}

Supply Of Laboratory Items - Total Item No 1 To 2316(Part 1:- Item No 1 To 350)- Pro-Clacitonin,Ferritin,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1 & B,Ceruloplasmin,Hep, Vadodara-Gujarat

Health And Family Welfare Department has published Supply Of Laboratory Items - Total Item No 1 To 2316(Part 1:- Item No 1 To 350)- Pro-Clacitonin,Ferritin,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1 & B,Ceruloplasmin,Hep. Submission Date for this Tender is 17-08-2023. Laboratory Electrophoresis and Blotting System Tenders in Vadodara Gujarat. Bidders can get complete Tender details and download the document.




Tender Notice

38614137
Corrigendum : Supply Of Laboratory Items - Total Item No 1 To 2316(Part 1:- Item No 1 To 350)- Pro-Clacitonin,Ferritin,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1 & B,Ceruloplasmin,Hep
Open Tender
Indian
Gujarat
Vadodara
17-08-2023

Tender Details

Supply Of Laboratory Items - Total Item No 1 To 2316(Part 1:- Item No 1 To 350)- Pro-Clacitonin,Ferritin,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1 & B,Ceruloplasmin,Heptoglobin,Bnp,Lipoprotein A,Insulin,Pth,Vitamin D,Zinc,Ammonia,Total Iron,Hs-Crp,Pro-Clacitonin,Il-6,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1,Apo-Lipoprotein B,Ceruloplasmin,Heptoglobin,Lipoprotein A,Transferrin,Galactin-3,Estradiol,Progesterone,Prolactin,Amh,Testosterone,C-Peptide,Cortisol,Insulin,Pth,Vitamin D3,Tsh,Free T4,Free T4,Anti- Tpo,Lactate,Fructosamine,Uibc,Tibc,Psa (Total),Psa (Free),Fsh,Lh,Leptin,Adiponectine,Zinc,Inhibin,Ca 27.29,Ca 15.3,Ca 19-9,Cea,Ca 125,Afp,Cystatin C,Bnp,Transferrin,Galactin-3,Estradiol,Progesterone,Prolactin,Amh,Testosterone,C-Peptide,Cortisol,Insulin,Pth,Vitamin D,Free T3,Free T4,Lactate,Fructosamine,Uibc,Tibc,Psa (Total &Free),Fsh,Lh,Leptin,Adiponectine,Zinc,Ammonia,Measuring Cartridge,Wash Cartridge,Sample Cup,Auto Wash,Acid -Alkaline Wash,Cuvette,Cuvette,Reagent Bottle,Reagent Bottle,Reagent Bottle,Reagent Bottle,Cd-8 Wash Solution,Electrolyte Reagent Pack,Deproteinizer,Heparinized Glass Capillaries For Bill-P Bilirubinometer,Serum Iron Estimation Kit*,Serum Ferritin Estimation Kit*,Hank’S Balanced Salt Solution 10 X With Phenol Red Without Sodium Bicarbonate,D-Dimer (Quantitative Estimation Of D-Dimer Based On Turbidimetric Immunoassay. R1 & R2 Liquid Reagent , Measuring The Range Of 200-4000 Ng/Ml, Linearity 10000 Ng/Ml,Hb-Sensor Unit,Hb-Sensor Casing,Photo-Electric Sensor Device(Ls),Device For Specimen Input (Ds),Waste Bottle Sensor Device With Cable,Plasma Glucose Estimation Kit Based On God-Pod Enzymatic End €“ Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Plasma Glucose Estimation Kit Based On Hexokinase Enzymatic Uv Method (2 Point Analysis) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ferritin Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Urea Estimation Kit Based On Gldh Enzymatic Uv Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Urea Estimation Kit Based On Gldh Enzymatic Uv Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Urea Estimation Kit Based On Modified Berthelot Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Cholesterol Estimation Kit Based On Chod-Pod Enzymatic End €“ Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Creatinine Estimation Kit Based On Jaffe’S Method 2-Point Rate Reaction (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Creatinine Estimation Kit Based On Enzymatic Method(Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Protein Estimation Kit Based On Biuret Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Albumin Estimation Kit Colorimetric B.C.G. Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total And Direct Bilirubin Estimation Kit Based On Jendrassik & Grof Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total And Direct Bilirubin Estimation Kit Based On Jendrassik & Grof Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Bilirubin Estimation Kit For Fully Automated Biochemistry Analyzer (Single Reagent) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Direct Bilirubin Estimation Kit For Fully Automated Biochemistry Analyzer (Single Reagent) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Alp (Alkaline Phosphatase) Estimation Kit, Amp ( 2-Amino 2-Methyl 1-Propanol ) Buffer, Based On Ifcc Optimised Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Alp (Alkaline Phosphatase) Estimation Kit, Dea ( Diethanolamine ) Buffer (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Sgot