relative humidity of 15-90% \nc) The unit shall be capable of operating continuously in ambient temperature of 20- 40 deg C and relative humidity of 15-90% \n
177	177	23. Documentation \na) User/Technical/Maintenance manuals to be supplied in English \nb) List of important spares and accessories with their part number and costing \n
178	178	24. Essential accessories to be supplied at initial purchase with each piece of equipment \na) Reusable temperature probes (full set): 5 nos/per equipment.
179	179	25. The rates of consumable accessories should also be quoted separately\n26. Onsite physical demonstration/training of the equipment to all the end users with all the requested facilities will be mandatory.
180	180	ICU Beds \nSpecification\nSize approx. 2160mmL x 1020mmW x 450mm to 810mm Height (without Mattress) \nBed Platform size: 2070mm L x 960mm W; Mattress Platform size: 1900 mm L x 865 mm W
181	181	Five section Polypropylene detachable tops fitted on four section top bed frame with perforated design for easy breathing of mattress
182	182	Back rest and leg rest both shall have detachable mattress guards (3 nos. on each section respectively)
183	183	Back rest: min. 45% of the frame length
184	184	Should be able to adjust Back rest, knee rest, height adjustment and trendelenburg /reverse trendelenburg positions using lever.
185	185	Backrest and knee rest shall retract as they are individually and simultaneously raised
186	186	Bed frame shall be mainly made from 50 x 25mm x 2mm thick ERW tube with proper support.
187	187	This frame should be fitted on the base frame mainly made of 60 x 30 x 1.6mm ERW tubes on various supporting links
188	188	The base frame shall be mounted on 125 mm dis non-rusting twin wheel castor with central & directional locking mechanism
189	189	Twin wheel castors with castor housing and wheels made from high grade non floor staining synthetic materials and integrated thread guards. Wheel centre having precision ball bearing to run smoothly
190	190	The bed shall have polymer moulded head and foot side panels detachable by hand without need of any tool. Four corner rubber buffers
191	191	Bed shall have split type swing down railing, 2 on each side (head and middle sections) made from polymer moulded material. These shall be fitted to the mattress support sections and should be able to raise and lock through spring lock mechanism through an operating lever. When put down, they should undergo and level with bed frame
192	192	Railing shall avoid any finger and neck entrapments and comply with IEC standards 60601-2-52
193	193	31.7mm dia; 18G stainless steel outer covering tube with a knob to mount syringe pump \nBuilt-in bed extension of approx. 200mm shall be provided
194	194	Accessories: \n12mm diameter stainless steel SS304 telescopic heavy duty IV rod with 2 hooks with provision to park when not in use \nUrine bag holder – one \nChart holder – one \n
195	195	Four section mattress with 4 inch thick PU Foam of 40 density, covered with superior cover material (water proof, anti- bacterial and flame retardant properties) Oxygen cylinder Cage
196	196	DEFIBRILLATOR- CARDIOVERTER WITH ECG MONITOR\nSpecification\n1 Description of Function\n1.1 Defibrillator is required for reviving the heart functions by providingselected quantum of electrical shocks with facility for monitoringvital parameters.	item196	1	Nos
197	197	2 Operational Requirements\n2.1 Defibrillator should be Bi- Phasic, light weight and latest model\n2.2 Should monitor vital parameters like ECG, heart rate etc. and display them\n2.3 Should print the ECG when required.\n2.4 Should work on Manual mode (0-200J or more).\n2.5 Should be capable of doing synchronized & asynchronized cardioversion both.\n2.6 Can be operated from mains as well as battery.\n2.7 Should have defibrillator testing facility.\n\n
198	198	2.8 Facility for trans-cutaneous pacing and trans-venous pacing\nshould be available\n2.9 Demonstration of the equipment is a must.
199	199	3 Technical Specifications\n3.1 Should be a Low Energy Biphasic defibrillator monitor with Recorder, having capability to arrest all arrhythmia within a maximum energy of 200 Joules for manual mode.
