TENDER DOCUMENT. NIT No.: NRO/CON/738/672 Date: FOR VOLUME III BILL OF QUANTITY / PRICE BID ENGINEERING PROJECTS (INDIA) LIMITED

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1 TENDER DOCUMENT NIT : NRO/CON/738/672 Date: FOR Supply, Installation, Testing, Commissioning & Handingover of Medical equipments (Group-7E) for Government Medical College, Barmer (Rajasthan). VOLUME III BILL OF QUANTITY / PRICE BID ENGINEERING PROJECTS (INDIA) LIMITED (A GOVT. OF INDIA ENTERPRISE) Core-3, Scope Complex, 7,Lodhi Road, New Delhi TEL NO: , FAX NO

2 PRICE BID Supply, Installation, Testing, Commissioning & Handing- over of Medical equipments (Group-7E) for Government Medical College, Barmer (Rajasthan). SUMMARY OF COST SL. ITEM BIDDER'S PRICE ESTIMATED COST BELOW / AT PAR (IN Rs.) In figures ESTIMATED COST OF 1 MEDICAL EQUIPMENTS AS PER BOQ In words : Note:- i) Quoted rates shall be inclusive of all taxes & duties including GST. ii) quoted amount by the bidder shall be considered for price evaluation. BIDDER'S FINANCIAL OFFER : In Figures: SEAL In Words: SIGNATURE

3 BOQ for Supply, Installation, Testing, Commissioning & Handing - over of Medical (Group - 7E) for Government Medical College, Barmer (Rajasthan) 1 Automatic Gas Analyzer With Bicycle Ergometer Gas analysis -automatic for C02, 02 The System should be able to Record & measure VO2 oxygen consumption, VCO2 carbon dioxide production, VE Expired minute volume, RER respiratory exchange ratio, ECG, HRV, Body Temperature and Pressure Saturate BTPS, Standard Temperature and Pressure Dry STPD, (VE /VO2), (VE /VCO2) etc. and should generates a number of graphs like Metabolic Log Window, VE (BTPS) vs. VO2, VE (BTPS) vs.vco2, VCO2 vs. VO2, RER vs. time, VO2 vs. time, VCO2 v s. time. VE (BTPS) vs. time. High speed USB based recording unit along with Gas analysers. spirnmeter amplifier, flow- head and other transducers and accessories. Have oxygen sensor with minimum range of 5-100% oxygen and resolution of at least 0.02%, and the carbon dioxide sensor with minimum range 0-8% of carbon dioxide and resolution of at least 0. 1% and variable flow range of ml/min for best performance and results. To perform online and offline analysis up to 32 channels. Supplied with breathing accessories and Douglas bags. To plot real time flow & volume loops. ECG switch box (lead I, II, III, avl, avf, avr and VI to V6) for real time cardiac axis and vector analysis. IEC & ISO 9001 :2008 certified & making them safe for use with human subjects. An obligatory demonstration of the equipment and necessary training. To be supplied with Bicycle ergometer, branded computer & UPS. Automated ELISA Analyzer 2 It should be a Fully Automated ELISA System capable of dispensing sample, reagents, incubation, shaking, washing, reading in microwells. It should be operated by external PC. It should be able to perform 6 same or differ ent protocols in the same batch. It should be able to do qualitative, s emiquantitative and quantit a tive ELISAs. It should use minmum75 mm primary tubes It should use different plate geometries in Flat, U and V bottom It should have external barcode reader for samples Quantitative tests should support different calibration curve such as Point-to-Point,Linear Regression, Polynomial Regression, Cubic Spline, Logit-log, Lin-Log It should take max. 10 calibarators I standards per test in quantitative assay The Reader wavelength range should be nm It should have four filters 405nm, 450 nm, 492 nm and 630 nm It should read one strip in 20 seconds for a single wavelength The shaker should have stepper or continuous mode The washer should be 8 channel manifold The residual volume should not be more than 10 microliters It should have facility for 3 wash buffer bottles of 1L with level se nsors and 1rinse and 1wa s te bottle. It should perform maintenance procedures s uch as Wa s h (Auto W ash, Probe W ash), Prime, Strip cleaning the incubator should have RT or 37 Deg Temperature The system should hold 30 nos. 8 well ELISA strips without plate frames It should take maximum 58 samples I batch It should have a reagent cum sample tray and should hold sample, reagents and disposable tips. Maximum 30 positions for calibrators/ standards/ controls should be provided. Maximum 204 disposable carbonated tips should be possible to be loaded on the tr ay. Sample and reagent dispensing with fixed a nd carbonated tips. It should be user progra mmable. It s hould have 6/12 ml reage nt bottle locations QC reports a re ge nerated using U Cha rt I CV Evolution I O.D Evo lution I Cone Evolution &Westgard Rules Company onroll service engineer should be based at Rajasthan Shall be CE certified. f'irm should ensure rodent control for their instrument. Operating Environment Power Requirem ents AC 230V, 5 Power Consumption 200 VA Ambient Room Temperature C Storage Temperature C Page 1 of 3

