HLL Infra Tech Services Limited Tender

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HLL Infra Tech Services Limited - HITES Tender

Services

Healthcare and Medicine

Eprocure

Gautam Buddha Nagar, Uttar Pradesh

Opening Date17 Feb 2024

Closing DateCancelled

Tender Amount₹ 6,56,12,020

Notes

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Costs

EMD
₹ 13,12,240
Document Cost
₹ 5,900
Tender Fee
Refer Documents

Description

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Tender Id
2024_HITE_186991_1
Bid Award Id
View
Tender No
HITES/PCD/AIIMS BPL/RT-IVF/23-24
Tender Authority
HLL Infra Tech Services Limited View
Purchaser Address
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Website
http://etenders.gov.in

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BOQ Items

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Mini Incubator

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Anti-Vibration table

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Electronic Witnessing System

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VOC Meter

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PH Meter for IVF Media Monitoring

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Temperature Meter for IVF Instrument Monitoring

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Gas Analyzer

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Portable Air Purification Sysytem

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Denudation Pipette

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Sperm Counting Chamber

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Class I 6*2 Feet Dual IVF Workstation with Integrated RF ID Based Witnessing System

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Premix Benchtop Incubator for Human Embryo Culture with Humidification

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Trinocular Compound Microscope for Andrology

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Class I Laminar Flow Cabinet for Andrology 6*2 Feet

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Clinical Centrifuge for Andrology

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Dry Incubator Andrology

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CO2 Incubator

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Oocyte Aspiration Pump

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Liquid Nitrogen Container with Wheels

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8i-10 KVA Online UPS with 1 Hr Battery Back Up

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Pharmaceutical Refrigerator

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B. Management and treatment of Patients: IVF Cycle (Annexure B)

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Medicines (To support Infertility Treatment)

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Hormones (To support Stimulation for ART cycle)

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Media (To support Embryo/Blast Development)

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Consumables (To handle Human Gametes)

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Disposables (For Lab Management)

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Aim: Teaching & Training Knowledge Transfer Practical Hands on Skill Development

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Offer training programs catering to

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Clinicians

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Embryologists

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Lab Managers

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Centre Managers

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Bio-medical engineers

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Lab Technicians

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Offer orientation programs to help the participants understanding the processes in ART

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The purpose of these courses is skill enhancement and knowledge upgradation as part of continuous quality improvement.

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Options for Embryology lab related training modules at IKDRC ut6

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Quality control in ART laboratory (2 days)

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Laboratory Management: Maintenance & Calibration (2 days)

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Safety and troubleshooting in an ART laboratory (2 days)

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Orientation of an ART Cycle (5-7 days)

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ICSI & Biopsy training ( 3-5 days)

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Cryopreservation of human gametes (2-3 days)

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Key Responsibilities for the Project

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Comprehensive development of IVF lab

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Processing for the necessary Approvals,Registrations, Permission from the regulatory bodies of ART. The official fees for the process shall be paid by the Institute.

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Support for indigenous research and development in field of human ART.

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Working together for data monitoring and analysis for establishment for state infertility dashboard.

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General Technical Specifications

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Item 01: Digital Test Tube Warmer for Andrology and Embryology

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Unit should have stainless steel construction

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Unit should have minimum 1-1 each block for min 4-6 test tubes of 5ml & 14ml

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Ideal for all sample tubes requiring a stable heating environment.

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Digital temperature readout

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Unit should have microprocessor based digital controller

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Should be European CE/US FDA/BIS certified

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Visible digital LED display indicates the temperature level

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Easy to clean surface

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Temperature level is adjusted directly on the display in increments of 0.1•c

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Item 02: Benchtop Incubator for human embryo culture with Inbuilt gas mixer

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Bench Top Incubator with excellent control and accuracy of pH, temperature and humidity.

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Between 8-10 chambers for placing Petri Dishes. And one chamber at least can accommodate 2 dishes at a time.

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Each Chamber must have an excellent heat distribution using fully contact heated plates. Tightly packed, full surface heating elements: to create stable environment from heated base and lid.

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Each chamber must have independent display of gas and temperature.

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In built Gas mixer must be there to mix the CO2, N2 & 02.

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24 hours digital recording of temperature and gas flow

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Each chamber preferably must have a heated lid.

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Automatic gas purge in lid closure to maintain gas environment

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Bench top incubator should have reduced oxygen culture capacity.

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Constant Temp 37°C in the dishes.

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Fast recovery. In built alarm alert to low CO2 and temperature

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Power- Universal input 100-240 V, 50/60 Hz.

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Alarm system in case of power failure.

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Inbuilt disposable Gasline filtration system.

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Should have UV-C decontamination of air stream

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Should have validation outputs and pH electrode port

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Should have data logging system, alarm.

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Must be US FDA or EU CE or BIS Approved.

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Low noise level

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Non inductive heating system to provide no electromagnetic fields around the embryos

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Insulated chambers and 10 temperature sensors for quick and precise temperature control

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Must be supplied with Stacking System of 230V with capacity to accommodate at least 3 incubators

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Item No 3: Complete ICSI System(with Inverted Microscope and Micromanipulator)

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Inverted Microscope basic unit

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Suitable modulation contrast system (complete) for Intra cytoplasmic sperm injection (ICSI)

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Good optics.

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Sturdy Stand with built in LED Transmitted light illumination.

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Micromanipulator should be mechanical with digital display of 3D fine control movement from single lever

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Sx nosepiece to accommodate up to five different Objectives. i.e 4x, lOx, 20x, 40x

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Oil/air system for pipette setting and control

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Micromanipulator should be compatible for the utility of commonly available LASER

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Eye piece should be lOX/lSX wide angle.

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Micro tool holder with 2 axis movement for quick setup of micro tools.

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XYZ fine micromanipulator with minimum 10mm of traverse in each direction.

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AIR Syringe for Holding the Oocyte.

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Oil syringe for injections of sperms.

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Should be supplied with center heating system at central hole.

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Must be US FDA or European CE or BIS certified.

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Must provide a software for Video and Image capturing.

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Stopwatch preferred for monitoring the time of manipulation.

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Built-in software with manipulator for picture and Video recording of procedure.

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Fast micropipette set-up with one-step angle adjustment in Air.

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Item No 4: Mini Incubator

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Unit should be Easy to use and compact in size. Approx. dimensions 270x337x95mm

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Ideal for ICSI procedures or to be used inside a Workstation.

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Should reduce embryonic stress during handling for instance when performing ICSI and for short term incubation of oocytes.

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Low consumption of premixed gas

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Built-in humidified Gas System

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Automatic gas purging function which quickly returns the pH to the physiological range

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Must have Two heated chambers that can accommodate up to four warming blocks

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Certificate: Should be CE or US FDA or BIS certified.

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Item 05: Antivibration Table

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The table is adjustable for all available models of inverted microscopes incl. motorized models.

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A mass and a stiff support spring system to ensure fast dampening.

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Space for mini incubator.

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The microscope platform of the anti-vibration table does not touch the actual table.

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Enhance the use of the anti-vibration table and work with an incorporated monitor arm.

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Should be European CE/US FDA or BIS certified.

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Stainless steel shelf for accessories.

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Easy to clean surface.

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Item No 06: Electronic Witnessing System

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One work area required for each critical working location and work on RFID technology. Microsoft Windows based PC or Tablet needed for each work area. Readers available heated. RFID reader frequency: 13.56MHz

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Compatible with GSl barcodes.

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Compatible with USB (Keyboard wedge) fixed and handheld scanners

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Compatible with Operating Systems: Windows 10, Windows 8.1, Windows 7, Windows XP

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Information data allows to make informed decisions about laboratory work improvements.

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Procedure data can be explored in detail or summarized into pie or bar charts.

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Patient samples can be tracked as they enter and leave Cryo storage.

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On thawing/warming, the barcode information is linked automatically with the embryo thaw dish.