200	200	3.2 Should monitor ECG through paddles, pads and monitoringelectrodes and Defibrillate through pads and paddles. Should have Automatic or Manual Lead switching to see patient ECG through paddles or leads
201	201	3.3 Should measure and compensate for chest impedance\n3.4 Should have a built in printer/ thermal recorder.\n3.5 Should have minimal charging time for maximum energy with charging indicator (mention the time in the bid – shorter is preferred).
202	202	3.6 Should have bright LCD/TFT display for viewing messages and ECG waveform\n3.7 Adult and paediatric paddles should be available\n3.8 Should have event summary facility for recording, printing and patient data storage of ECG and events.\n
203	203	3.9 Should have a battery capable of usage for at least 60 minutes or 30 discharges\n3.10 Should be capable of printing Reports on Event summary, configuration, self-test, battery capacity etc\n3.11 Should have facility for self-test/check before usage and set up function\n3.12 3.12 Should be capable of delivering energy in increments of 1-2 joules up to 30J and increments of max. 50J thereafter. (Narrow increments preferable)\n3.13 Should have user friendly colour coded operation.\n
204	204	4 System Configuration Accessories, spares and consumables\n4.1 Defibrillator -01\n4.2 Paddles Adult & Paediatric -01 each\n4.3 Patient cable -01\n4.4 ECG Rolls -5\n4.5 Disposable pads-5 nos.\n4.6 Complete set of ECG Leads- 02\n4.7 Price has to be quoted inclusive of the above (4.1 – 4.6) items and\nseparately for the accessories and consumables as mentioned (4.2 –\n4.6).\n
205	205	5 Environmental factors\n5.1 The unit shall be capable of being stored and operating\ncontinuously in ambient temperature of 10-40?C and relative\nhumidity of 15-90%.\n
206	206	6 Power Supply\n6.1 Power input to be 220-240VAC, 50Hz\n6.2 Resettable overcurrent breaker shall be fitted for Protection.\n
207	207	7 Standards, Safety and Training\n7.1 Should be USFDA and European CE approved product.\n7.2 Electrical safety conforms to acceptable standards (provide certificate)\n7.3 Should conform to international test protocols on exposure to shock forces and to vibration forces. The standard should be documented.\n7.4 Should have local service facility with necessary equipments recommended by the manufacturer to carry out preventive maintenance test as per manual.\n
208	208	8 Documentation\n8.1 User Manual & Service manual in English\n8.2 List of important spare parts and accessories with their part number and costing\n8.3 Certificate of calibration and inspection from factory.\n8.4 Log book with instruction for daily, weekly, monthly maintenance checklist. The job description of the hospital technician and company service engineer.\n
209	209	8.5 List of Equipments available for providing calibration and routine maintenance support.\n8.6 Compliance Report to be submitted in a tabulated and point wise manner clearly mentioning the page/Para number of original catalogue/data sheet. Any point, if not substantiated with authenticated catalogue/manual, will not be considered.
210	210	8.7 Must submit user list and performance report within last 5 years\nfrom major hospitals/government hospitals.
211	211	Warranty for 3 Years\nAMC for 5 years.
212	212	Automatic double breast pump\nSpecification\n1. Unique programmable breast pump available with program card with initiate, build & maintenance program.
213	213	2. Breast pump should be electrical & battery operated. \n3. Should have LCD display; equipped within internal rechargeable batteries. \n4. Should be made up of hospital grade material for use by multiple mothers and heavy duty. \n
214	214	5. Parts should be cleanable and sterilisable easily without any damage. \n6. Double pump: must be able to pump both breasts at the same time to get more and better-quality milk. \n7. Two phase expression technology: designed to mimic baby’s sucking pattern to optimise milk output i.e., stimulation followed by expression.
215	215	8. Should be a closed system; membrane cap & diaphragm should be attached to breast pump machine only. No diaphragm & membrane cap should be attached to collection bottle.
216	216	9. Pump should automatically change mode after 2 minutes; changes from stimulation to expression mode; Along with this, there should be facility to change mode individually.
217	217	10. Pump should be portable with weight of 3-4 kg \n11. Live demonstration and training of end users for the equipment is must. \n12. Catalogue/Brochure should be submitted along with technical bid mentioning each and every point of technical specification. \n13. Pump should be European CE/US FDA/ISO approved. \n14. Breast Pump should have Protection Class II, Type B \n
218	218	15. 5 years’ comprehensive warranty. Company should ensure the supply of consumables and accessories for the period of warranty and CMC.
