Surat Municipal Corporation-SMC has published Tender For Procurement Of Kits,Blood Bags, Vacutainer, Etc., Items. Submission Date for this Tender is 13-07-2020. Blood Bank Analyzers Tenders in Gujarat. Bidders can get complete Tender details and download the document.
| S.NO | TenderItemID | Store Code | Item Serial | ItemCode | Item Name | Specification | DelDays | Quantity | Unit Description | EMD RS. |
| 1 . | 1 | M1 | 1 | 23/001/0020/00/0/0/0 | MULTISTIX--BOTTLE OF 100 STRIP | - | 40 | 25 | BOTTLE Of 100 STRIP | 200 |
| 2 . | 2 | M1 | 2 | 23/001/0021/00/0/0/0 | KETODIASTIX STRIP FOR DETECT OF SUGAR,ACETONE IN URINE-BOTLE 50STRIP | - | 40 | 90 | BOTTLE Of 50 STRIP | 100 |
| 3 . | 3 | M1 | 3 | 23/001/0022/00/0/0/0 | HAEM TEST (OCULT BLOOD TEST) | - | 40 | 3500 | TEST | 200 |
| 4 . | 4 | M1 | 4 | 23/001/0023/00/0/0/0 | URISTIX STRIPS--BOTTLE OF 100 STRIP | - | 40 | 650 | BOTTLE Of 100 STRIP | 500 |
| 5 . | 5 | M1 | 5 | 23/001/0135/00/0/0/0 | CALCIUM KIT ARSENAZO-III METHOD END POINT | (THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS) NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 100 ML | 40 | 11000 | MILILITER | 200 |
| 6 . | 6 | M1 | 6 | 23/001/0136/00/0/0/0 | CHOLINESTRASE BUTIRYL THIOCHOLINE/PROPIONYL THIOCHOLINE SUBSTRATE | SUBSTRATE, KINETIC (THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS) NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 25 ML | 40 | 200 | MILILITER | 100 |
| 7 . | 7 | M1 | 7 | 23/001/0139/00/0/0/0 | HbsAg ELISA KIT BASE ON 3RD GEN.(MONOCLONAL ANTIBODIES) | - | 40 | 25000 | TEST | 2100 |
| 8 . | 8 | M1 | 8 | 23/001/0140/00/0/0/0 | HCV ELISA KIT | TO REFER TECHNICAL BID FOR SPECIFICATION "Should be FDA/CE/WHO certified company. "Principle -: Qualitative enzyme immunoassay kit for the detection of antibody against HCV (anti-HCV) in human serum or plasma."Use of combination of HCV antigens for Core, NS3,NS4, & NS5.(Additional E1,E2 Will be Preferred)"Sensitivity -: 100 %"Specificity -: More than 97 %"Shelf life -: Minimum nine months at the time of delivery."Pack size -: 96 Tests."Easy to use on automated and semi-automatic processor. "Company will have to provide additional wash buffer and control if required."Sensitivity & Specificity should be determined by WHO/Government authority. "company should provide the trace record for temprature maintainance during storage and transport. | 40 | 20000 | TEST | 2600 |
| 9 . | 9 | M1 | 9 | 23/001/0141/00/0/0/0 | HCV RAPID KIT STRIP TEST (IC) | - | 40 | 4400 | TEST | 1000 |
| 10 . | 10 | M1 | 10 | 23/001/0156/00/0/0/0 | TOTAL PROTEIN KIT BIURET METHOD END POINT | NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 50000 | MILILITER | 300 |
| 11 . | 11 | M1 | 11 | 23/001/0157/00/0/0/0 | VDRL-RPR CARD TEST WITH CONTROLS(CHARCOAL ANTIGEN&ACCS) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 100 TEST | 40 | 38000 | TEST | 700 |
| 12 . | 12 | M1 | 12 | 23/001/0229/00/0/0/0 | DOUBLE BLOOD BAG 350ML | TO REFER TECHNICAL BID FOR SPECIFICATION. QUALITY CERTIFICATES:"CE MARK, ISO 9001-2000, DIRECTIVE 93/42/EEC, ISO 13485:1996 QUALITY SYSTEM CERTIFICATION."CONFORMITY TO ALL STANDARDS OF ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS, TEST REPORT SHOULD BE SUBMITTED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. THE NEEDLE:"NEEDLE SHOULD GENERATE LESS THAN 16 GM FORCE OF RESISTANCE THUS ENSURING VIRTUALLY PAINLESS VENEPUNCTURE EVERY TIME."NEEDLE SHOULD HAVE HARD OUTER COVERING, WHICH WILL PREVENT THE NEEDLE GETTING BENT IN ORDER TO MAINTAIN SHARPNESS AND A SMOOTH VENEPUNCTURE. THE FEATURE SHOULD HAVE A MARKET STANDING OF AT LEAST 15 YEARS "16 GAUGE ULTRA THIN WALLED AND STRAIGHT FOR ASSURING SMOOTH AND ATREMATIC VENIPUNCHERE FOR MAXIMUM COMFORT AND MINIMUM PAIN. MARKINGS IN THE TUBING: "SEGMENT NUMBERING THROUGH THERMIC TECHNOLOGY AND NUMBERS SHOULD BE VERY CLEAR, LEGIBLE AND READABLE WITH OUT ANY STRAINS TO EYES.THE MATERIAL:"THE BLOOD BAG MATERIAL SHOULD BE K80 TO ENSURE THE QUALITY OF STORED BLOOD AND STRENGTH DURING CENTRIFUGATION.CAPACITY:"PRIMARY BLOOD BAG HAVING CPDA SOLUTION - 450 ML ."TRANSFER BAG CAPACITY UP TO 400 ML.ANTICOAGULANT AND PRESERVATIVE SOLUTION:"CPDA (63 ML I.E. 14 ML/ 100 ML OF BLOOD)."CLEAR & COLORLESS."NO DISCOLORATION ON STORAGE AT ROOM TEMPERATURE.EXTERNAL STERILITY OF BLOOD BAGS:"THE BLOOD BAGS SHOULD BE FIRST STERILISED AND THEN PACKED IN THE POLYPROPYLENE COVER TO PREVENT FUNGAL SPORES TO SETTLE ON THE SURFACE OF BAG AND DEVELOP INTO FUNGUS."CERTIFICATE OF VALIDATION OF STERILISER. THE MANUFACTURER SHOULD GIVE CAPACITY FOR EACH KIND OF BAG, THE MANUFACTURER SHOULD GIVE RECORDS OF HEAT PENETRATION STUDIES TO ESTABLISH STERILISATION CONDITIONS TO MEET EN 554 WELDING TECHNOLOGY:"BLOOD BAGS SHOULD BE WELDED WITH HIGH FREQUENCY SEALING TECHNOLOGY, WHICH ENSURES THAT BAGS DO NOT BREAK EVEN WHEN CENTRIFUGED AT HIGH SPEEDS.TAMPER EVIDENT TRANSFUSION PORT:"IT SHOULD HAVE A PEEL OFF TAMPER EVIDENT TRANSFUSION PORT WITH SINGLE HAND OPERATION AND PEEL OFF PORTION SHOULD BE INTEGRATED ALONG WITH THE BAG .BREAK OFF VALVE:"THE BAG SHOULD HAVE BREAK OFF VALVE WITH CLEAR CUT BREAK-AWAY LINE AND OPTIMAL SHAPE DESIGNED TO ENABLE FAST AND SHOULD BE EASIER TO BREAK.LABEL:"LABELS ON BLOOD BAGS SHOULD BE PASTED WITH HOT MARK TECHNOLOGY AND SHOULD HAVE BARCODE. "NON-PEAL OFF"HEAT SEALED LABELS OR PRESSURE SENSITIVE LABELS."REMAIN ATTACHED BETWEEN ROOM TEMPERATURE TO -80?C WITH A TRANSPARENT ADHESIVE, HIGHLY RESISTANT AGAINST WEAR AND TEAR."DATE OF MANUFACTURING, DATE OF EXPIRY AND LOT NUMBER MUST BE MENTIONED ON EACH BAG"THE EXPIRY DATE SHOULD BE AT LEAST 2 YEARS FROM THE DATE OF MANUFACTURE OF BLOOD BAGS OR 20 MONTHS FROM THE DATE OF SUPPLY.PACKING:"THE SHIPPER CARTON SHOULD BE A 7 PLY CORRUGATED CARTON MADE OF 200-GSM CRAFT PAPER AT TOP LAYER AND OTHER LAYERS MADE OF VIRGIN CRAFT PAPER. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE | 40 | 2000 | NUMBER | 2400 |
