(SR PH CODE 326088) CRP-LATEX AGGLUTINATION ASSAY (REAGENT FOR SEMI AUTO ANALYSERS) Unit:TEST ]
3
(SR PH CODE 326093)DENGUE ANTIGEN/IGM/IGG DETECTION(RAPID) TESTUnit: TEST ]
4
SRPH346350-VACUTAINER NEEDLE WITH VISIBILITY OF BLOOD ENTRY 21G FOR MULTI-SAMPLE COLLECTION SHOULD HAVE THE FOLLOWING SPECIFICATIONS: 1). THE DESIGNING OF THE NEEDLES SHOULD BE SUCH THAT IT CAN ABLE TO MINIMIZE THE PRE- ANALYTICAL VARIABILITY THROUGHOUT THE SPECIMEN COLLECTION AND HANDLING PROCESS TO ENSURE RELIABLE RESULTS AND SHOULD BE SUITABLE FOR FASTER PROCEDURES. 2). THE NEEDLES SHOULD BE SUITABLE FOR CLOSED- SYSTEM BLOOD COLLECTION I.E DRAWING BLOOD DIRECTLY FROM THE VEIN INTO VACUUM COLLECTION TUBES TO PREVENT EXPOSURE OF ATMOSPHERE. 3). THE NEEDLES SHOULD BE SUITABLE FOR MULTI- SAMPLE COLLECTION.4). NEEDLES SHOULD BE STERILE, DOUBLE-ENDED WITH A SLEEVE COVERED SAFETY VALVE FOR USE WITH VACUTAINER TUBE HOLDER AND VACUUM BLOOD COLLECTION TUBES. 5). SIZE OF THE NEEDLE SHOULD BE 21G X 1 INCH (GAUGE: 21G, LENGTH: 1 INCH./25 MM).6) NEEDLE DESIGN SHOULD PROVIDE INSTANT CONFIRMATION OF NEEDLE PLACEMENT, THROUGH VISUAL FLASHBACK INDICATION.7). THERE SHOULD BE A CHAMBER OR SIMILAR ARRANGEMENT AT THE NEEDLE JUNCTION FOR EASY VISUAL CONFIRMATION OFBLOOD FLOW ENTRY.8). NEEDLE SHOULD HAVE LOW-ANGLE BEVEL DESIGN AND SHOULD BE COATED WITH SILICONE/ SIMILAR LOW FRICTION LUBRICANT COATING TO ENSURE GENTLE AND SMOOTH VEIN ENTRY (FOR SMOOTH PAINLESS PRICKING TO THE PATIENTS 9). THE FIRM SHOULD PROVIDE CERTIFICATE OF COMPLIANCE REPORT FOR EVERY BATCH AND MATERIAL USED FOR MAKING THE NEEDLE AND STERILIZATION OF THE NEEDLE SHOULD COMPLY WITH ISO STANDARDS.10). THE PRODUCT SHOULD BE BIS/ISO/CE/US FDA CERTIFIED AND SHOULD PRODUCE THE CERTIFICATE WHILE QUOTING IN THE TENDER.11). THE FIRM SHOULD SUPPLY SUITABLE NEEDLE HOLDERS ALONG WITH THE NEEDLE SUPPLY AND ALSO SHOULD SUBMIT ADEQUATE SAMPLING MATERIAL FOR CHECKING SUITABILITY & FOR VALIDATION, VERIFICATION OF PRODUCTUnit:NO ]
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