4 Relative Humidityupto 90% relative humidity without condensation Dimensions mm L x mm B-x mm H Weight 75 Kgs 3 Automatic coagulation Analyzer It should have High Throughput continuous, random access fully automated analyzer with STAT Capability at any position used for hemostasis testing It should be Capable performing Clotting, Chromogenic & immunological tests like PT, APTI,TT, Fibrinog en, Protein C, Protein S, Free Protein S,Ahtithrombin, D-Dimer, VWF Ag,vWF Activity, Plasminogen, Anti plasmin, Homocysteine, Factor assays (clotting) & other Special Parameter, FXIII Ag. lntergrated tests for drvvt and SCT (Screen and Confirrn reagents). It should be Based on centrifugal technology can perform atleast 140 tests of PT and 100 tests of APTI in an hour. It should accommodate at least twenty reagents and samples which can be put in primary tubes/ sample cups at a time. It should have probes for sample and for reagent handling separately. It should have LCD touch screen, external printer, on board internal reader for the positive identification of samples and barcode reader for the reagents It should have Capability of at least 40 sample positions with the ability to use both primary tubes and sample cups simultaneously with or without barcode It should have Continuous loading of reagents, samples and consumables (cuvettes) and STAT samples without interrupting the workflow of the analyzer It should have automated dilution of samples, standards and controls with the ability to do automatic redilution in case of test results beyond the linearity of the assay (rerun) and reflex testing. It should have complete internal QC program with different levels of controls and charts (Levey Jennings ). It should have Automatic liquid level detection for samples and reagents Company should have all reagents and calibrators/ quality controls for smooth running. It should have Storage of patient records It s hould be USFDA approv ed and certificate must be enclose with the bid. Firm should ensure rodent control for their instrument. Firm shall provide list of consumables and reagents used in the equipments in the technical bid Firm shall provide split Air conditioner of 1.5 tonn 5 star rated 4 Firm shall provide the user list from NABL accredited labs 5 Part Hematology Analyzer The instrument should be fully automated fluorescence flow cytometry based 5-part differential hematology analyzer offering automatic start-up, shutdown and sample-analysis. The instrument should have random access discrete analysis modes forcbc, CBC+DIFFERENTIAL+ IG. 2 2 The instrument should have 24 PARAMETERS reported: WBC, RBC, HGB, HCT, MCV, MCH, MCHC,RDW-SD, RDW- CV, PLT, NEUT %, LYMPH%, MONO%, EOS %, BASO %, NEUT #, LYMPH#, MONO#, EOS #, BASO #,POW, MPV, PCT, P-LCR, IG#, IG% TWO HISTOGRAMS- RBC, PLT and ONE SCATTERGRAM The instrument should have throughput of atleast 60 samples per hour in both the discrete analysis modes and auto loaded mode. The Sample aspiration volume for the complete differential blood count should not be more than 70 ul. The instrument should have the following analysis modes, Manual - open & Capillary mode. The instrument should have Hydrodynamic focusing / impedance method for RBC/PLT channel. The instrument should have Cyanide free Sls-hb / colorimetric method for the hemoglobin measurement The instrument should be equipped with Fluorescence based semiconductor laser fluorescence flow cytometry for differential channel. instrument should be able to enumerate immature granulocytes. The instrument should have comprehensive information processing system with User-friendly Windows XP/ 7 based software. Page 2 of 3

5 5 The instrument should have minimum maintenance cost. It should have high linearity of over 4 lacs for WBC's,over 40 lacs for platelets It should be supported by Company's on-roll Service Engineers based in various cities in Rajasthan. The system should be USFDA approved Firm should ensure rodent control for their instrument. Firm shall provide list of consumables and reagents used in 1ments in the technical bid Firm shall calibrate the equipment annually free of cost. Firm shall provide the user list from NABL accredited labs. The firm shall attend the breakdown within three days. The firm should provide a complete set of reagents at the time of installation HbA1C Analyzer 1. Fully automated bench top integrated system for measurement of HbAlc. 2. The system should be based on high performance liquid chromatography (HPLC) technology 3. The system should have faster throughput of<3.5 minutes per sample 4. Complete ready to use kit with Buffers, Column,Calibrator and sample vials. 5. The system should contain low pulsation dual syringe pump with programmable buffer delivery 6. The system should be able to run sample from both primary tube and outside dilution mode 7. The system should be CE certified 8. The system should be NGSP (National Glycohemoglobin Standardization Program) certified. 9. The system should have complete elimination of labile glycohemoglobin(labile Ale) ensuring accurate HbA1c results 10. The system should be able to give HbF& HbA2 flag in A1c mode 11. The system s hould accept multiple samples tubes size including primary tubes, microcapillary tubes, 1.5 ml samp le tubes etc 12. The system should have large color display for ease of operation 13. The system should have software to view real time chromatogram s of samples analysis 14. The system should have in-built barcode reader for positive samples identification 15. The system should have bidirectional LIS facility 16.The system should have on board QC monitoring with Levey-Jennings and statistical calculations 17. The system should be free from interference from common Hb variants including heterozygous HbS, HbC, HbD, HbE 18. The system should have RFID for reagent tracking and identification 19. The system should have unlimited storage of calibration, QC data and chromatograms. 20. The company should be able to provide normal and abnormal control for HbAlc 21. The system should have external USB ports 22. The system should have in built thermal printer for printing results and should have facility to connect external Laser printer. 23.The system should have facility to customize sample result report bas,ed on customer requirement 24. It should be supported by Company's on-roll Service Engineers based in various cities of Rajasthan. (Demonstration is must.) Grand ( Rs..... only) Note:- i) Quoted rates shall be inclusive of all taxes & duties including GST. ii) quoted amount by the bidder shall be considered for price evaluation. Page 3 of 3