219	219	16. Availability of spares from installing date must be there for a period of at least 10 years.
220	220	17. The bidder must be a manufacturer or its authorized agent.
221	221	18. Mandatory accessories/consumables should be from same manufacturer: - \n• Tubing, Breast shield- 24mm, Valve membrane) – 40PCS \n• Disposable milk collection bottles 150 ml : 40 pcs \n• Bottle Stand- 01 \n
222	222	19. Should construct and fabricate four breast feeding chambers in the designated breast feeding room.
223	223	20. Documentation \n• User/Technical/Maintenance manuals to be supplied in English \n• Certificate of calibration and inspection from factory \n
224	224	21. General requirement for Electrical safety of Medical Equipment.
225	225	T piece resuscitator \nSpecification\n1. Should be manually operated, gas powered resuscitator with consistent Peak Inspiratory Pressure(PIP) and Positive End Expiratory Pressure (PEEP) to infants.
226	226	2. Should accept and deliver oxygen concentrations from 21% to 100%.\n3. T-piece circuit should be connected to infant resuscitation masks or endo tracheal tubes. \n4. The gas flow outlet should allow easy and secure connection of T-piece circuit and humidified T-piece circuit. \n
227	227	5. Manometer range : -10 to 80 cmH20; ± 2% accuracy \n6. Maximum pressure relief : 8L/min 5 to 70 cmH20 \n7. Peak Inspiratory Pressure : 5L/min 2 to 70 cmH20 8L/min 3 to 72 cmH20 10L/min 4 to 73 cmH20 15L/min 8 to 75 cmH20 \n8. Input gas flow range : 5L/min (minimum) to 15L/min (maximum) \n9. Should be supplied with the following accessory a. Gas supply line – 3 Nos \n
228	228	10. Should be supplied with the following consumables \na. Disposable infant resuscitation Tpiece circuit – 10 Nos \nb. Disposable infant resuscitation Tpiece mask – 10 Nos \nc. Disposable humidifier T-piece circuit with heated wire – 10 Nos
229	229	11. Should have safety certificate from a competent authority CE issued by anotified body registered in the European commission / FDA (US)/ STQC CB Certificate/ STQC S Certificate or valid detailed electrical and functional safety test report from ERTL. Copy of the certificate/ test report shall be produced along with the technical bid
230	230	Spot light\nSpecification\n1. Central illumination intensity at a distance of 1 meter: minimum 30000 Lux \n2. Central illumination intensity at a distance of 0.5 meter: minimum 70000 Lux	item230	1	Nos
231	231	3. Light field diameter at a distance of 1 meter: minimum 165mm \n4. Light field diameter at a distance of 0.5 meter: minimum 110mm \n5. Color Temperature: minimum 4500 K \n6. Color Rendering index (Ra) in every color temperature setting: 90 or more \n7. LED Life time: minimum 50000 hours \n
232	232	8. Should be mounted on stable mobile stand with at least five wheels. \n9. Stand should have hinged arm on which the light is mounted. \n10. Light should be height adjustable and angle adjustable. \n11. Class II Medical Electrical Equipment Protection (IEC 60601-1) \n
233	233	12. Light Housing Ingress Protection Class (IEC 60601-1 & IEC 60601-2-2): IP20 or better \n13. System should have BIS/ US FDA/ European CE with four-digit no. certificate for the intended use.
234	234	Cardiac Table	item234	3	Nos

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Supply And Installation Of Picu/Nicu Equipments For Igh Kavaratti Supply , Installation , Commissioning , Provide 3 Years Comprehensive Warranty And 5 Years Camc After Expiry Of Warranty Period For The Picu/Nicu Equipments For Igh Kavaratti, Lakshadweep-Lakshadweep

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Supply And Installation Of Picu/Nicu Equipments For Igh Kavaratti Supply , Installation , Commissioning , Provide 3 Years Comprehensive Warranty And 5 Years Camc After Expiry Of Warranty Period For The Picu/Nicu Equipments For Igh Kavaratti, Lakshadweep-Lakshadweep

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