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Can enter data directly into patient records using small touch screen displays or a keyboard and mouse interface installed at your work areas.

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System should Input data directly, transcription errors are minimized, and multiple data handling is avoided. Data can be accessed and analyzed immediately.

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Ongoing patient Information is displayed on a big screen fixed to the lab wall and can be accessed from any networked PC.

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Records can be sorted and filtered in various ways to cross-reference patient cycles and material batches.

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Capture images and videos from every microscope in the laboratory, at any stage of the patient cycle.

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Work areas can be connected through Wi-Fi or LAN cables to a central server which means everything works together and data updates in real time.

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Every process in every part of the lab is automatically detected, logged and protected.

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Bespoke flow chart designed by hospital and works in line with existing Standard Operating Procedures (SOPs). Flow chart easy-to-use software interface allow lab to amend the diagram as changes in SOPs and needs evolve.

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Should be European CE/US FDA/BIS certified.

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RFID tags should be available in different size and shapes.

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Item No.07 : VOC meter

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Perform by Photo-ionisation detector (PID) technology 0.1 to 30 ppm

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Operating humidity should be 0% to 95% relative humidity (non-condensing)

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Operating range -10°C to 50°C

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Deleted

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Item No.08: pH meter for IVF media Monitoring

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Should have pH accuracy± 0.02 pH

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Suitable for use with all popular incubators including benchtop versions

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Must have 2-point calibration at room temperature followed by 1 point at 37°C

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Temp accuracy should be ±0.s°C / 0.9°F

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2GB internal memory

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Data export to PC with dedicated software provided

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Item No.09: Temperature meter for IVF Instrument Monitoring

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UKAS-certified offset. Measurement at calibration temperatures repeatable to ±0.2°C

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Should have certification points S°C (41°F) 37°C (98.6°F) 45°C (113°F)

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Typically, 500 hours operation time on battery

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15.5cm x 6.7cm x 4.0cm

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Unique microprobe for micro drop measurement

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Ergonomic design with large backlit digital display

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Item No: 10: Gas Analyzer

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Co2 range: 0-20%

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02 range:0-100%

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Response Time: CO2 equal to 20 seconds 02 equal to 60 seconds

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Built-in gas moisture removal

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Quick verification of incubator concentration levels

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Item no.11: Portable Air Purification system

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clinically proven for safe and effective use in human ART laboratories

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All products are clinically proven for safe and effective use in human ART laboratories

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The ultimate effective air technology to purify VOCs (Volatile Organic Compounds) and pollutants

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High Performance 4-stage Filter system has been proven to improve air quality and may increase expected outcome and overall results

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Certificate: Should be European CE or US FDA or BIS certified.

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Item No.12: Denudation Pipette

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Pipetter should design to be flexible, unbreakable, and will not scratch culture dishes

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Pipetter should design for all sizes necessary for oocyte denudation

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Pipetter should design for manipulation and transfer of embryos or cumulus oocyte complexes, as well as for PGD/blastomere work are available.

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Pipetter should available in a variety of ergonomic handles to match every preference

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Item No.13: Sperm Counting Chamber

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simple-to-use device for rapid and accurate sperm count, motility and morphology evaluation, from undiluted semen specimen

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The lower part has a metal base and two handles. In the center of the base there is a flat disc made of optical flat glass on which the sample is placed.

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The upper part is the cover glass encircled with a metal ring. At the center of its lower surface there is a 1mm2 grid, subdivided into 100 squares, each one of 0.1 x 0.1 mm.

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When the cover glass is placed on the four tips, the space bounded in a row of 10 squares is exactly one millionth of ml. Therefore, the number of sperm heads in 10 squares indicates their concentration in million/ml.

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The depth of 10 microns eliminates blurring and allows sperm to move freely. The applied sample is observed in one focal plane.

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The grid is on the cover glass. This eliminates the need to insert a grid into the microscope eye piece and remove it when not required.

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Reusable. Easily cleaned with a non-bleach disinfectant solution

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Repeated use with complete accuracy without calibration

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Item No.14: Class I 6x2 Feet Dual IVF workstation with Integrated RFID based Witnessing system

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IVF Workstation 6 feet with option of mounting 2 stereo microscope.

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Size: Working chamber should be 6x2 Feet.

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HEPA filters: Class H-14 HEPA Filters in accordance with EN1822. Filter Efficiency 99.999% for 0.3 Micrometer particles size.

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Filters: Pre-Filter and HEPA Filter.

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Heating: Electrical

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Flow: Flow meter to regulate flow rate of gas through bubble flask (vertical Flow)

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Noise level: up to less than 53 Db

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Light damping facility to adjust light intensity.

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IVF Workstation should be vertical and Class I where Sample must be protected from contamination.

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Working chamber tabletop should be made up of stainless steel. SS table should be integrated with two RFID based Witnessing system with heated platform and glass heating RFID reader.

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Integrated Humidification System.

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IVF workstation should have with integrated heated system for two Stereozoom microscope

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Special Heating Surface with Temp accuracy ±0.l-0.3*c

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Inbuilt LCD monitor screen 20' to 22' for display and training purpose.

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Should have minimum 2 Electrical Sockets

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2 Warming blocks for holding at least 8 or more follicular fluid tubes of 14/lSml.

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2 Warming blocks for 60mm dish.

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Must be CE or US FDA or BIS certified

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2 x Microscope Light Opening with Heated Glass of 90 mm.

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Item No.15: Premix Benchtop Incubator for human embryo culture with Humidification

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Designed to maintain consistent culturing environments for optimum temperature and pH control.

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Network connectivity for data output

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Base plate of chamber designed to fit commonly used IVF dishes

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Integrated battery backup for 2 hours

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Reduced oxygen culture capability

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Incubator works with any defined premixed gas of choice to achieve the proper CO2 and reduced 02 environment

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Optional fitted pH monitoring

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Pip-in Window to check water level & Gas Flow without disturbing culture

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Dishes per chamber: 1. 4 x NUNC 4 well dishes; 2. 4 x NUNC 60 mm dishes; 3. 10 x NUNC 30 mm dishes; 4. 4 x MINITUB 5 well dishes; 5. 4 x FALCON 60 mm dishes; 6. 4 x FALCON 60mm single - well "organ culture" dishes

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Must be US FDA or EU or CE approved.

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Item No.16: Trinocular Compound Microscope for Andrology

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Standard microscope set complete with built-in 6V20W halogen light illuminator with regular power supply

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Quadruple ball bearing nosepiece, co-axial coarse and fine focusing controls, high resolution Semi-Plan Achromat objectives 4x, 10x, 20X

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360° rotatable inclined binocular tube, fungus resistant optics for tropical use, widefield paired eyepiece HWF10x (F.N.18), right hand control co-axial low drive mechanical stage and rack & pinion focusable Abbe condenser 0.9/1.25 N.A with iris diaphragm complete set in thermocole packing

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Trinocular Microscope with CCD camera

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Item No.17: Class 1 Laminar Flow Cabinet for Andrology 6x2 Feet

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6x2 feeet LAF where both user and product are protected against particle and microbial contamination in IVF.

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Low Noise levels.

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Should be US FDA/ CE/BIS certified

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Surgical Stainless Steel (2mm) work surface

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Toughened glass front window

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Adjustable luminosity

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Fully operated with a microprocessor control panel.

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USB data output

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Electrical outlets

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Fixed support Stand (80-85cm)

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Approx. Dimensions: 1800x800x2000 (WxDxH)

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Item No. 18: Clinical Centrifuge for Andrology

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Brushless Motor Capacity (6x10ml) with Swing Out Rotor

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Max RPM/RCF (xg)-4000RPM/2270g based on the rotor

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Speed setting as 500-4000 RPM in steps of 10RPM

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User should be able to set and save up to 99 user defined programs (protocols) with a digital display

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Item No.19: Dry Incubator Andrology

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Unit should have stainless steel construction

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Unit should have minimum 14-liter capacity.