| 13 . | 13 | M1 | 13 | 23/001/0249/00/0/0/0 | DOUBLE BLOOD BAG 450ML WITH SAGM | TO REFER TECHNICAL BID FOR SPECIFICATION QUALITY CERTIFICATES:"CE MARK, ISO 9001-2000, DIRECTIVE 93/42/EEC, ISO 13485:1996 QUALITY SYSTEM CERTIFICATION."CONFORMITY TO ALL STANDARDS OF ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS, TEST REPORT SHOULD BE SUBMITTED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. THE NEEDLE:"NEEDLE SHOULD GENERATE LESS THAN 16 GM FORCE OF RESISTANCE THUS ENSURING VIRTUALLY PAINLESS VENEPUNCTURE EVERY TIME."NEEDLE SHOULD HAVE HARD OUTER COVERING, WHICH WILL PREVENT THE NEEDLE GETTING BENT IN ORDER TO MAINTAIN SHARPNESS AND A SMOOTH VENEPUNCTURE. THE FEATURE SHOULD HAVE A MARKET STANDING OF AT LEAST 15 YEARS "16 GAUGE ULTRA THIN WALLED AND STRAIGHT FOR ASSURING SMOOTH AND ATREMATIC VENIPUNCHERE FOR MAXIMUM COMFORT AND MINIMUM PAIN. THE MATERIAL:"THE BLOOD BAG MATERIAL SHOULD BE K80 TO ENSURE THE QUALITY OF STORED BLOOD AND STRENGTH DURING CENTRIFUGATION.CAPACITY:"PRIMARY BLOOD BAG HAVING CPDA SOLUTION - 450 ML ."SECONDARY BAG WITH SAGM & ADDITIONAL SOLUTION 400 ML CAPACITY ANTICOAGULANT AND PRESERVATIVE SOLUTION:"CPD (63 ML I.E. 14 ML/ 100 ML OF BLOOD)."SAGM & ADDITIONAL SOLUTION 100 ML."CLEAR & COLORLESS."NO DISCOLORATION ON STORAGE AT ROOM TEMPERATURE. EXTERNAL STERILITY OF BLOOD BAGS:"THE BLOOD BAGS SHOULD BE FIRST STERILISED AND THEN PACKED IN THE POLYPROPYLENE COVER TO PREVENT FUNGAL SPORES TO SETTLE ON THE SURFACE OF BAG AND DEVELOP INTO FUNGUS."CERTIFICATE OF VALIDATION OF STERILISER. THE MANUFACTURER SHOULD GIVE CAPACITY FOR EACH KIND OF BAG, THE MANUFACTURER SHOULD GIVE RECORDS OF HEAT PENETRATION STUDIES TO ESTABLISH STERILISATION CONDITIONS TO MEET EN 554 WELDING TECHNOLOGY:"BLOOD BAGS SHOULD BE WELDED WITH HIGH FREQUENCY SEALING TECHNOLOGY, WHICH ENSURES THAT BAGS DO NOT BREAK EVEN WHEN CENTRIFUGED AT HIGH SPEEDS.TAMPER EVIDENT TRANSFUSION PORT:"IT SHOULD HAVE A PEEL OFF TAMPER EVIDENT TRANSFUSION PORT WITH SINGLE HAND OPERATION AND PEEL OFF PORTION SHOULD BE INTEGRATED ALONG WITH THE BAG .LABEL:"LABELS ON BLOOD BAGS SHOULD BE PASTED WITH HOT MARK TECHNOLOGY AND SHOULD HAVE BARCODE. "NON-PEAL OFF"HEAT SEALED LABELS OR PRESSURE SENSITIVE LABELS."REMAIN ATTACHED BETWEEN ROOM TEMPERATURE TO -80?C WITH A TRANSPARENT ADHESIVE, HIGHLY RESISTANT AGAINST WEAR AND TEAR."DATE OF MANUFACTURING, DATE OF EXPIRY AND LOT NUMBER MUST BE MENTIONED ON EACH BAG"THE EXPIRY DATE SHOULD BE AT LEAST 2 YEARS FROM THE DATE OF MANUFACTURE OF BLOOD BAGS OR 20 MONTHS FROM THE DATE OF SUPPLY. MARKINGS IN THE TUBING: "SEGMENT NUMBERING THROUGH THERMIC TECHNOLOGY AND NUMBERS SHOULD BE VERY CLEAR, LEGIBLE AND READABLE WITH OUT ANY STRAINS TO EYES.BREAK OFF VALVE:"THE BAG SHOULD HAVE BREAK OFF VALVE WITH CLEAR CUT BREAK-AWAY LINE AND OPTIMAL SHAPE DESIGNED TO ENABLE FAST AND SHOULD BE EASIER TO BREAK.PACKING:"THE SHIPPER CARTON SHOULD BE A 7 PLY CORRUGATED CARTON MADE OF 200-GSM CRAFT PAPER AT TOP LAYER AND OTHER LAYERS MADE OF VIRGIN CRAFT PAPER. THE ALUMINUM FOIL PACK | 40 | 5000 | NUMBER | 7200 |
| 14 . | 14 | M1 | 14 | 23/001/0252/00/0/0/0 | TRANSFER BAG 300ML CAPA.,FDA,APROVED,QUALITY CERTI.(CE,ISO-9001-2000) | - | 40 | 1000 | NUMBER | 800 |
| 15 . | 15 | M1 | 15 | 23/001/0268/00/0/0/0 | TRIPLE BLOOD BAG WITH SAGM 450ML | FOR SPECIFICATION REFER TECHNICAL BID QUALITY CERTIFICATES:"CE MARK, "ISO 9001-2000, "DIRECTIVE 93/42/EEC, "ISO 13485:1996 QUALITY SYSTEM CERTIFICATION. CONFORMITY TO ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS. TEST REPORT SHOULD BE SUBMITTED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. NEEDLE:"NEEDLE IS GENERATE LESS THAN 17 GM FORCE OF RESISTANCE THUS ENSURING VIRTUALLY PAINLESS VENEPUNCTURE EVERY TIME."OUR NEEDLE HAVE HARD OUTER COVERING WHICH WILL PREVENT THE NEEDLE GETTING BENT IN ORDER TO MAINTAIN SHARPNESS AND A SMOOTH VENEPUNCTURE. THIS FUTURE IS HAVING MARKET STANDING OF MORE THAN 2 YEARS "16 GAUGE ULTRA THIN WALLED AND STRAIGHT FOR ASSURING SMOOTH AND ATREMATIC VENIPUNCHERE FOR MAXIMUM COMFORT AND MINIMUM PAIN. MARKINGS IN THE TUBING: "SEGMENT NUMBERING THROUGH THERMIC TECHNOLOGY AND NUMBERS SHOULD BE VERY CLEAR, LEGIBLE AND READABLE WITH OUT ANY STRAINS TO EYESSTERILITY BLOOD BAGS - (EXTERNAL)"OUR BLOOD BAGS ARE TO BE 1ST STERILISED AND THEN PACKED IN THE POLYPROPYLENE COVER TO PREVENT FUNGAL SPORES TO SETTLE ON THE SURFACE OF BAG AND DEVELOP INTO FUNGUS."CERTIFICATE OF VALIDATION OF STERILISER. THE MANUFACTURER SHOULD GIVE CAPACITY FOR EACH KIND OF BAG, THE MANUFACTURER SHOULD GIVE RECORDS OF HEAT PENETRATION STUDIES TO ESTABLISH STERILISATION CONDITIONS TO MEET EN 554 CAPACITY:"PRIMARY BLOOD BAG HAVING CPD SOLUTION-450 ML BAG."TRANSFER BAG CAPACITY UP TO 400 ML WITH 100 ML SAGM."FOR PLATELET TRANSFER BAG PLASTICIZED TRANSFER BAG WITH SUFFICIENT GAS PERMEABILITY.ANTICOAGULANT AND PRESERVATIVE SOLUTION:"CPD (63 ML I.E. 14 ML/ 100 ML OF BLOOD)."SAGM & ADDITIONAL SOLUTION 100 ML."CLEAR & COLORLESS."NO DISCOLORATION ON STORAGE AT ROOM TEMPERATURE.WELDING TECHNOLOGY:"BLOOD BAGS SHOULD BE WELDED WITH HIGH FREQUENCY SEALING TECHNOLOGY WHICH ENSURES THAT BAGS DO NOT BREAK EVEN WHEN CENTRIFUGED AT HIGH SPEEDS.TAMPER EVIDENT TRANSFUSION PORT:"IT SHOULD HAVE A PEEL OFF TAMPER EVIDENT TRANSFUSION PORT WITH SINGLE HAND OPERATION AND PEEL OFF PORTION SHOULD BE INTEGRATED ALONG WITH THE BAG BREAK OFF VALVE:"THE BAG SHOULD HAVE BREAK OFF VALVE WITH CLEAR CUT BREAK-AWAY LINE AND OPTIMAL SHAPE DESIGNED TO ENABLE FAST TRANSFER BOTH IN THE MOTHER BAG AND SAGM BAG FOR SMOOTH TRANSFER OF COMPONENTS AND SHOULD BE EASIER TO BREAK.LABEL:"LABELS ON BLOOD BAGS SHOULD BE PASTED WITH HOT MARK TECHNOLOGY AND SHOULD HAVE BARCODE. "NON-PEAL OFF"HEAT SEALED LABELS OR PRESSURE SENSITIVE LABELS."REMAIN ATTACHED BETWEEN ROOM TEMPERATURE TO -80?C WITH A TRANSPARENT ADHESIVE, HIGHLY RESISTANT AGAINST WEAR AND TEAR."DATE OF MANUFACTURING, DATE OF EXPIRY AND LOT NUMBER MUST BE MENTIONED ON EACH BAG"THE EXPIRY DATE SHOULD BE AT LEAST 2 YEARS FROM THE DATE OF MANUFACTURE OF BLOOD BAGS OR 20 MONTHS FROM THE DATE OF SUPPLY. ALUMINIUM FOIL: IT SHOULD HAVE MORE THAN 2 LAYERS TO ENSURE THE STERILITY OF THE BAGS IS MAINTAINED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD B | 40 | 2500 | NUMBER | 5900 |
