RequiredExperience with Government
RequiredAnnual Turnover
RequiredCertificate (Requested in ATC)
RequiredOEM Authorization Certificate
RequiredOEM Annual Turnover Bid to RA enabled No Holter With Monitor For Analysis ( 2 pieces ) ( Under PAC ) Make spacelabshealthcare Model spacelabshealthcarelifecardcf12 Technical Specifications * As per GeM Category Specification Specification Specification Name Values Bid Requirement (Allowed Values) GENERAL FEATURES Type Worn on a strap across * 1/6 the chest Clinical purpose A type of portable ambulatory electrocardiography device used for cardiac monitoring through recording the (ECG) electrocardiograph of heart * Patient category Adults Adults PRODUCT FUNCTIONAL FEATURES Number of Channels 12 12 Number of Leads 10 10 Analyzing various arrhythmias like ventricular ectopics
Requiredsupraventricular ectopics
Requiredventricular tachycardia
Requiredventricular fibrillation
Requiredsupraventricular tachycardia
Requiredatrial fibrillation
Requiredsinus pause Yes * Full disclosure of ECG with different Color coding for VE
RequiredSVE and PAUSES Yes * Hourly count menu
Requiredwith minimum two scan Yes * Minimum of 20 templates editing to analyse VE
RequiredSVE
RequiredV- RUN
RequiredSV-RUN
RequiredPAUSE
RequiredST
Requiredetc Yes * Atrial fibrillation/Flutter analysis Yes * Heart rate variability (HRV) analysis Yes * SAECG-Late potential analysis No No Pace Maker auto detection and analysis Yes * 12 Lead ST Scan Yes * QT analysis with validation Yes * To print ECG strips from any part of Holter recording Yes * T Wave altemans No No 2/6 Facility for electronic compact technique for Flash card/USB Cable Yes * Should be able to edit and reclassify beats and arrhythmias Yes * Should be able to re- edit individual form classes Yes * Should be able to consolidate individual form classes Yes * Should have scroll function for the over view (super page of the ECG) Yes * LED indication for data storage and device status Yes * Sleep apnea analysis Yes Yes RECORDER CONFIGURATION Recorder should be minimum 3 channel ECG for recording data duration 24 Hrs 24 Hrs Removable storage memory card CF Card CF Card digital recorder with removable storage media such CF card/SDHC Card/USB Cable Yes * Memory storage capacity of Card 128MB 128MB Should save 24 or 48 hours of ECG into flash memory card/inbuilt memory Yes * Saved data should be read using integrated reading device Yes * Number of Lead cables 10 10 Integrated Lead Wire length (Cm) 150 150 Compatibility with Alkaline battery Works on 2 Nos 1.5V (AA) Alkaline batteries * Pace maker spike detection Minimum 512 samples/sec/Channel * 3/6 Recording and Storage Minimum 128 samples/sec/Channel * VLP Minimum 1000 samples/sec/Channel * PC SYSTEM & SOFTWARE REQUIREMENTS PC System Pentium latest
Requiredcompatible Intel chipset
Requiredmemory 4GB RAM DDR
Required500GB Hard drive Pentium latest
Requiredcompatible Intel chipset
Requiredmemory 4GB RAM DDR
Required500GB Hard drive Software capable of working with windows XP/Windows 7/Windows 8/Windows 10 Yes * Software should Include "(a) Holter analysis b) Trends c) Strips d) Page e) QT Analysis f) Shape g) Event review h) Episode review i) Final Report j) TWA alterns analysis" * Monitor 17 inch colour * Real time average complexes Yes * Real time ST analysis Yes * The system should have facility to do re – analysis of stored ECG by changing line measurement point title ST and J Yes * The system should present comprehensive final report on minute by minute record of ST segment trend Yes * The system should have automatic arythmia detection Yes * ST profile
RequiredST elevation
RequiredST depression
RequiredHeart rate
RequiredMets
RequiredNIBP
RequiredST index should be able to be clearly analyze Yes * PDF generation and Email facility Yes * Printer Ink-jet Ink-jet UPS Yes * REPORT FORMAT Format for reporting Indications
Requiredsymptoms
Requiredtime
Requireddiagnosis
Requirednotes and conclusions with space for personnel and physician electronic signature. Format for Examination summery should include Quality of recording
Requiredbaseline rhythm
Requiredmin and max heart rate
RequiredVE
RequiredSVE
RequiredVT
RequiredSVT
RequiredBlocks and Pauses * Report format should include covering page
Requiredarrhythmia analysis report
RequiredST segment analysis
Requiredautomatically and manually selected ECG strips Yes * ST segment analysis should be available for all selected channels Yes * PACKING MODE All the items should be placed in suitable Carton box/plastic case/box with thermocol packing in such a way that there will be no transit damage during transportation & usage Yes * CERTIFICATIONS & REPORTS Submission of Test Report from OEM complying the declared specification at the time of supply YES * Product certification US-FDA US-FDA Certificate No K110001 * Certificate Date jun 14 2011 * Certificate issuring authority Us FDA * Four digit number of notified body If product is EU-CE certified 123 * Submission of all the certifications and test reports to the buyer along with supplies on demand Yes * WARRANTY & MAINTENANCE Comprehensive maintenance warranty 5 * 5/6 (Year) Contact details of manufacturer
Requiredsupplier and local service agent to be provided Yes * * Bold specifications are the golden parameters. * Bidders may note that In respect of non-golden Parameters
Requiredthe specifications 'Values' chosen by Buyer will generally be preferred over 'Bid requirement ( allowed Values) by the Buyer.