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Ideal for warming of all plasticware prior to use.

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Incubator should maintain 37°C.

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Easy to clean surface

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Temperature level is adjusted directly on the display.

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Item No.20 CO2 Incubator

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160 litres internal Volume

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TC/IR CO2 Sensor Soft touch key pad

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Out Door Heating Error Warning

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Auto Start Function

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Inner Safety glass door

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HEPA Filter for CO2

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Inner safety glass screen (3 pieces)

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Microprocessor PID temperature controller

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Temperature Sensor

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Temperature range ambient above 5°C to 50°C (± 0.l°C at 37°C)

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Air- Jacket direct heating system

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Over- Temperature Protection Smooth inner casing with rounded corners on all sides made of stainless steel Dry or Moist heating disinfect ion at 90°C to 120°C.

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Disinfection duration 12-13 hrs

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At least 3 inner shelves

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Must be CE/US FDA/EU/BIS certified

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Co2 Incubator must be supplied with its Table.

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Item No 21: Oocyte Aspiration Pump

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Technical Specifications

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The vacuum pump should have a Cut Off after a set vacuum range is achieved.

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The Low Vacuum should be of minimum range of 300mmHg and high should be of minimum range S00mmHg.

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The vacuum range can be set digitally and the desired vacuum should increase by 1 mmHg.

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The operating switch to create vacuum should be a foot switch.

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There should be toggle switch or system to instantly create high vacuum up to 500mmHg.

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Item No.22 Liquid Nitrogen Container with wheels

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Technical Specifications

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For specimen storage - 47 Litres

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For Liquid Nitrogen storage - 26 Litres

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Item 23: 8-10 KVA Online UPS with 1 hour Battery Backup

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Item Description

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SMF battery backup with 1 hour battery backup with SNMP and isolation transformer, battery rack inter connection links (42AH*20 nos)

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Rectifier & Inverter with IGBT and DSP Technology.

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Voltage 400 ± 15% V, 3 Phase, 4 Wire.

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Frequency: 45 to 55 Hz.

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Display: Control Panel with LCD Screen.

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Battery: Sealed Maintenance Free Rechargeable.

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Back up: 1 Hr (60 Mts)

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Protection: Overload & Short Circuit.

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Ventilation: Forced Air Cooling.

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Item 24: Pharmaceutical Refrigerator

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Item Description

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Capacity of storage 300 liters or more

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Temp range-should have adjustable temperature control range from +1° to +8° C, factory present at 4• C.

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Refrigerator system: The system should have high density CFC-free insulation to protect cabinet from ambient temperature fluctuation. The system should have positive, force, air circulation to maintain temperature uniformity at all shelf levels, with quick recovery+/- 1 degree Celsius. The system should have sensors for activation of automatic/manual defrosts cycle to minimize the frost build up.

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Internal construction should be made of high grade stainless steel (minimum 22G) /Aluminium.External construction corrosion resistant sheet at least 1 mm thickness

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Internal temperature control: System should have temperature control range from +10 C to +8OC. Temperature control resolution should be better than 10 C. Cooling down time of max of 150 min on half load.

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External ambient temp should perform in ambient temp up to +430 C.

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Door System should lockable double doors with double pane with self-closing door for better safety,

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Safety System: a) System should have large and clear Digital displays for the set/run parameters. b) The system should have chart recorder to record temperature changes with battery backup.

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The system should have key operated set point for the added security Alarms. System should have audible/visual warnings for over-temperature under temperature and power failure with visual status reports on critical functions. System should have battery backup and connections for remote alarm contacts.

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Should have adjustments for uneven bases. The adjustments should be easy to use like rotating a screw at the legs in the base,

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Scratch resistance internal of the cabinet (stainless steel or aluminum)

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Should have 6-10 adjustable drawers of stainless steel of 22G

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Power input to be 220-240VAC, S0Hz fitted with Indian Plug.

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Voltage corrector/stabilizer of appropriate ratings meeting ISi specifications. (Input 160- 260V and output 220-240V and S0Hz)

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Certificate: Should be European CE or US FDA or BIS certified.

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Electrical Safety conforms to standards for electrical Safety.

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Item 25: Embryo Transfer Simulator

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Item Description

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The Simulator should be Anatomically accurate with female lower torso and base unit

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Should have a Sensorized Abdominal Insert.

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Should have Simulated Convex Probe, Syringe, Speculum and Portable Light.

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Should be integrated with a a real embryo transfer catheter.

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5 The system should be integrated with Laptop with pre-installed software with minimum 10 clinical cases preinstalled.

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The system should have a LCD monitor of Minimum 21.5 inches or more

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Lifetime Free Software Upgrades

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Should be European CE or US FDA or BIS certified

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Item 26: Ovum Pick Up Simulator

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Item Description

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The Simulator should be withHaptic feedback with Simulation of the deformation imposed by the needle on the soft tissues.

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The Simulator Should have a Simulation of follicle emptying and re-filling.

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Should have Scenarios based on real clinical images.

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Should have Monitoring of the procedure by a simulated Transvaginal Echographic monitor with Real time simulation of emptying and re-filling of the follicles.

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The system should be accompanied with real pick-up needle and a simulated transvaginal ultrasound probe and simulated aspiration pump pedal.

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The system should be accompanied with a Laptop PC with Pre installed software

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Should be IP67 certified.

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The system should have a LCD monitor of Minimum 21.5 inches or more

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Should be European CE or US FDA or BIS certified

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TECHNICAL SPECIFICATION FOR 3D-4D doppler High Resolution Ultrasound (USG) Machine

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SYSTEM OVERVIEW:

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System should be the latest "state of the art" fully digital' Ultrasound equipment capable of performing, OBS-GYN, Abdomen, Vascular, Small parts, Lightweight and maneuverable, High Resolution LCD/LED Display 21.5 inches or more, Touchscreen, 4 Active Probe Ports.Automatic optimization,Auto TGC , 3D Multiplanar Display,Realtime 4D -Should support feature for surface rendering with placement of render live to reduce artifacts. It should be able to continuously update render line P!acement with fetal movement during 4D Scans. - Should support feature for delineating clearly the outlines structures of Interest using a shadowing effect, allowing the operator to observe structure behind the directly visualized structure during fetal imaging. -Should support feature for showing the blood flow with a sense of depth while reducing blood overflow and indicating the vessel with sharp edges. -Should support feature for adjusting slice thickness on 3D or 4D images to increase contrast reduction and should be able to obtain any plane from a 3D or 4D volume by drawing a line, curve or trace through the structure -Should have the option to measure the number and volume of follicles automatically. --Should be able to automatically place callipers for fetal biometric measurements -Should support feature to assess the fetal station, provide objective measurements an progress of Labor. - Should support feature to measure fetal head progression, direction and rotation during Labor. - Should support feature to automatically obtain the recommended views of the fetal heart for fetal echocardiography. -Tomographic Ultrasound Imaging, HD-Flow. STIC, Anatomical M-Mode, Wide Sector (Max Angle), Coded Contrast Imaging, B-Flow, Battery Pack, Sleep Mode - Fast Wake, Probe Favorites, 3D Print File Export, Report Editor, On Board Archive including, Preview and Pre selection, Advanced Security Package, advanced software options such as Windows 10 loT, etc without any additional cost.

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The system should have the following modes: B-Mode (2D), conventional M-Mode with varying sweep rates, Anatomical M-Mode, PW Doppler with high PRF (PW), High PRF Doppler Mode,(TD)-Tissue Doppler mode, Color Flow Doppler Mode (CFM), Power Doppler Mode (PD), directional power Doppler,HD-Flow Doppler Mode (HD-Flow), and B -Flow (BF), B/Color/FW Doppler in simultaneous real time.Volume Mode:3D Static & 4 D Real Time on Convex and Intracavity probes & Matrix technology pobes should be compatible with the system

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System should have fully independent triplex multiple mode operation for extraordinary ease during Doppler examination,should be possible on all probes.