| 16 . | 16 | M1 | 16 | 23/001/0269/00/0/0/0 | DOUBLE BLOOD BAG 450ML | FOR SPECIFICATION REFER TECHNICAL BID "CE MARK, ISO 9001-2000, DIRECTIVE 93/42/EEC, ISO 13485:1996 QUALITY SYSTEM CERTIFICATION."CONFORMITY TO ALL STANDARDS OF ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS, TEST REPORT SHOULD BE SUBMITTED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. THE NEEDLE:"NEEDLE SHOULD GENERATE LESS THAN 16 GM FORCE OF RESISTANCE THUS ENSURING VIRTUALLY PAINLESS VENEPUNCTURE EVERY TIME."NEEDLE SHOULD HAVE HARD OUTER COVERING, WHICH WILL PREVENT THE NEEDLE GETTING BENT IN ORDER TO MAINTAIN SHARPNESS AND A SMOOTH VENEPUNCTURE. THE FEATURE SHOULD HAVE A MARKET STANDING OF AT LEAST 15 YEARS "16 GAUGE ULTRA THIN WALLED AND STRAIGHT FOR ASSURING SMOOTH AND ATREMATIC VENIPUNCHERE FOR MAXIMUM COMFORT AND MINIMUM PAIN. MARKINGS IN THE TUBING: "SEGMENT NUMBERING THROUGH THERMIC TECHNOLOGY AND NUMBERS SHOULD BE VERY CLEAR, LEGIBLE AND READABLE WITH OUT ANY STRAINS TO EYES.THE MATERIAL:"THE BLOOD BAG MATERIAL SHOULD BE K80 TO ENSURE THE QUALITY OF STORED BLOOD AND STRENGTH DURING CENTRIFUGATION.CAPACITY:"PRIMARY BLOOD BAG HAVING CPDA SOLUTION - 450 ML ."TRANSFER BAG CAPACITY UP TO 400 ML.ANTICOAGULANT AND PRESERVATIVE SOLUTION:"CPDA (63 ML I.E. 14 ML/ 100 ML OF BLOOD)."CLEAR & COLORLESS."NO DISCOLORATION ON STORAGE AT ROOM TEMPERATURE.EXTERNAL STERILITY OF BLOOD BAGS:"THE BLOOD BAGS SHOULD BE FIRST STERILISED AND THEN PACKED IN THE POLYPROPYLENE COVER TO PREVENT FUNGAL SPORES TO SETTLE ON THE SURFACE OF BAG AND DEVELOP INTO FUNGUS."CERTIFICATE OF VALIDATION OF STERILISER. THE MANUFACTURER SHOULD GIVE CAPACITY FOR EACH KIND OF BAG, THE MANUFACTURER SHOULD GIVE RECORDS OF HEAT PENETRATION STUDIES TO ESTABLISH STERILISATION CONDITIONS TO MEET EN 554 WELDING TECHNOLOGY:"BLOOD BAGS SHOULD BE WELDED WITH HIGH FREQUENCY SEALING TECHNOLOGY, WHICH ENSURES THAT BAGS DO NOT BREAK EVEN WHEN CENTRIFUGED AT HIGH SPEEDS.TAMPER EVIDENT TRANSFUSION PORT:"IT SHOULD HAVE A PEEL OFF TAMPER EVIDENT TRANSFUSION PORT WITH SINGLE HAND OPERATION AND PEEL OFF PORTION SHOULD BE INTEGRATED ALONG WITH THE BAG .BREAK OFF VALVE:"THE BAG SHOULD HAVE BREAK OFF VALVE WITH CLEAR CUT BREAK-AWAY LINE AND OPTIMAL SHAPE DESIGNED TO ENABLE FAST AND SHOULD BE EASIER TO BREAK.LABEL:"LABELS ON BLOOD BAGS SHOULD BE PASTED WITH HOT MARK TECHNOLOGY AND SHOULD HAVE BARCODE. "NON-PEAL OFF"HEAT SEALED LABELS OR PRESSURE SENSITIVE LABELS."REMAIN ATTACHED BETWEEN ROOM TEMPERATURE TO -80?C WITH A TRANSPARENT ADHESIVE, HIGHLY RESISTANT AGAINST WEAR AND TEAR."DATE OF MANUFACTURING, DATE OF EXPIRY AND LOT NUMBER MUST BE MENTIONED ON EACH BAG"THE EXPIRY DATE SHOULD BE AT LEAST 2 YEARS FROM THE DATE OF MANUFACTURE OF BLOOD BAGS OR 20 MONTHS FROM THE DATE OF SUPPLY.PACKING:"THE SHIPPER CARTON SHOULD BE A 7 PLY CORRUGATED CARTON MADE OF 200-GSM CRAFT PAPER AT TOP LAYER AND OTHER LAYERS MADE OF VIRGIN CRAFT PAPER. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. A | 40 | 2000 | NUMBER | 2400 |
| 17 . | 17 | M1 | 17 | 23/001/0270/00/0/0/0 | CPDA SINGLE BLOOD BAG 350ML | FOR SPECIFICATION REFER TECHNICAL BID "THE BLOOD BAGS MEETS THE FOLLOWING BIOLOGICAL REQUIREMENTS OF THE STORED BLOOD.NO.ACCEPTABLE VALUES(AT THE 28TH DAY)1.ATP (% OF INITIAL LEVEL)79.37 8.822.2,3 DPG (% OF INITIAL LEVEL)12.56 1.603.DEHP LEACHING(MG/100 ML WHOLE BLOOD)6.93 0.494.% HEAMOLYSIS0.421 0.315.PLASMA K MM/LITRE20.22 2.756.PH 6.942 0.035"BIO-COMPATIBILITY OF THE MATERIAL OF THE PLASTIC CONTAINER MUST BE CERTIFIED BY THE MANUFACTURER AND SUPPORTED BY TEST REPORTS OF THE FOLLOWING.1.CELL CULTURE CYTOTOXICITY2.HAEMOLYSIS3.SYSTEMIC INJECTION (ACUTE TOXICITY)4.SENSITISATION5.INTRACUTANEOUS INJECTION (IRRITATION)6.PYREGEN TEST 7.STERILITY "STABILITY STUDIES DATA TO PROVE 3 YEARS\ SHELF LIFE SHOULD BE PRODUCED"CE MARK AND ISO 9002 QUALITY SYSTEM CERTIFICATION"CONFORMITY TO ALL STANDARDS OF ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS, TEST REPORT SHOULD BE SUBMITTED. CONFORMITY TO ALL STANDARDS OF ISO 3826 INTERNATIONAL PRODUCT STANDARD FOR BLOOD BAGS, TEST REPORT SHOULD BE SUBMITTED. THE ALUMINUM FOIL PACK AND BLOOD BAG SHOULD BE MARKED WITH ISO 3826 FOR THE CONFIRMATION OF THE SAME. "IN HOUSE R & D CENTER RECOGINISED BY THE GOVERNMENT OF INDIA"MARKET STANDING OF 5 YEARS"CAPACITY : SINGLE BLOOD BAG-350 ML"AIR CONTENT: CONTAINER SHOULD NOT EXCEED 10ML "EXTERNAL STERILITY OF THE BLOOD BAGS MUST BE ASSURED"THE FIRM MUST SUBMIT PUBLISHED MATERIALS IN THE SCIENTIFIC JOURNALS IN FAVOURS OF THE QUALITY OF BLOOD BAGS"NEEDLE USED SHOULD ENABLE PAINLESS VENEPUNCTURE. THE NEEDLE PENETRATION FORCE SHOULD BE LESS THE 20GM FORCE."16 GAUGE ULTRA THIN WALLED AND STRAIGHT FOR ASSURING SMOOTH AND ATREMATIC VENIPUNCHERE FOR MAXIMUM COMFORT AND MINIMUM PAIN. "SHARP REGULAR MARGINS AND BEVELED TIP."RUST PROOF."TIGHTLY FIXED WITH HUB COVERED WITH STERILE GUARD."HERMETICALLY SEALED TO ENHANCES SAFETY."THE MANUFACTURER SHOULD PRODUCE PROOF THAT THE BAGS ARE BEING TESTED AS PER ISO 3826 