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Departments Of Health And Family Welfare

Ahmedabad, Gujarat

  • Opening Date

    -

  • Closing Date

    09 Oct 2019

  • Tender Amount

    Refer document

  • EMD

    ₹ 25,000

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Summary

Tender Bid For Requirement Of Laboratory Consumables Items On Rate Contract As Mentioned In The Tender From Manufacturer/ Authorized Dealers/ Reputed Contractors Are Invited Online (internet). (part 1)

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M & J INSTITUTE OF OPHTHALMOLOGY - LAB TENDER YEAR 2019 - 2020 ANNEXURE - 1 Technical specification of Air sampler system  Mutable to fit with 90 mm & 100 mm Petri plate,  Aspiration volume of air is 30/60/100 liters/ min,  powder coated aluminum material,  With remote control & rechargeable battery operated with adjustable air flow rate. Other requirements:  Should provide ISO marked/CE marked/ FDA marked & GMP certificate  Should provide Product catalogue, manufactures authorizations letter and customers list.  Should provide Warranty for 2 years & CMC price next 5 years, which should include cost of labor spares, entire equipment. The CMC cost will be taken into consideration for price comparison.  Service engineer to be based in Gujarat preferably. ANNEXURE - 2 Technical specification of Autoclave  Should be vertical autoclave.  Pressure adjustable from 5 psi to 20 psi with an accuracy of +/- 1 psi, with automatic pressure control switch.  Outer and Inner chambers made up of stainless steel  Size of the inner chamber – 45 -50 x 70 -75 cm (Ǿ x D).  Should provide 2 carriers [Size: 35-40 X 30-35cm (Ǿ x D)] of stainless steel.  Should be provided with silicon gasket  Lid should be stainless steel and should be fitted with Pressure Gauge, Safety Valve, Manual exhaust valve, Vacuum breaker, Ports for calibration check.  All the hinges should be of stainless steel  Should be provided with stainless steel heated cover stand  Drain valve at bottom for draining the water  Heater should be 3.5KW  Micro processor controller based system to provide digital display of cycle processes like temperature, pressure  Should be provided with low water level alarm and cut off.  Automatic Pressure Control Switch - To cutoff the current from the heating elements, when the desired/ set pressure value level is attained inside the chamber and restarts the mechanism once the pressure inside the chamber falls from the desired level.  Should be fitted with chart and data recorder Other requirements:  Should provide ISO marked/CE marked/ FDA marked & GMP certificate  Should provide Product catalogue, manufactures authorizations letter and customers list.  Should provide Warranty for 2 years & CMC price next 5 years, which should include cost of labor spares, entire equipment. The CMC cost will be taken into consideration for price comparison.  Service engineer to be based in Gujarat preferably. ANNEXURE - 3 Technical specification of Fully Automated Rotary Microtome  Fully automatic motorized microtome with stepper motor driven specimen feed facility (hand- free facility) with manual option.  Section thickness selection from 0.5 to 100 um. Trimming step setting from 1 – 600 μm.  Vertical specimen stroke: 70 mm and horizontal object feed 28 mm via step motor  Two manual mode of sectioning by manual rotary action and by rocking action called ergo mode to minimized the risk of developing repetitive motion disorder(RMD)  Specimen retraction: in manual operation -5-10 um in 5 um increments can be turned off., in motorized operation : varying with sectioning speed can be trued of motorized coarse feed of 300 um and 900 um  Section speed -0.5-420 mm/s=/- 10%  Knife holder base with tungsten carbide disposable blade pack of 5, quantity 3 nos.  Specimen orientation of 8 degree with antilitter feature  Motor overload protection  Histo resin kit using hardener, liquid compound, Teflon mould tray, specimen block, lateral displacement with three – stop position.  They should provide the calibration certificate form NABL recognized testing laboratory May be preferred automatic hand free computer aided section cutting Other requirements:  Should provide ISO marked/CE marked/ FDA marked & GMP certificate  Should provide Product catalogue, manufactures authorizations letter and

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