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21.5 inches or more in High Resolution LED Display with DVI interface, Resolution: Full HD 1920 x 1080 pixel, Image Size: 1136 x 786, Fully Articulating Monitor Arm, « Tilt angle: +30°/-90° + Rotate: +90°/-90°, » Horizontal Range of Motion: 250 mm (9.8 in),« Vertical Range of Motion: 100 'mm (3.9 in),Digital backlight and colour temperature adjustment settings available (eg. Dark, Light) and touch screen capable with option for volume rotation, light source adjustment, etc., capable of displaying 2D/3D/4D Ultrasound Images in real time & 4 Active universal Probe Ports

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Volume imaging, Multj- slice imaging with variable slice thickness and multiplanar imaging on all types of 3D and 4D modes.

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System should have facility for volume 3D/4D with Convex and option of taking 4D TV Probe in | near future.

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Should be capable of performing live 4D Imaging with Volume transducers. 4 D imaging should be possible in Gray scale, colour mode, harmonic mode. Instant rendering of MPR images should be possible that rival acquired 2D resolution. 3D/4D tool Obtain any plane from a 3D or 4D volume by simply drawing a line, curve, polyline or itrace through a structure. This valuable technology enables views of even irregularly shaped structures nol attainable in 2D imaging. Excellent approach for examination of complex structures with curvilinear or irreqular shapes. Benefit Reduces your manipulation of X-Y-Z Allows any slice in any plane - no longerlocked into orthognnaJ planes Ease of understanding of coronal plane when you simply ‘draw’ one.

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System should have 28,00,000 or more digital processing channels. Higher number of channels will be preferred

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Dynamic range should be 265 dB jor ‘more, with range adjustab\lny by selecting different Dynamic Contrast Curves. ngher dynamac range will be prvfevred

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A 2D imaging depth of at Minjmum Depth of Field: 1 cm (Zoom, probe dependent) Maximum Depth of Fweld 40 cm (probe dependent) More will be preferred.

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256 (8 bits) discrete gray /levals A

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Maximum colors in 24 bit

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20 acquisition frame rate more than 1500-2000 frames/sec, color Doppler frame rate more than 400/s

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Multiple focal imagmg

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Real time compounding with colour or power Doppler imaging

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Multiple frequency selection for better penetration and resolution for better tissue differentiation and better contrast resolutlon

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Post processing tools for annotation,measurement, correction of angle, baseline, sweep speed should be possible on stored images

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System should have multivariate Tissue Harmonic imaging facility including coded harmonics on all transducers. It should be able to operate with compound imaging and speckle reduction algorithm. System should have one touch tissue contrast resolution adjustment without altering the set pre-sets levels

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System should have real time compounding image tehnology with minimum 11 transmitted lines of sight. Real-time Compound Imaglng should operate in conjunction with Tissue Harmonic imaglng, volume modes, Panoramic imaging, and duplex Doppler, and in conjunction with speckle reduction imaging

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{High resolution algorithms for advanced speckle noise reduction, refined tissue pattern displays,and fine border definition. Should operate in 2D and 2D/CFI/Doppler mixed modes and with 3D and contrast agent imaging. This feature shall have operalor selectable settings and be capable of dlsplaying in side-by-side mode with non-speckle reduced image

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Should have trapezoidal imaging and steerable imaging for 2 D, color & Doppler with linear probe. Beam Steering should be possible with angles up to 30 Degree on linear probe.

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Panoramic / extended field of view imaging should be available on 2D mode on convex and linear 22 | transducers. This mode should build the extended field-of-view in a real-time manner, showing the image as it builds.

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One button automatic adjustment/optimization for 2D mode, color mode and Doppler mode.with auto correction of relevant fields of the 3D mode as well

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Incorporates advanced technology like coding excitation transmit technology and coded harmonics mode for imaging deeper areas for imaging obese patients will be prefered.

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The system should have a fast boot uptime less than 200 seconds when switch 'ON' from 'OFF'position, and also less than 20 second. from ‘STANDBY" position. Specify the system booting time, less will be preferred.

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System should have high capacity fans with automatic speed for system cooling.

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Year of introduction of the specific model- should be as latest possible,preferably should have been launched within 3 years.

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Unique user-friendly user interface for comfort and fast throughput.

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SYSTEM CONTROLS:

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System should have at least 45 automated and user programmable pré-sets/ (output power,signal processing and calculations).

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System should have facility to adjust 2D performance instantly for different patient types (Thin, 30 average, obese).

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The system shall display thumbnails on a clipboard with live gray mode while scanning to facilitate exams.

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Pan and zoom facillty with high resolution results in both live & frozen images. Higher zoom will be preferred. with HD-Zoom functionality up to maximum possible.

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Cine loop review facility in individual and mixed modes should be available.

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Post processing in Freeze mode (Dynamic Range adjustment, Color display on / off, Color / Doppler invert. Color / Doppler baseline adjustment, sweep speed, measurement, annotation and pictogram). Post processing of B-mode images with Speckle Reduction algorithm.

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Real-time automatic Doppler calculations on touch of a button. Should provide facility to apply automatic Doppler analysis retrospectively to frozen spectral data or date retrieved from Doppler scrolling. Possibility of manual Doppler trace

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System should have at least 8 callipers with depth information and extensive, customizable 36 measurement and report packages including Vascular, Abdominal, Small-Parts, Urology, Pediatrics, Ortho, Neurology, complete Obstetrics, multi-gestational Calculations, Gynecology, and Fetal Heart report packages.

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Callipers should have minimum precision of 0.1 mm, Small size callipers for measuring 5 mm

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Callipers of dynamically varying contrast compared to background. Delele last measurement option, curved linear distance measurement.

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Measurements (distance & area) should be possible in real time (non-frozen), frozen & on saved images as well.

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Facility to save reports along with patient data which can be retrieved later. Measured parameters must be printed directly in form of a report through laser printer.

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System should have facility of electronic biopsy guide and algorithm for clear needle visualization. The system should be capable of displaying biopsy lines (for all Transducers) while performing a fusion of B mode and color mode

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Speed & Volume Angle adjustment on volume Imaging

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Different render direction to view the volume image.

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Advanced tool for accurale quannflcatnon of irregular regions in 3 D & automatically calculates the number and volume of hypo-echoic structures to speed follicular assessments

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Ability to restrict firing of the probe to a particular slice thickness of the region of interest

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Advanced tool for selection of slice thickness out of complete volume dataset

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4D fetal Echo- 2D +COLOR+B flow, STIC + Power Doppler Mode + STIC + CFM Doppler Mode, * STIC + HD-Flow Mode" STIC + CRI STIC + CRI + CFM* STIC + CRI + PD STIC + CRI + HD-Flow= STIC + B-Flow STIC + multi-slice mode with cine movement.

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Advanced imaging mode for visualisation of hypo-echoic areas and get automatic precise volume followed with the measurements of each region and proper reporting.

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Simultaneous visualisation of 3 planes and Realtime 4D guide the needle to the lesion

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Additional Software- rélated to follicle, Biometry Advanced 4D , Render should be quoted as standard, part of the Scope of supply Transforming Nuchal Thickness measurement with automatlon within fraction of seconds.for the fast and accurate scanning supporting sonographers or radiologist to finish their scan within short time

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Should have auto 3D/ 4D rendering as well to get the best reproduction of 3D image in fraction of second with one touch

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Advanced Spatic Temporal Imaqe correlation with STIC & Annatomical-M mode for the diagnoses of atrial and ventricle synchronisation/ disfunctionality of the Fetal heart. Automated sonograph based technology helps streamline the acquisition of volumetric images of the fetal heart, displaying all eight recommended views with two steps after accusation of volume data set

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PHYSICAL DIMENSIONS

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The equipment should be a room based wheeled unit with integrated brake, footrest, transducer, cable and gel bottle holder, and with hydraulIc height adjustment facility for control panel and monitor independently. Transducer and gel bottle holders should be provided from both sides of the keyboard for the user-friendliness of the machine.