STANDARDS"THE APPEARANCE OF THE SOLUTION SHOULD BE CLEAR AND COLORLESS"THE ASSAY OF THE ANTICOAGULANT SHOULD PROVE THAT ALL THE CONSTITUENTS ARE WITHIN LIMITS PRESCRIBED BY ISO 3826"CPDA-1 (49 ML I.E. 14 ML/ 100 ML OF BLOOD)."CLEAR & COLORLESS."NO DISCOLORATION ON STORAGE AT ROOM TEMPERATURE."TAMPER EVIDENT TRANSFUSION PORT"MEMORY LESS TUBINGMARKINGS IN THE TUBING: "SEGMENT NUMBERING THROUGH THERMIC TECHNOLOGY AND NUMBERS SHOULD BE VERY CLEAR, LEGIBLE AND READABLE WITH OUT ANY STRAINS TO EYES"LABEL: LABELS ON BLOOD BAGS SHOULD BE PASTED WITH HOT MARK TECHNOLOGY AND SHOULD HAVE BARCODE. "ALUMINIUM FOIL: IT SHOULD HAVE MORE THAN 2 LAYERS TO ENSURE THE STERILITY OF THE BAGS IS MAINTAINED.THE SHIPPER CARTON SHOULD BE A 7 PLY CORRUGATED CARTON MADE OF 200 GSM CRAFT PAPER ATOP LAYER AND OTHER LAYERS MADE OF VIRGIN CRAFT PAPER TO PREVENT NEEDLE DAMAGE | 40 | 100 | NUMBER | 100 |
| 18 . | 18 | M1 | 18 | 23/001/0281/00/0/0/0 | BLOOD BAG WITH LEUKOCYTE-DEPLETION FILTER | ISO-CE MARK,FDA APPROVED 1. SPECIAL BLOOD FILTER 2. TO REDUCE NUM OF WBC<5X106 | 40 | 100 | NUMBER | 1000 |
| 19 . | 19 | M1 | 19 | 23/001/0406/00/0/0/0 | SYPHILIS Ab RAPID TEST KIT ( DIP STRIP ) | TO REFER TECHNICAL BID FOR SPECIFICATION "Should be FDA/CE/WHO certified company."Principle -:Lateral flow chromatographic immunoassay Qualitative detection of Treponema Pallidum Antibodies ( IgM,IgA & IgG ) in human serum or plasma."Sensitivity -: 100 %"Specificity -: More than 99.7 %"Should have 1 control Band & 1 control Band for validation."Self life -: More than one year."Pack Size -: 50 to 100 Test"Sensitivity & Specificity should be determined by WHO/Government authority."company should provide the trace record for temprature maintainance during storage and transport. | 40 | 5500 | TEST | 400 |
| 20 . | 20 | M1 | 20 | 23/001/0407/00/0/0/0 | RAPID MALARIA KIT | FOR SPECIFICATION REFER TECHNICAL BID ISO / CE/ WHO /GMP CERTIFIED,INDIVIDUALLY POUCHES SINGLE TEST FOR DETECTION OF P F HRP(HISTIDINE RICH PROTEIN) & PLASMODIUM SPECIES (P FALCIPARUM/VIVAX/P MALARIE / P OVE/ PLDH ) IN HUMAN BLOOD,ANALYTICAL SENSITIVITY OF 50 PARASITES / UL BLOOD,SEE THROUGH DEVICE,LONGER SHELF LIFE (APPROXIMATELY ONE & HALF YEAR),RESULT SHOULD TAKE MINIMUM TIME ,SENSITIVITY SHOULD BE 100 %,SPECIFICITY SHOULD BE 100%,SENSITIVITY SHOULD BE 100 % & SPECIFICITY SHOULD BE 99 % WHICH SHOULD BE EVALUATED BY WHO/ GOVERNMENT BODY,PACK SIZE SHOULD BE 25/50 TEST, | 40 | 168000 | TEST | 28900 |
| 21 . | 21 | M1 | 21 | 23/001/0412/00/0/0/0 | LEPTOSPIRA RAPID KIT (FOR IgM DETECTION) | - | 40 | 50 | TEST | 100 |
| 22 . | 22 | M1 | 22 | 23/001/0610/00/0/0/0 | TOP & BOTTOM QUADRUPLE BLOOD BAG WITH INTEGRATED FILTER FOR COMPONENT | FOR SPECIFICATION REFER TECHNICAL BID "For separation of Leukocytes-depleted RBC, Plasma & Platelet."Minimal volume loss leads to better Red Blood Cell recovery."Simple process control, easy to implement into routine procedures."Transparent housing helps in visual monitoring during filtration. "Bag with inline filters to prepare leukodepleted blood. "It should have Needle Injury protector, Predonation bag and Leur adaptor to ensure more safety."Top and bottom bag should contain hot marking numbers in tubes of all bags including red cell, plasma and platelet."Mother bag should be with 0.45 mm thickness to prevent breakage during centrifugation and the inner diameter of the transfer tube from mother bag to SAGM bag is with 3.8 ID to provide easy flow of the component."Integrated filters should be made of biocompatible Polyurethane material to ensure the quality of component during filtration."Integrated filters should be with very soft housing to avoid breakage during centrifugation."Integrated filter should have a clamp attached to the filters to make priming procedure more comfortable."Recovery of red cell after filtration should be more than 90 %."Each inline filter should be placed in a separate casing to maintain integrity and shape of inline filters"Should confirms ISO 3826 and same should be reflect on Aluminium foil and labels. "The needle force should be less than 16 gram. "The lable should be hot marked Lable with barcode. "Company have market standing of more than 5 years | 40 | 1000 | NUMBER | 10000 |
| 23 . | 23 | M1 | 23 | 23/002/0035/00/0/0/0 | SGOT/AST. AST: IFCC KINETIC WITH PLP | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 49000 | MILILITER | 900 |
| 24 . | 24 | M1 | 24 | 23/002/0036/00/0/0/0 | SGPT/ALT. ALT: IFCC KINETIC WITH PLP | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 67000 | MILILITER | 1300 |
| 25 . | 25 | M1 | 25 | 23/003/0001/00/0/0/0 | LDL CHOLESTEROL BY DIRECT METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 5000 | MILILITER | 1300 |
| 26 . | 26 | M1 | 26 | 23/003/0003/00/0/0/0 | S.AMYLASE TEST KIT CNP-G3 KINETIC METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 25 ML | 40 | 4500 | MILILITER | 800 |
| 27 . | 27 | M1 | 27 | 23/003/0004/00/0/0/0 | S.URIC ACID TEST KIT URICASE PEROXIDASE END POINT | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 100 ML | 40 | 7200 | MILILITER | 200 |
| 28 . | 28 | M1 | 28 | 23/003/0005/00/0/0/0 | TRIGLYCERIDES ENZYMATIC,END POINT | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 11500 | MILILITER | 800 |
| 29 . | 29 | M1 | 29 | 23/003/0006/00/0/0/0 | S.BILIRUBIN TEST KIT TOTAL & DIRECT, JENDRASSIK & GROF\S METHOD | END POINT THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 65000 | MILILITER | 400 |
| 30 . | 30 | M1 | 30 | 23/003/0007/00/0/0/0 | S.CRETININE TEST KIT ALKALINE PICRATE FIX TIME KINETIC METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 48000 | MILILITER | 300 |
