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Tender For supply of group tender of medical equipment for histopathology, pathology, microbiology and blood bank dept. - grossing station automated , microtome- fully automated , lab incubator , hot air ove , ph meter , hot plate , semi automatic microtome , esr analyzer , embedding station with hot & cold table & paraffin dispenser , tissue floatation bath , lab refrigerator , electronic balance , slide filing cabinet , block filing cabinet , centrifuge , microscope binocular , microscope binocular with illumination & photography , hematology analyzer-3 part , semi automatic coagulometer , fully automated coagulation analyzer , elisareader with washer , vertical gel electrophoresis system , ultra deep freezer -80 deg c , cytospin , blood donor couch , blood collection monitor , dielectric tube sealer, handheld , refrigerated blood component transport box , (-40) degree deep freezer , vertical deep freezer - 20deg , ultra high speed centrifuge , plasma thawing bath , blood bank refrigerator , blood bag weighting balance- single pan , water bath , blood gas analyser , autoclave , bacteriological incubator , co2 incubator , anaerobic incubator , laminar air flow , bio safety cabinet class ii type b2 , ultrapure water purification system , fully automated colony counter , technical specification for compound microscope for microbiology
Tender For annual maintenance contract of pvms no- 270200, fully automated elisareader/ processor for pathology on ste single bid basis period of 01 year, inhs asvini
Tender For supply of srph326132-leptospira igm elisa :1.kit should be able to detect igm antibodies against l eptospira antigen in human serum. 2. should be a solid phase enzyme-linked immunosorbent assay (e lisa) based on the sandwich principle. 3. should be compatible with all common elisareader. 4. the assay component should include reactive and non- reactive controls. 5.test should have a sensiti vity of greater than and equal to 97% and specificity of greater than and equal to 99%. 6.adequat e documents detailing principle, components, bio safety, methodologies, limitations of assays, man ufacturing & expiry dates should be provided with each kit. 7. the kit to be procured should have approval of the statutory authority in its country of origin. 8. in case of imported kits it should h ave been registered and licensed in india by dcg (i). 9. in case of indigenous manufacturers they sha ll have license issued by the competent authority defined under drugs and cosmetics act, 1940 aft er appropriate evaluation by the centers approved by dcg (i). 10. the kit should have minimum shelf life of 18 months 1to 30 degree celsius. 11. kit for 96 tests. unit: test. ]