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21.5 inches or more in High Resolution LCD LED Display with DVI interface, Resolution: Full HD 1920 X 1080 pixel. FuIIy Articulating Monitor Arm « Tilt angle: +30°/-90° . Rotate: +90°/-90

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Extra Light Innovative user interface with high resolution 10.1 in LCD touch panel & system should have a full- size, Alphanumeric, Keyboard with interactive backlighting. The keyboard could be floating or fixed type with range of rotation and adjustable height available. Floating will be preferred.

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Integrated recording keys for remote control of up to 4 Peripherals or DICOM devices, one dedicated DVD recording key.

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The system shall have 4 universal probe ports easy to access location with electronic switching facility. 4 Active universal Probe Ports

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IMAGE STORAGE, DOCUMENTATION DEVICES & CONNECTIVITY ISSUES

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Must allow digital storage of gray scale as well as color images (both frozen & cine loops). Facxlny of reviewing and exporting in different formats.

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System shall support the ability to store digital raw data that allows optimizing imaging 58 parameters such as B Gain, TGC, Color Gain, Dynamic Range, Speckle Reduction levels, Doppler Gain, Doppler Base Liné on image recalled from the image archive

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The system should have on board storage facility for at least 500 GB.The hard drive should be inbuilt. Cine Features: 1. Dual/Quad image CINE Display 2. CINE Gauge and CINE image number display 3. CINE Review Loop + Selectable CINE Sequence for CINE Review (by Start Frame and End Frame) 4. Side Change in dual CINE Mode * Measurements (Calculations & Annotations on CINE Length:

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The system shall provide the ability to sort images stored on board based on patient name, exam date, patient ID and exam types. Patient directory should show network status as print status, archive status, commit status and export to DVD status, Integrated Software DVR + Digital recordings "One drive for data export and recording + DVD Formats: DVD+R, -R, +RW, -RW for recording, DVD and CD support for data export « USB support: FAT32 compatibility

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Possibility to modify / edit patient data during and after exam has been stored and saved

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Must have an integrated CD /DVD writing- burning facility and it could be viewed on any ordinary PC. Machine must have capability to write CD/DVD separately of a previous patient during scanning to save time. Should be able to archive data from previously stored CD/DVD. DVD/CD drive to store / retrieve images in different formats (TIFF/AJPG / AVI / DICOM) /. Patient reports

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System should be DICOM (higher version) ready (Storing Transfer, Printing)

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USB PORT: minimum 4 USB ports in machine and must be providing with USB memory stick transfer images.

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System should be easily intergraded in hospital PACS without any extra cost,

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Transducers should be of broadband technology for extreme high-resolution images. Please specify model number, footprint, bandwidth, imaging frequency, Doppler frequency, FOV and weight of each transducer. Light weighted transducers with flexible cables will be preferred. Biopsy guides should allow various size needles

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Multifrequency 2D convex transducer: Wideband Convex Probe -Applications Abdomen, Obstetrics, Gynecology Maximum Bandwidth 2 — 5 MHz or better. Biopsy Guide Avallable Multi- Angle, with reusable bracket

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Broadband 4D convex probe light weight will be preferred. Wideband Convex Volume Probe Applications Abdomen, Obstetrics, Gynecology, Pediatrics Maximum Bandwidth 2 — 8 MHz or better. Biopsy Guide Available Multi-Angle, with reusable bracket

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Wideband 3D/4D capable Transvaginal Volume Probe with Biopsy guide attachment. Applications Obstetrics, Gynecology, Maximum Bandwidth 3- 9. MHz or better

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Wideband Matrix Linear Probe Applications Small Parts, Peripheral Vascular, Pediatrics MSK, Breast Maximum Bandwidth 4-13 MHz or better.

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ACCESSORIES

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B/W thermal printer of Iatest mcdel (wnh CE / FDA/ BIS mark) for image printouts. Please specification the brand,model and specification details.

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UPS for backup

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GENERAL INSTRUCITONS TO VENDORS:

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All information in the tender document must be supported in the product data sheet.

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Compliance statement sheet must quole page number/s as it appears in the product data sheet enclosed by the vendor.

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Supplier should be able to demonstrate its quoted model when and where required along with quality control programme for system performance

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Supplier must attach the list of installation in leading Diagnostics centres hosplta[s orin institutions inside India (at least 100)

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System should be ISO, CE / FDA /BIS Lemfled

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Minimum 5 years warramy + 5 years CMC

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Note: All Tenders should quote item/items with following approved standards and shelf life:-

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Tenderer must enclosed copy of CE (European)/USFDA/ DGCI/WHO GMP/BIS/ISI/CDSCO, which so ever applicable for requested consumable items.

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Manufacturers/suppliers should have ISO certification for quality standards (i.e. 9001:2015).

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Substandard and rejected items must be replaced within 15 days times by the approved Supplier Agency, if any such intimation received from AIIMS bhopal in writing.

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General Specifications for all purpose latest C-Arm Image Intensifier System Qty-(01)

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The offers are invited in two bid systems (Technical bid + Financial bid) for the purchase of latest Mobile C arm Image Intensifier system. The C-arm unit should be state of the art, currently under production capable of sleek movements for Multipurpose applications. Please mention the year of launch. The C -Arm Unit should allow unobstructed positioning and ease of operation, should have the following features.

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Mechanical motion requirements for C-Arm:

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i Motorized vertical travel: 450 mm or more

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ii Pivotal rotation/ swivel range: plus/- 12.5 degree or more

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iii Arc Orbital movement: 120° ( -30° to + 90°1or better

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iv Horizontal Movement should be: 200mm or better

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V Source to Image Intensifier distance (SID Range): 960mm or better

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vi Free space between lnage Intensifier and X-Ray Tube: 760mm or better

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vii Rotation of C-arm: +/-180° or more 630mm or better (adequate to encircle OT Table & bulky patient)

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viii Depth/Radius of C-arm should be: 630mm or better (adequate to encircle OT table & bulky patient)

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The C-arm should also have Foot Lock facility at control Panel to immobilize the unit (Foot brake directly applies on wheels for effective braking). It should have mechanical Locks for all the movements of C-Arm

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Imaging Section: (Image Intensifier & TV Camera) The Image Intensifier should have triple field 9"/6"/4.5" input diameter with 10:1, 100 lines X-Ray Grid. TV Camera should with compact . CCD/CMOS camera oh high no of pixel (752 × 582 pixels) or more . Modular trolley with 2 Nos. 19” flicker LCD Monitors with monitor’s foldable facility.The System should have facility to rotate the image continuously Modular Trolley with 2 Nos. 19" flicker free LCD Monitors with monitor's foldable facility The System should have facility to rotate the image continuously.

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X ray Generator & Control Panel: The X ray generator should high frequency of 40KHz with maximum 3.5KW output. X ray generator should be capable of operating between 40 KV to 110 KV The X Ray generator should support mA in the range of 0.1 to 3 mA for continuous Fluoroscopy, (""'The X Ray Tube should have focal spot of 0.6mm2 for Fluoroscopy and 1.5mm2 for Radiography. The Anode heat storage should be 40KJ or more. The Boosted/High Definition Fluoro should be 7.5 mA or better. The Snapshot mode Fluoro should be 8mA or better The System should have Pulsed fluoroscopy with l,2PPS. The Radiography mAs should be 200mAs or better. The Radiography mA should be up to 80mA. , X-Ray exposure should be initiated through the Foot Switch & Hand-held Switch The C-arm system should have Digital Control Panel with 10-inch Full Touch Screen display as standard. The system should have facility of Image Rotation, Averaging, Edge Enhancement, Image Invert, Image Flip & Image Save from Control Panel The system should have a facility to select KV & mA (Manual/ Auto mode) The Display of live Fluoro image should be available at the Control Panel for fast & precise positioning. The System should have access of Laser Aimer ON/OFF facility at Control Panel Digital Image Rotation (CW/CCW) from Control Panel The Control Panel should have the facility of Display of all Fluoroscopic and Radiographic Parameters Viz. KV, mA, time and operating mode, Magnification, Real-time Tube Head Temperature Indicator with Bar Graph. A five minutes cumulative timer with buzzer should be available.