| 31 . | 31 | M1 | 31 | 23/003/0008/00/0/0/0 | HDL-CHOLESTEROL DIRECT HOMOGENOUS METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 10000 | MILILITER | 1800 |
| 32 . | 32 | M1 | 32 | 23/003/0009/00/0/0/0 | S.PHOSPHEROUS TEST KIT MOLYBDATE AT 340nm WITHOUT REDUCING AGENT | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 50 ML | 40 | 6600 | MILILITER | 100 |
| 33 . | 33 | M1 | 33 | 23/003/0013/00/0/0/0 | URINE PREGNANCY TEST KIT ( STRIP ) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 7000 | TEST | 300 |
| 34 . | 34 | M1 | 34 | 23/003/0014/00/0/0/0 | GLUCOSE TEST KIT ENZYMATIC GLUCOSE OXIDASE PEROXIDASE METHOD | END POINT THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 500 ML | 40 | 70000 | MILILITER | 400 |
| 35 . | 35 | M1 | 35 | 23/003/0015/00/0/0/0 | BLOOD UREA TEST KIT BERTHLOT METHOD END POINT | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 2400 | MILILITER | 100 |
| 36 . | 36 | M1 | 36 | 23/003/0016/00/0/0/0 | A.S.O.TEST KIT | RAPID SLIDE TEST,POSSITIVE & NEGATIVE CONTROL & NECESSARY ACCESSERIES NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 3500 | TEST | 300 |
| 37 . | 37 | M1 | 37 | 23/003/0017/00/0/0/0 | R.A. TEST KIT | RAPID SLIDE AGGLUTINATION TEST METHOD WITH POSSITIVE & NEGATIVE CONTROLS & NECESSARY ASSECCERIES NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 6000 | TEST | 400 |
| 38 . | 38 | M1 | 38 | 23/003/0018/00/0/0/0 | C.R.P. TEST KIT | LATEX AGGLUTINATION TEST WITH CONTROL & NECESSARY ACCESSRIES NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 100 TEST | 40 | 11500 | TEST | 600 |
| 39 . | 39 | M1 | 39 | 23/003/0023/00/0/0/0 | GLUCOSE 6 PHOSPHATE DEHYDROGENASE(1) SCREENING (G.6.P.D SINGLE TEST | VIAL & TEST TO BE COUNTED T IN 11/2 TO 1 HOURS THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 10 TEST | 40 | 6500 | TEST | 1900 |
| 40 . | 40 | M1 | 40 | 23/003/0025/00/0/0/0 | LACTATE DEHYDROGENASE KINETIC AT UV RANGE | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 30 ML | 40 | 6000 | MILILITER | 200 |
| S.NO | TenderItemID | Store Code | Item Serial | ItemCode | Item Name | Specification | DelDays | Quantity | Unit Description | EMD RS. |
| 1 . | 41 | M1 | 41 | 23/003/0026/00/0/0/0 | HIGH DENCITY LIPO PROTEIN CHLOLESTROL(HDL CHOL) PRECIPITANT WITH | PHOSPHOTUNGSTIC ACID AND MEGNESIUM CHLORIDE WITHOUT CHOLESTROL ESTIMATING REAGENT THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 75 ML | 40 | 2000 | MILILITER | 100 |
| 2 . | 42 | M1 | 42 | 23/003/0030/00/0/0/0 | FIBRINOGEN KIT | (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION FOR FIBRINOGEN(2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP(5) CE MARK, ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHOULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FIBRINOGEN IN CASES OF DIC NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 20 TEST | 40 | 1020 | TEST | 1300 |
| 3 . | 43 | M1 | 43 | 23/003/0031/00/0/0/0 | FIBRIN DEGRADATION PRODUCT KIT (FDP) | (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION OF FIBRIN DEGRADATION PRODUCTS (2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP (5) CE MARK,ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FDP IN CASES OF DIC NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 20 TEST | 40 | 900 | TEST | 1600 |
| 4 . | 44 | M1 | 44 | 23/003/0033/00/0/0/0 | HIV RAPID TEST (WITHOUT ELIZA READER) | SHOULD DETECT HIV-1 & HIV-2 SEPERATELY, SHOULD HAVE INTERNAL COTROL, SHOULD BE BASED ON CASSETTE METHOD NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 16000 | TEST | 3000 |
| 5 . | 45 | M1 | 45 | 23/003/0034/00/0/0/0 | ACTIVATED PARTIAL PROTHOMBIN TIME (APTT) KIT | READY TO USE WITH LONG EXPIRY DATE NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 2 ML | 40 | 4100 | MILILITER | 2800 |
| 6 . | 46 | M1 | 46 | 23/003/0035/00/0/0/0 | A.S.O. TEST KIT (QUNTITATIVE / TURBIDOMETRY) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 100 | TEST | 100 |
| 7 . | 47 | M1 | 47 | 23/003/0036/00/0/0/0 | R.A. TEST KIT (QUNTITATIVE / TURBIDOMETRY) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 100 | TEST | 100 |
| 8 . | 48 | M1 | 48 | 23/003/0037/00/0/0/0 | C.R.P. TEST KIT (QUNTITATIVE / TURBIDOMETRY) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 1300 | TEST | 300 |
| 9 . | 49 | M1 | 49 | 23/003/0038/00/0/0/0 | RAPID PAP STAIN KIT OF 250 TEST | (1) ONE KIT SHOULD STAIN ATLEAST 250 SMEARS. (2) STAIN SHOULD BE COMPLETED WITHIN 3 MIN.(3) IT SHOULD CONTAIN- NUCLEAR STAIN- CYTOPLASMIC STAIN- OG-65 SOLUTION- LIGHT GREEN SF EOSIN- BIO-FIX SPARY- DPX- XYLENE- WASH BUFFER (4) IT SHOULD GIVE COMPARABLE RESULT WITH USUAL PAP STAIN IT IS MUST FOR REPORTING OF GYNAC SMEAR, OTHER CYTOLOGY SMEAR AND MASS CYTOLOGY SCREENING CAMP | 40 | 100 | KIT Of 250 TEST | 800 |
| 10 . | 50 | M1 | 50 | 23/003/0040/00/0/0/0 | BRAIN THROMBOPLASTIN (PROTHOMBINTIME TEST KIT) | NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 4 ML | 40 | 4300 | MILILITER | 2000 |
| 11 . | 51 | M1 | 51 | 23/003/0041/00/0/0/0 | CSF PROTEIN/URINARY PROTEIN BY PYROGALLO RED DIE BINDING METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 100 ML | 40 | 3000 | MILILITER | 100 |
| 12 . | 52 | M1 | 52 | 23/003/0042/00/0/0/0 | WIDAL ANTIGEN SETS (SLIDE AGGLUTINATION ANTIGEN TEST) | WIDAL AGGLUTINATION ANTIGENS O,H,AH,BH (4 AGX5ML) POSSITIVE CONTROL IS TO BE PROVIDED WITH ACCESSORIES | 40 | 2800 | MILILITER | 300 |
| 13 . | 53 | M1 | 53 | 23/003/0044/00/0/0/0 | HBs AG RAPID KIT | TO REFER TECHNICAL BID FOR SPECIFICATION"Should be FDA/CE/WHO certified company."The assay should have solid phase/particles coated with monoclonal antibodies to HBsAg. "Sensitivity -: should be more than 99 %."Specificity -: More than 99 % (against whole HBsAg antigen) "Should have minimum chance of cross reactivity." Detect all the 11 subtypes of HBsAg and mutant strain. "Should have minimum indertminant result. Inter reader variability should be near to zero."Shelf life -: Minimum nine months."The pack size of the kit shall not be more than 50 Tests, wherein each device should be individually packed."Sensitivity & Specificity should be determined by WHO/Government authority."Company should provide the trace record for temprature maintainance during storage and transport."The control should be able to detect human immunoglobulin and should not be just "procedural control" or meant for merely checking the flow of reagents or the integrity of the antigen. | 40 | 13000 | TEST | 1100 |
| 14 . | 54 | M1 | 54 | 23/003/0045/00/0/0/0 | WIDAL TUBE TEST FOR S.TYPHI O,H & PARATYPHI AH, BH(PACK SIZE 4X50ML) | - | 40 | 1100 | TEST | 200 |
| 15 . | 55 | M1 | 55 | 23/003/0046/00/0/0/0 | WIDAL TUBE TEST FOR S. TYPHI O,H (PACK SIZE: 2+2X50ML) | - | 40 | 1100 | TEST | 200 |
| 16 . | 56 | M1 | 56 | 23/003/0047/00/0/0/0 | BLOOD UREA UREASE, GLDH FIXED TIME KINETIC METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 60000 | MILILITER | 1200 |
| 17 . | 57 | M1 | 57 | 23/003/0048/00/0/0/0 | ALKALINE PHOSPHATASE WITH PNPP SUBSTRATE WITH AMP BUFER | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 38000 | MILILITER | 1700 |
| 18 . | 58 | M1 | 58 | 23/003/0049/00/0/0/0 | DENGUE ELISA NS 1 KIT, FOR DENGUE DETECTION OF NS1 ELISA | - | 40 | 192 | TEST | 200 |
| 19 . | 59 | M1 | 59 | 23/003/0051/00/0/0/0 | HAV IgM ELISA KIT, FOR HEPATITIS A VIRUS TESTING | - | 40 | 960 | TEST | 500 |
| 20 . | 60 | M1 | 60 | 23/003/0052/00/0/0/0 | HEV IgM ELISA KIT, FOR HEPATITIS E VIRUS TESTING | - | 40 | 960 | TEST | 500 |
| 21 . | 61 | M1 | 61 | 23/003/0053/00/0/0/0 | CHOLESTEROL ENZYMATIC, END POINT | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 12000 | MILILITER | 300 |
| 22 . | 62 | M1 | 62 | 23/003/0054/00/0/0/0 | CPK-MB IMMUNOINHIBITION UV METHOD WITH HUMAN SERUM BASED CONTROL ONLY | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 5300 | MILILITER | 1300 |
| 23 . | 63 | M1 | 63 | 23/003/0055/00/0/0/0 | CPK TOTAL. CPK: NAC ACTIVATED UV METHOD | This criteria is common for all kits.The manufacturer should have ISO: 13485 certification for the reagents, kits with date of validity. Also manufacturer/Tenderer should provide the validation data report for the kits supplied, from the original manufacturer as per ISO: 15189: 2007 or newer, for technical specification such as linearity, precision, accuracy, expressed as a measurement of uncertainty limit of detection, measurement, sensitivity and specificity and interference.This is to be provided for the lot number supplied to SMIMER, and to be updated for new batch number, if supplied. | 40 | 10250 | MILILITER | 1200 |
| 24 . | 64 | M1 | 64 | 23/003/0056/00/0/0/0 | MEASLES IgM ELISA KIT, FOR MEASLES VIRUS TESTING | - | 40 | 96 | TEST | 100 |
| 25 . | 65 | M1 | 65 | 23/003/0057/00/0/0/0 | SERUM ALBUMIN BCG METHOD | THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. NOTE : QUOTE THE RATE FOR 1 ML & PACK SIZE AT THE TIME OF DELIVERY IS 200 ML | 40 | 40000 | MILILITER | 300 |
| 26 . | 66 | M1 | 66 | 23/003/0058/00/0/0/0 | ANTI Hbc IgM ELISA KIT | - | 40 | 96 | TEST | 400 |
| 27 . | 67 | M1 | 67 | 23/003/0059/00/0/0/0 | TYPHOID IgM RAPID KIT | - | 40 | 2800 | TEST | 700 |
| 28 . | 68 | M1 | 68 | 23/003/0063/00/0/0/0 | HBeAG DETECTION ELISA METHOD KIT | - | 40 | 96 | TEST | 100 |
| 29 . | 69 | M1 | 69 | 23/003/0064/00/0/0/0 | HBsAg ELISA KIT | TO REFER TECHNICAL BID FOR SPECIFICATION"Should be FDA/CE/WHO certified company."Principle -: Qualitative enzyme immunoassay kit for the detection of (Hepatitis B surface antigen (Hbs Ag) in human serum or plasma."Sensitivity -: 100 %"Antigen sensitivity should be 0.05 ng/ml."Specificity -: More than or equal to 98 %."Assay time should not be more than 2 hours."Detects all the known 11 subtypes of HBV and also mutant strains."Shelf life -: minimum 9 months at the time of delivery."Pack size -: 96 Tests."Easy to use on automated and semi-automatic processor."Company will have to provide additional wash buffer and control if required."Sensitivity & Specificity should be determined by WHO/Government authority."company should provide the trace record for temprature maintainance during storage and transport. | 40 | 13152 | TEST | 1600 |
| 30 . | 70 | M1 | 70 | 23/003/0065/00/0/0/0 | MALARIA ELISA KIT | Samples within a short time frame. Sensitivity and specificity of a histidine-rich protein 2 (HRP2)-based and plasmodium Lacted Dihybroginose (PLDH) based. Shelf life - Minimum 1 Year.Sensitivity 100% & Specificity 100% .Timing for procedure should be minimum | 40 | 7008 | TEST | 1400 |
| 31 . | 71 | M1 | 71 | 23/003/0068/00/0/0/0 | DENGUE ELISA DETECTION OF IgM CAPUR ELISA | QUALITATIVE DETECTION OF DENGUE VIRUS SPECIFIC IgM ANTIBODIES IN SERUM/PLASMA OR CsF FOR LABORATORY DIAGNOSIS OF THE DENGUE KIT SHOULD BE COMPATIBLE WITH FULLY AUTOMATIC ELISA READER WITH ADDITIONAL WASH-BUFFER ATLEAST ONE (1) BOTTLE WITH EACH KIT | 40 | 960 | TEST | 900 |
| 32 . | 72 | M1 | 72 | 23/003/0069/00/0/0/0 | DENGUE RAPID KIT (TO DETECT NS1 ANTIGEN, IgM, IgG ANTIBODIES | - | 40 | 1200 | TEST | 1100 |
| 33 . | 73 | M1 | 73 | 23/003/0092/00/0/0/0 | MYLOPEROXIDASE KIT | - | 40 | 2 | KIT | 800 |
| 34 . | 74 | M1 | 74 | 23/003/0093/00/0/0/0 | PLATLET PGD TEST | BY ELISA METHOD * SHOULD BE DETECT BROAD RANGE OF BACTERIA IN PLATLETS * REPRODUCIBILITY SHOULD BE > 99.80% * SPECIFICITY SHOULD BE > 98% * HAVE CONTROL (NAGATIVE & POSSITIVE) * SHOULD PROVIDE ACCESSORIES (TRAY,TUBE, PIPETTE ETC.) | 40 | 20 | TEST | 100 |