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X-Ray exposure should be initiated through the Foot Switch & Hand-held Switch

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The C-arm system should have Digital Control Panel with 10-inch Full Touch Screen display as standard.

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The system should have facility of Image Rotation, Averaging, Edge Enhancement, Image Invert, Image Flip & Image Save from Control Panel

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The system should have a facility to select KV & mA (Manual/ Auto mode)

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The Display of live Fluoro image should be available at the Control Panel for fast & precise positioning. The System should have access of Laser Aimer ON/OFF facility at Control Panel

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Digital Image Rotation (CW/CCW) from Control Panel

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The Control Panel should have the facility of Display of all Fluoroscopic and Radiographic Parameters Viz. KV, mA, time and operating mode, Magnification, Real-time Tube Head Temperature Indicator with Bar Graph.

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A five minutes cumulative timer with buzzer should be available.

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Emergency Stop switch for manual shut-off.

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Digital Imaging Processing

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The C-arm·unit should incorporate PC based Image memory with the standard Features as mentioned below:

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• System should have capability to display (measured or calculated) the Patient's Dose Rate & Accumulative dose.

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• New Patient Registration with Patient details, Procedure details, Doctors Name, Date and Time.

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• Display of Information like Patient ID, Patient name, Patient Age, Operating modes, Rotation, kV& mA value

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display, Hospital Name.

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• Real Time Brightness and Contrast adjustments for improved image quality.

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• Permanent image storage capacity of 2,00,000 images.

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• Image rotation (+/-180 degree) clockwise and anti-clockwise atldegree step.

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• Image orientation: Left/ Right (Horizontal Flip) and Top/ Bottom (Vertical Flip).

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• Negative Images (grey level invert).

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• Image averaging for Noise reduction (2, 4, 6, 8, 12, and 16).

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• Real-time Edge enhancement.

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• Manual Save and Auto save facility of Images..

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• Reference Monitor - Transfer the image from Live to Reference Screen.

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• Multiple Image View on reference monitor: Single, QUAD, 9 images and 16 images

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• Cine loop acquisition: 1,2,4,8,15,25 frames per second

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• Cine-loop Display (Play, Pause and Stop) and Frame by frame review.

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• Quick exploration of stored images from Search Patient.

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• Thumbnail view for Images and Cine loop.

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• Cine-loop Display (Play, Pause and Stop) and Frame by frame review in Reference monitor.

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• Image post processing filters on saved images (Sharpening, Mean Filter and Median Filter)

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• Standard Edge Detection Filters.

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• Image Zoom in, Zoom out and Pan

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• Measurements & Annotation facility

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Data Documentation

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• Software should have facility to generate the Patient Report

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• USB Image Export Facility

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Image Acquisition & Storage System (PC)

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• Intel Core(TM) i3-4150 CPU @ 3.50 GHz

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• Minimum 4 GB RAM

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• 64-bit Operating System, Windows 7 Professional

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• DVD Writer

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• Spill-proof Keyboard with integrated touchpad

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Power Requirement

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• The System should have Isolation Transformer to safeguards the equipment from power surge, Spike, fluctuation & prevent from electric shocks.

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• Power input to be 230Volts + 10% Ac, 50 HZ fitted with 15-amp plug.

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Essential Accessories:

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The complete functional system must be quoted with dual channel Laser light preferably on Image Intensifier end to reduce the X-ray dose,

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• Light weight aprons (5 No),

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• Suitable UPS for PC with back-up of 15 mins at least

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NOTE:

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The quoted equipment should have BIS or US FDA or European CE with four digit notified body and AERB type approval and equipment should comply with AERB guidelines for leakage radiation & Table top dose

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Manufacturing firm should be ISO 13485 approved.

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Technical Specification for the Desktops at IVF Lab

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OS: Winsdows 10 Pro (OFFICIAL VERSION) and above, Intel Core i5 Processor or 8 GB RAM1 TB GB available hard disk space, DirectX 9 graphics device with WDDM 1.0 or higher driver, 1 Ethernet Port, 3 SPARE usb Drive

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Anaesthesia Workstation

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Technical Specification

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Compact and modular, three gas Anesthesia workstation with an integrated ventilator for adult to infants and integrated airway monitor for airway pressures and volume.

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The Machine should be suitable for low and minimal flow anesthesia application with compliance compensation of breathing circuit, fresh gas flow compensation/ decoupling.

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Anesthesia machine should have minimum 60 min. battery backup.

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Manufacturer should have own registered office/own registered service centre/100% Subsidiary company in India/Distributorship in india. Necessary document in the name of manufacturer/100% subsidiary/Authorised Distributorship company like GST Registration / Trade License to be submitted along with bid;

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Gas Delivery System

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Should have pin index yokes one for oxygen and one nitrous oxide besides separate connection for central gas supply for oxygen, nitrous oxide and air.

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The machine should have pressure gauges for cylinders and central supply lines visible from the front of anesthesia machine. The gas connections should be non-interchangeable.

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Automatic cutoff of N2O / oxygen pressure failure.

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Hypoxic guard for liner regulation of minimum oxygen concentration at 25% volume and must ensure a minimum oxygen flow of 200ml at low fresh gas flow setting even below total 500 ml fresh gas flow.

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Audio-visual oxygen failure alarm.

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Emergency oxygen flush at 35-70L/min bypassing the vaporizer

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Should have O2 monitoring with paramagnetic/Galvanic fuel cell technology and should be covered under warranty for 5years and thereafter under CMC. Anaethesia gas monitoring on the Ventilator Screen

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Should have Auxiliary O2 flow meter.

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Multi gas module with paramagnetic O2 Capnography, agent id and Mac values to be monitored displayed along with other features

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Flow meter

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Dual cascade type flow meter tubes for oxygen, N2O & Air (Or electronic gas mixing). Range 0ml /min to 10lit/min.

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Calibrated in multiple scales. Dual tube for air 0 ml to 1L/min and 1 L/Min to 10 L/Min

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Vaporizer

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Machine should have facility to mount two quick mount type selectatec vaporizer for easy interchangeability and safety

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Should be provided with a temperature / pressure compensated and flow independent vaporizer for Isoflourane

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Vaporizer should have extended delivery range with standard marking.

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The vaporizer design should be with one time life time calibrated.

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Breathing System

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Should have semi closed circle absorber system. Initial Soda Lime requirement of the absorber capacity to be supplied as standard.

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Should have adjustable pressure relief valve from 0 to 60m bar.

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Should have change over from spontaneous to Bag ventilation with single step and/or a confirmation message on ventilator screen

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Should have an external fresh gas outlet for connecting Magill or Bain’s circuit.

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It should have CO2 bypass feature.

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Anesthesia Ventilator

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Electronically controlled electrically driven / pneumatically driven ventilator

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Should not require changing of bellows for adult & infants.

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Modes: Volume controlled, manual / spont, pressure controlled mode,pressure support (or SIMV with PS), SIMV,SMMV,PRVC

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Tidal volume : 10 ~ 1500ml

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PEEP : 4-20 mbar

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Breathing Frequency : 4 to 100 BPM

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IE Ratio : 2:1 to 1:3

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Inspiratory pause: 5 – 50% of Ti

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Flow : 0 to 100 L/min.