| 35 . | 75 | M1 | 75 | 23/003/0095/00/0/0/0 | HIV ELISA KIT 4TH GENERATION METHOD | TO REFER TECHNICAL BID FOR SPECIFICATION"Should be FDA/CE/WHO certified company."Principle -: Qualitative enzyme immunoassay kit for the detection of HIV-1 , HIV-2 antibodies & antigen p24. "Use of gp41, gp120, gp36 antigen & Monoclonal antibodies to p24."Assay time should not more than 03 hours."Reagent should be stable after dilution."Ready to use reagent is prefer."Separate positive control for antigen & antibody will be preferred."Analytic sensitivity for p24 antigen should be 8 IU/ml or 41 pg/ml. "Sensitivity -: 100 %"Specificity -: More than 98 %"Self life -: Minimum 9 months at the time of delivery."Pack size -: 96 Tests."Easy to use on automated and semi-automatic processor."Company will have to provide additional wash buffer and control if required."Sensitivity & Specificity should be determined by WHO/Government authority."company should provide the trace record for temprature maintainance during storage and transport. | 40 | 12960 | TEST | 2700 |
| 36 . | 76 | M1 | 76 | 23/003/0098/00/0/0/0 | TPHA ELISA KIT ( IgG + IgM ) | TO REFER TECHNICAL BID FOR SPECIFICATION"Should be FDA/CE/WHO certified company."Principle-: Qualitative enzyme immunoassay kit for the detection of Treponema Pallidum Antibodies (IgM, IgA & IgG) in human serum or plasma."Sensitivity-: 100%"Specificity-:100%"Shelf Life-: More than one year."Pack size-: 96 tests"Easy to use on automated and semi-automatic processor."Sensitivity & Specificity should be determined by WHO/Government authority."company should provide the trace record for temperature maintenance during storage & transport. | 40 | 12960 | TEST | 2400 |
| 37 . | 77 | M1 | 77 | 23/003/0099/00/0/0/0 | CRYPTOCOCCAL ANTIGENT DETECTION TEST LATEX | - | 40 | 20 | TEST | 100 |
| 38 . | 78 | M1 | 78 | 23/003/0100/00/0/0/0 | TPHA KIT FOR Tp ANTIBODY DETECTION, BASED ON HA | - | 40 | 100 | TEST | 100 |
| 39 . | 79 | M1 | 79 | 23/003/0101/00/0/0/0 | SICKLING TEST (READY TO USE BASED ON QUALITATIVE SOLUBILITY TEST) | NOTE : QUOTE THE RATE FOR 1 TEST & PACK SIZE AT THE TIME OF DELIVERY IS 50 TEST | 40 | 3500 | TEST | 700 |
| 40 . | 80 | M1 | 80 | 23/003/0111/00/0/0/0 | EXTRACTION KIT FOR RNA SPIN COLUMNS BASED | - | 40 | 9000 | TEST | 16200 |
| S.NO | TenderItemID | Store Code | Item Serial | ItemCode | Item Name | Specification | DelDays | Quantity | Unit Description | EMD RS. |
| 1 . | 81 | M1 | 81 | 23/003/0112/00/0/0/0 | PCR KIT COVID-19, MULTIPLEXING RT-PCR KIT, ICMR APPROVED | FOR SPECIFICATION REFER TECHNICAL BID REAL TIME THERMAL CYCLER (RTPCT)1.Should be automated system for real time PCR and Post PCR analysis- Critical2.Should be an open system real time PCR assay system with peltier / air based technology for heating and cooling - Critical3.Should be standardized for Taqman and Syber green chemistry. - Critical4.Should support the following applications a. Absolute quantification- Criticalb. Relative quantification - Criticalc. Multiplex PCR- Criticald. Dissociation curve analysis- Criticale. Melt curve analysis- Criticalf. Alleleie discrimination- Criticalg. HRM - Critical5.Should allow normalization of reactions due to non PCR related fluctuations by addition of any passive reference calibrated dye of optional or should be provided by the hardware itself.- Critical6.Thermal Block / Rotor - (a) 96 wells / 72 well rotor, should support 0.2ml / 0.1 ml optical PCR tubes- Critical7.Temperature range of 30?C to 99?C- Critical8.Should provide a RAMP rate of 2-5 deg. C per sec. - Critical9.Should be able to support hot start PCR cycle.- Critical10.System should support a reaction volume from 10 to 30?l. - Critical11.Optics - Excitation by tungsten halogen lamp or LED or Xenon lamp and detection by CCD cameras/ photodiodes/PMT- Critical12.Should have six fluorescence excitation and emission filters and data should be collected for all filters for all wells.- Critical13.Platform should provide following calibrated dyes at installation-SYBR green, FAM,VIC, JOE, NED, TAMRA, Cy-3, and Texas red, Cy-5. Should offer flexibility in selection of dye for each filter. - Critical 14.Dedicated licensed full version software must be included in the supply. - Critical15.Platform should be IVD certified - Critical16.Analysis Software and computer / laptop having Microsoft system and relevant analysis software must be provided with the system. - Critical17.Calibration or validation plates should be provided wherever applicable.- Critical18.Power in put to be 220-240V, 50Hz.- Critical19.CE marked / FDA approved. - Critical20.Suitable online UPS of two hours should be provided- Critical | 40 | 9000 | TEST | 72000 |
| 2 . | 82 | M1 | 82 | 23/003/0113/00/0/0/0 | UREASE TEST KIT, FOR H PYLORI | - | 40 | 300 | KIT | 7200 |
| 3 . | 83 | M1 | 83 | 23/004/0131/00/0/0/0 | RETRACTILE, SINGLE USE SAFETY LANCET FOR CAPILLARY BLOOD COLLECTION | FOR SPECIFICATION REFER TECHNICAL BID RETRACTILE, SINGLE USE SAFETY LANCET FOR CAPILLARY BLOOD COLLECTIONUS FDA CERTIFICATE,ISO / CE CERTIFICATE,SINGLE TIME USEABLE LANCET WITH NEEDLE 23 G X DEPTH 1.8 MM,STERILE ( GAMA / ETO ),MADE OF PET MATERIAL,SAFETY TIP CLOSURE, AUTO LOCK BUTTON,AUDIBLE CLICK,BATCH-WISE STERILITY / NON-PYROGENICITY / NON-TOXICITY CERTIFICATE,ADEQUATE COMBUSTION DATA TO PROVE THAT IT IS SAFE FOR THE ENVIRONMENT UPON,5 YEARS MANUFACTURING LICENSE FOR EVACUATED BLOOD COLLECTION TUBE, FROM THE SUPPLIERS,PROOF OF SUPPLY TO AT LEAST THREE GOVERNMENT INSTITUTES / HOSPITALS,INSTRUMENT COMPATIBILITY CERTIFICATES FROM VARIOUS INSTRUMENT MANUFACTURERS,AT LEAST 100 SAMPLES OF EACH TYPE OF TUBE SHOULD BE PROVIDED WITH THE TENDERS,EXPIRY SHOULD BE MINIMUM OF 6 MONTHS,SEE SPECIFICATION IN TECHINICAL BID. | 40 | 8000 | NUMBER | 600 |