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Pressure limiting (Pmax) : 10 – 70 cm H2O

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Should automatically compensate for compliance of breathing system

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Airway Monitoring

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Integrated monitor should be min 10" or more color display/EL) for electronic monitoring and display of following set and measured values

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Expiratory Tidal Volume, Expiratory Minute volume, PEEP, Peak and Mean and Plateau

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airway pressure, Frequency, Waveform and loop display for Airway pressure, flow and volume on Ventilator Screen.

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Alarm limits and alarms

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Adjustable high / low limits with audio and visual alarms for the following:-

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Minute volume, airway pressure (incl stenosis and disconnect), Insp oxygen concentration, audio power supply fail alarm, low driving gas pressure, low battery Apnoea alarm

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Machine should have RS 232/USB connectivity port.

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Monitor (ECG, SpO2, NIBP, Dual Temp, Resp )

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Should be suitable for adult, paediatric and neonatal patients monitoring

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Should have minimum 6 channels of waveforms with minimum 15” color touch screen display with vertical and horizontal cursors.

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Battery backup for 60 minutes should be provided through internal batteries or UPS

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Should have automatic graphic and tabular trending of all monitored parameters as standard for at least 24 hours.

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Should have minimum ECG, NIBP, SpO2 (Masimo/Nellcor technology), 2 Temp with OEM Complaince

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Should have ST segment analysis and arrhythmia detection including life threatening arrhythmias such as V. TACH, ASYST, V. FIB as standard features.

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Should have manual as well as automatic scaling of screen format.

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Should have user selectable parameter priority and colour selection for parameter on screen.

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Monitor should have ESU and Defib protection feature

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The quoted model (Both Anaesthesia and Monitor) should be European CE with four digit notified body number or US FDA or BIS approved for the quoted model and certificate to be submitted.

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Anaesthesia machine with ventilator and patient monitor should be compatible to each other

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Scope for supply with each machine:- (As per BOQ)

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Anaesthesia Machine with Integrated ventilator without vaporizer

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Isoflurane vaporizer

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ECG, SpO2, NIBP, Dual Temp, Resp (Combined or separate or integrated)

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2IBP if separate

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BIS/Entropy/Anaesthesia depth monitoring

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Adult autoclavable patient tubing (Silicon)

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Paediatric autoclavable patient tubing (Silicon)

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5 lead ECG cable

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SpO2 finger sensor with extension cable (adult)

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SpO2 finger sensor with extension cable (Paeds)

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SpO2 finger sensor with extension cable (Infant)

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Skin Temperature probe

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Rectal / Esophageal temperature probe

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NIBP Hose

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Adult cuffs

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Paeds cuffs

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Infant cuffs

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Large Adult cuff

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IBP reusable cable

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Disposable IBP transducers

Quantity10

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Sample lines for EtCO2

Quantity10

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System shall be intergraded system with high stability, upgradability, data storage, retrieval, display analysis and printing.

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Transport monitor should be compact design, small in size ≤ 1.5 KG for better portability.

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Monitor should support optoion for handle/docking for users to carry/hook on trolley bed.

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Monitor should be able to used as a standalone device, or be used as a module for modular monitor from the same manufacturer.

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Support up to 6 parameters measurements by own simultaneously.

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Support adding parameter base on clinical needs by using Plug-in-out module. Module can be used among all modular monitors from the same manufacturer.

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Should provide parameter, alarm, and monitor configuration save and transfer function, the clients can use a USB drive to transfer the configuration from one monitor to another monitor that needs the same settings without having to set the configurations item by item again.

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The monitor should be able to work from 54 kpa to 105 kpa

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Should have IPX1 Certified

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The monitor should have cooling system free of fan to eliminate noise and potential infection risk.

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Should be supplied with Li battery back up of Minmum 2 hours

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DISPLAY

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1. Monitor should be color TFT LCD screen, with screen size not less than 5.5 inches, and minimum resolution 1280*720 pixels.

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3. The monitor should be able to adjust brightness automatically to allow readings be observed clearly in all kinds of light environments.

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4. Support different display mode: standard mode and high resolution display mode for more information.

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6. Option for most frequently used quick keys for users to choose and put them on quick keys sections of main screen, allowing access to certain functions or displays without entering multi-layer menu.

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7. The monitor should support up to 4 channels of waveform display, and the waveform color and position are adjustable.

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8. The monitor switched between minimum of 5 display interfaces including Standard Screen, 12 leads ECG, OxyCRG, Dynamic Trend, Big Font, etc

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9. The touchscreen shall support auto lock to avoid mis-operation, cleaning and disinfection purpose for a configurable period of time, from 1min to permanent. Also support manual unlock.

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10. Users shall be able to freeze the waveforms on the screen for reviewing data from 100s before pressing the button.

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11. Monitor shall provide following specific working modes: Outdoor mode, Standby, Night, Privacy modes.

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PARAMETERS

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Monitors shall be able to measure following parameters simultaneously:

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1. 3/5/6 lead diagnostic ECG/Respiration with heart rate, ST segment analysis with 27 or more arrhythmia detection

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2. Can be upgradable to 12-Lead Diagnostic ECG

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3. Pulse Oximetry – SPO2 (Motion tolerant and waveform)

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4. Temperature - Rectal or Skin Temperature

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5. Respiration (Can be obtained from ECG, SPO2, or EtCO2 as source)

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6. Non-Invasive Blood Pressure (NIBP)

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The monitor should have capability to upgrade to following:

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1. EtCO2 (Mainstream/Sidestream/Microflow)

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2. NIBP (Suntech)

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3. SpO2 (Masimo/Nellcor)

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ECG Monitoring

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1. Display of 3/5 and 12 lead diagnostic ECG

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2. Monitor shall simultaneously display one or two channels of ECG at any given time at user's option

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3. Frequency range: 05 to 120Hz or better

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4. Shall have built in filters for AC interference, drift, and electro surgical interference. Defibrillation and high frequency electrosurgical interference protection.

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5. Heart Rate Range: 15 to 300 bpm or better

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6. Should have ST segment analysis and ST graphics

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7. Shall have pacing detection and defibrillator discharge protection.

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8. ST mapping and 12 lead ECG monitoring with analysis

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11. Shall have QT/QTc, △QTc analysis

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12. Shall able to support 27 types of Arrythymia analysis

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13. Monitor should provide multiple leads analysis feature, heart rate can be accurately monitored in the event of individual lead interference

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14. There should be alarms and graphical guide to help users to identify when leads off

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SpO2 Monitoring

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1. Shall be motion tolerant

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2. Shall provide oxygen saturation percentage level, pleth waveform and pulse rate in beats per minute.

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3. Measuring range: 0 –100% in 1% Resolution

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4. Shall provide for visual and audible alarms for high/low saturation and pulse rate

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5. Accuracy: +/- 3%

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6. Pulse rate counting range: 30-300bpm

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7. Monitor shall have Motion artifact rejection in SPO2 measurement with perfusion index.

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8. Module shall be capable of retaining alarm settings for patient transport

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9. Should have optional Masimo/Nellcor SPO2 upgradibility by using docking station

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10. Support obtain respiration rate from SpO2 sensor

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11. Analog SpO2 (Same Manufacturer) as standby with adult sensor

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NIBP Monitoring

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1. Measuring method: Oscillometric

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2. 4 Measuring Modes: Manual and Automatic with selected intervals, STAT and Sequence

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3. Accuracy: +/- 4mmHg

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4. Module shall trigger an in-operative condition alarm if a static or overpressure is detected

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5. Shall provide venipuncture assistant by using BP cuff

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Temperature Monitoring

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1. Range 0.0°C to 50.0°C / 32°F to 122°F shall be provided

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2. Monitor shall be capable of having a minimum of two temperature channels

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3. Accuracy ±0.1°C / ±1°F

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4. Shall be able to monitor both Core and Surface temperatures simultaneously

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EtCO2:

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1. Measurement method- Main Stream, Side stream or Micro flow- using infrared absorption technology

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2. Measurement parameter should include EtCO2, FiCO2 , CO2 waveform and awRR

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3. EtCO2/FiCO2 measurement range: 0mmHg ~ 140mmHg with accuracy of 0.1% or 1mmHg

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4. awRR range: 0~150 bpm with accuracy of ±1 bpm

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5. Main stream adapter shall be light weight – Less than 20G, shock resistant and have a quick warm up time

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Clinical Assistive Applications:

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1. Deleted

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2.Deleted

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3. Calculation - to provide calculation for: Hemodynamic calculation, oxygenation calculation, ventilation calculation, drug calculation, renal function calculation

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Storage

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1. Full disclosure of 72 hours or more

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2. Support transfer of data for discharged patient

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3. Support review of 48 hours OxyCRG to provide trend curves and a compression waveform

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4. Ability to display beat-to-beat event trends for all monitored parameters at least 24 hrs with capability to provide event review

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5. Support review of alarm events and filter results base on users preference.

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Alarms

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1. Advisory & critical warning alarms both in continuous & repetitive audible & visual form

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2. high & low alarm settable for all parameters

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3. Adult & Pediatric & Neonate capability

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4. Ability to pause & silence

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General Conditions

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The unit shall operate on the power supply of 230±10% 50 Hz single phases.

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Each unit shall be supplied with an instruction manual and a service manual in English.

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All standard accessories shall be supplied including relevant software. Other relevant optional accessories shall also be quoted separately.

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Regular training for end users & Bio Medical Engineers shall be provided

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The bidder must arrange for the equipment to be installed and commissioned by certified or qualified personnel: any prerequisites for installation to be communicated to the purchaser in advance.

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Certifications:

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Bidder shall furnish the documentary evidence to demonstrate that the good it offers meet the following usage requirement 1. ISO certificate for good manufacturing practise 2. US FDA/European CE certificate from 4 digit notified body/BIS certified

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Bidder shall be also responsible for supply, installation, testing and commissioning of OT Table and OT light.The specification of OT and OT light as follows

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Gynae OT Table

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Technical Specification

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Multipurpose electro hydraulic with manual/elecrtical override mobile Table with divided leg section suitable for all Gynaecological surgical procedures, complete with 5 cm mattress and corded handset.

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General operating table features:

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Full-length radio-translucent top.

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4 or 5 sections tabletop, which should be made of a special scratch resistant, hardwearing and easy to clean material. Base and entire column cover to be made of 100% stainless steel alloy and stainless steel.

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Removable head and leg sections to suit different applications.

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Battery powered, with facility for connection to mains electricity for immediate use. Battery Exhaustion protection and low battery warning via an audible „beep‟/display indicator should be available.

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Table should not have a thread/sharp edge for ensuring proper cleaning and user safety.

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Mattress should be of high quality that spans tabletop break for improved patient support. Its depth should be 50mm. Mattress must be Latex free.

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The robust handset should offer minimum 8 controls namely Trendelenburg and Reverse Trendelenburg , Lateral Tilt, Zero position, Longitudinal slide and Height functions.

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Brakes, 4 nos. Wheels.

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Table should have a narrow T-shaped base allowing optimum access and greater stability.

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The table top should not be fitted with transverse members casting shadows on the X-ray images except for the release brackets for adjustment on either side.

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The Table should be operated by the following operating elements: corded hand control, Manual override panel with manual override facility / electrical override facility.

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There should be „U‟ cut compatible for Gynae surgery

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Electrical specification:

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Special-design, maintenance-free rechargeable batteries with back up of one hour

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Recharging of the batteries and supply of the operating table by means of a mains cord Nominal mains voltage (selectable) 220/230-240V AC via mains cord with inbuilt stabilizer

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Technical Data:

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Length : 1900 mm or more

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Width: 500 mm or more

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Minimum height (without mattress): 700 mm.

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Maximum Height (without mattress): 1000 mm

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Maximum lateral tilt: 20-30 deg. (either side)

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Trendelenburg: atleast 25 deg.

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Reverse Trendelenburg : atleast 25 deg

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Head section adjustment : ±40-45 deg.

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Leg section adjustment: +20 deg or more to -90 deg or more.

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Cranial & caudal traversing: 200-300 mm. It should be operated with remote control.

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Back section adjustment: (-35 to +75) deg.

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Maximum patient weight: 180 kg or more in all positions.

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Accessories

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Arm board - 2

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Lithotomy leg holders “Geopel type” (adult and paediatric)-1set each

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Body strap- 3

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Anaesthesia screen with clamps- 2

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Side supports with clamps – 2

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Knee crutches with clamps - 2

Quantity-

Rate-

Amount -

Clamp, rotary- 4 pc

Quantity-

Rate-

Amount -

Clamp, circular - 4 pc

Quantity-

Rate-

Amount -

Accessories stand, mobile on castors- 1 pc

Quantity-

Rate-

Amount -

Infusion rod with clamp

Quantity-

Rate-

Amount -

Drain Tray

Quantity-

Rate-

Amount -

Standards

Quantity-

Rate-

Amount -

Should be BIS certified for the quoted model OR should meet IEC 60601-1, IEC 60601-1-2 & IEC 60601-2-46 standards and should submit valid test report for the quoted model from NABL accredited laboratory/ from the labs in their country of origin in case of foreign manufacturer

Quantity-

Rate-

Amount -

Manufacturer should be ISO 13485 certified

Quantity-

Rate-

Amount -

Power Supply

Quantity-

Rate-

Amount -

Power input to be 220-240VAC, 50Hz fitted with Indian plug

Quantity-

Rate-

Amount -

Quantity-

Rate-

Amount -

OT LIGHT

Quantity-

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Amount -

OT Light – LED

Quantity-

Rate-

Amount -

Operating Room Surgical Lighting System should provide an ideal combination of brightness, maneuverability, and shadowless without sacrificing color accuracy through a consistent LED technology. The OT light should be ceiling mounted double dome high performance OT light. Such Lighting System should have the following technical specifications:

Quantity-

Rate-

Amount -

Number of Light heads : Two per suspension

Quantity-

Rate-

Amount -

Color Temperature range: 3800k-5000 (±10 %)- Variable color temperature.

Quantity-

Rate-

Amount -

Field Size Diameter : 20 to 28cm (+/- 10%)

Quantity-

Rate-

Amount -

Colour Rendering Index : 95 or more

Quantity-

Rate-

Amount -

Working Range : 750 to 1100mm (+/- 10%)

Quantity-

Rate-

Amount -

Illumination Level : illumination by each dome 160000Lux at 1 m

Quantity-

Rate-

Amount -

Controls : Control Panel (wall and on dome)

Quantity-

Rate-

Amount -

Rotation : 330- 360 degrees

Quantity-

Rate-

Amount -

Sterilizable Handle : 02Nos.

Quantity-

Rate-

Amount -

Mounting Type : Ceiling

Quantity-

Rate-

Amount -

Supply Voltage : 230 VAC 50 Hz

Quantity-

Rate-

Amount -

Bulb Type : LED

Quantity-

Rate-

Amount -

Dimming Range : 50% - 100% or 30% to 80%

Quantity-

Rate-

Amount -

Operating/Storage Humidity : 10 – 95%

Quantity-

Rate-

Amount -

Life of Light Source : 40,000 Hrs.There should be built in digital counter on the control panel to show the number of hours the light has worked.

Quantity-

Rate-

Amount -

Should have provision to mount the camera in one dome.

Quantity-

Rate-

Amount -

The dome and suspension should be sealed and dust proof

Quantity-

Rate-

Amount -

The light dome shall be compatible for laminar airflow

Quantity-

Rate-

Amount -

Should meet IEC 60601-1, IEC 60601-1-2 & IEC 60601-2-41 standards and should submit valid test report for the quoted model from NABL accredited laboratory/ from labs in their country of origin in case of foreign manufacture

Quantity-

Rate-

Amount -

Manufacturer should be ISO 13485 certified.

Quantity-

Rate-

Amount -

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