| 4 . | 84 | M1 | 84 | 23/004/0132/00/0/0/0 | VACCUMIZED TUBE WITH SPRAY DRIED K2 EDTA WITH PINK COLOR CAP | FOR SPECIFICATION REFER TECHNICAL BID. VACCUMIZED TUBE WITH SPRAY DRIED K2 EDTA WITH PINK COLOR CAP FOR BLOOD GROUPING OR CROSS MATCH ( NEW SPECIFICATION ),US FDA CERTIFICATE,ISO / CE CERTIFICATE,VOLUME 2 ML,TUBE SIZE 13 X 75 MM,STERILE ( GAMA / ETO ),MADE OF PET MATERIAL,SAFETY CAP CLOSURE,QUANTITATIVE ADDITIVE INFORMATION ON EACH TUBE LABEL,TUBES MAKING AS PER NCCLS / CLSI GUIDELINE,BATCH-WISE STERILITY / NON-PYROGENICITY / NON-TOXICITY CERTIFICATE,ADEQUATE COMBUSTION DATA TO PROVE THAT IT IS SAFE FOR THE ENVIRONMENT UPON INCINERATION,5 YEARS MANUFACTURING LICENSE FOR EVACUATED BLOOD COLLECTION TUBE, FROM THE SUPPLIERS,PROOF OF SUPPLY TO AT LEAST THREE GOVERNMENT INSTITUTES / HOSPITALS,INSTRUMENT COMPATIBILITY CERTIFICATES FROM VARIOUS INSTRUMENT MANUFACTURERS,AT LEAST 100 SAMPLES OF EACH TYPE OF TUBE SHOULD BE PROVIDED WITH THE TENDERS,EXPIRY SHOULD BE MINIMUM OF 6 MONTHS,SEE SPECIFICATION IN TECHINICAL BID. | 40 | 15000 | NUMBER | 1400 |
| 5 . | 85 | M1 | 85 | 23/004/0133/00/0/0/0 | VACCUMIZED TUBES FOR ACD SOLUTION | FOR SPECIFICATION REFER TECHNICAL BID. VACCUMIZED TUBES FOR ACD SOLUTION A : ( TRISODIUM CITRATE (2.59 MG/ML),CITRIC ACID (0.94 MG/ML),DEXTROSE (2.88 MG/ML),POTASSIUM SORBATE (0.024 MG/ML),U S FDA CERTIFICATE,ISO / CE CERTIFICATE,VOLUME 8.5 ML,TUBE SIZE 16 X 100 MM,STERILE ( GAMA / ETO ),MADE OF GLASS MATERIAL,RUBBER CAP CLOSURE,BATCH-WISE STERILITY / NON-PYROGENICITY / NON-TOXICITY CERTIFICATE,ADEQUATE MBUSTION DATA TO PROVE THAT IT IS SAFE FOR THE ENVIRONMENT UPON INCINERATION,5 YEARS MANUFACTURING LICENSE FOR EVACUATED BLOOD COLLECTION TUBE, FROM THE SUPPLIERS,PROOF OF SUPPLY TO AT LEAST THREE GOVERNMENT INSTITUTES / HOSPITALS,INSTRUMENT COMPATIBILITY CERTIFICATES FROM VARIOUS INSTRUMENT MANUFACTURERS,AT LEAST 100 SAMPLES OF EACH TYPE OF TUBE SHOULD BE PROVIDED WITH THE TENDERS,EXPIRY SHOULD BE MINIMUM OF 6 MONTHS,SEE SPECIFICATION IN TECHINICAL BID. | 40 | 300 | NUMBER | 100 |
| 6 . | 86 | M1 | 86 | 23/004/0135/00/0/0/0 | EDTA(1 MG )MICROCONTAINER BLOOD COLECTION TUBES FOR NEONENTAL | FOR SPECIFICATION REFER TECHNICAL BID. EDTA (1 MG ) MICROTAINER BLOOD COLLECTION TUBES COLLECTED FORM CAPILLARY OR VEIN FROM PAEDIATERIC / NEONENTAL,U S FDA CERTIFICATE,ISO / CE CERTIFICATE,VOLUME 0.5 ML,STERILE ( GAMA / ETO ),MADE OF PET MATERIAL,SAFETY CAP CLOSURE,BATCH-WISE STERILITY / NON-PYROGENICITY / NON-TOXICITY CERTIFICATE,ADEQUATE COMBUSTION DATA TO PROVE THAT IT IS SAFE FOR THE ENVIRONMENT UPON INCINERATION,5YEARS MANUFACTURING LICENSE FOR EVACUATED BLOOD COLLECTION TUBE, FROM THE SUPPLIERS,PROOF OF SUPPLY TO AT LEAST THREE GOVERNMENT INSTITUTES / HOSPITALS,INSTRUMENT COMPATIBILITY CERTIFICATES FROM VARIOUS INSTRUMENT MANUFACTURERS,AT LEAST 100 SAMPLES OF EACH TYPE OF TUBE SHOULD BE PROVIDED WITH THE TENDERS,EXPIRY SHOULD BE MINIMUM OF 6 MONTHS, SEE SPECIFICATION IN TECHINICAL BID. | 40 | 2200 | NUMBER | 200 |
| 7 . | 87 | M1 | 87 | 23/005/0101/00/0/0/0 | HIV RAPID TEST KIT (IC) | SHOULD DETECT HIV-1 & HIV-2 SEPRATELY, SHOULD HAVE INTERNAL CONTROL, SHOULD BE BASED ON COMB METHOD | 40 | 2100 | TEST | 500 |
| 8 . | 88 | M1 | 88 | 23/006/0053/00/0/0/0 | RAPID HIV Ag+Ab DETECTION KIT (4TH GENERATION ) | TO REFER TECHNICAL BID FOR SPECIFICATION"Should be FDA/CE/WHO certified company."Principle -: enzyme immunoassay based on \Sandwich Immunoassay\ HIV antigens and p24 antibody is Immobilized on a porous immunofiltration membrane."Sensitivity should be 100 %"Specificity should be 100 %" Use of Antigen gp-41, terminus of gp-120 for HIV-1antibodies and gp-36 for HIV-2 antibodies."Rapid visual sensitive & qualitative in vitro diagnostic Test."Should have minimum chance of cross reactivity."Should have superior sensitivity of test."Should have two separate dot for HIV 1 & 2 .One for p24 antigen & one for control."Sensitivity & specificity should be evaluated by WHO/Gov.authority."Based on flow through technology."Clear interpretation of report. Should have minimum indertminet result .Inter reader variability should be near to zero."Self life -: More than one year."Pack size -: 20 to 50 Test/kit."Sensitivity & Specificity should be determined by WHO/Government authority."company should provide the trace record for temprature maintainance during storage and transport. | 40 | 1100 | TEST | 1600 |
| 9 . | 89 | M1 | 89 | 23/006/0111/00/0/0/0 | LEUKOCYTE ALKALINE PHOSPHATASE (LAP SCORE KIT) | READY TO USE KIT, ONE KIT SHOULD STAIN ATLEAST 300 SLIDES FOR DIAGNOSIS OF LEUKEMIA | 40 | 1 | KIT | 100 |
| 10 . | 90 | M1 | 90 | 25/001/0041/00/0/0/0 | PT VACUTAINER (PROTHROMBIN TIME TEST) | VACCUM BLOOD COLLECTION TUBE WITH CITRATE, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, 2.7ML BLOOD + 0.3ML TSC 3.2% ISO, ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE | 40 | 37000 | NUMBER | 1000 |
| 11 . | 91 | M1 | 91 | 25/003/0006/00/0/0/0 | EDTA VACUTAINER | VACCUM BLOOD COLLECTION TUBE K2-EDTA, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE | 40 | 275000 | NUMBER | 7100 |
| 12 . | 92 | M1 | 92 | 25/003/0007/00/0/0/0 | FLUORIDE VACUTTE (EVACUATED PET TUBE WITH NA FLUORIDE 2ML CAP.) | VACCUM BLOOD COLLECTION TUBE K2-EDTA & NA FLUORIDE 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE | 40 | 125000 | NUMBER | 3300 |
| 13 . | 93 | M1 | 93 | 25/003/0008/00/0/0/0 | PLAIN VACUTTE (PLAIN PET TUBE WITH CLOT ACTIVATOR& POLYEMER GEL 5MLCAP | VACCUM BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 5ML FITTED WITH COLOURED CAP, MADE OF PET, WITH CLOT ACTIVATER ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE | 40 | 350000 | NUMBER | 9000 |
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