Estimation Kit Based On Ifcc Optimised Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Sgpt Estimation Kit Based On Ifcc Optimised Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ck-Mb Estimation Kit Based On Ifcc Kinetic Method (Immunoinhibition) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Ck Estimation Kit Based On Ifcc Uv Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ldh Estimation Kit Based On Ifcc Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ggt Estimation Kit Based On Ifcc Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Hdl Precipitation Reagent Based On Polyethylene Glycol (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Hdl Estimation Kit Direct Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ldl Estimation Kit Direct Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Triglyceride Estimation Kit Based On Gpo-Pap Enzymatic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Calcium Estimation Kit Based On Arsenazo Iii Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Calcium - Ocpc Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Phosphorus Estimation Kit Based On Phospho-Molybdate Uv End Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Chloride Estimation Kit Based On Mercuric Thiocyanate Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Magnesium Estimation Kit Based On Xylidyl Blue Colorimetric End Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Bicarbonate Estimation Kit Based On Colorimetric Uv End Point/Fixed Time Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Alpha(A) Amylase Estimation Kit Based On Enzymatic Kinetic (Ifcc) Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Lipase Estimation Kit Based On Enzymatic Kinetic (Ifcc) Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Uric Acid Estimation Kit Based On Uricase-Pod End Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Micro Protein Estimation Kit For Determination Of Protein In Urine & Csf Based On Pyrogallol Red End-Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Fructosamine Estimation Kit Based On Nbt Kinetic Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Total Iron Estimation Kit Based On Ferrozine Colorimetric End Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Copper Estimation Kit Based On Colorimetric End Point Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hdl-Ldl Cholesterol Calibrator (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Ck-Mb Calibrator (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Ck-Mb Control Set (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Bilirubin Standard (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Bilirubin Standards Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Chemistry Standards Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Blood Gas Controls €“ Pack Of Normal And Abnormal Level (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Blood Gas Controls €“Abnormal Level (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Fructosamine Calibrator (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Sampling Precision Test Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Reagent Precision Test Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Quality Control Serum (Normal Level) (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature ),Quality Control Serum (Pathological- Higher Level) (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature ),Quality Control Serum (Pathological- Lower Level) (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature ),Multicalibrator Sera For Clinical Chemistry Assays (Normal Level) (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature),Multicalibrator Sera For Clinical Chemistry Assays (Higher Level) (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature),Multi-Parameter External Quality Assessment Scheme For Routine Clinical Chemistry Investigations (Vendor Must Provide Application Sheets / Msds And Protocol For Use Of Material. Temperature, Instrument And Method Specific Data, Values For All Tests In User Menu. Quote The Cost Per Ml Of The Reconstituted Liquid Material And Pack Size. Manufacturer Must Have All Quality Certifications Iso 13485 + Ce Mark + Us.Fda Attach Complete Kit Literature),Ammonia Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),C - Reactive Protein Calibrator Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),C - Reactive Protein Control Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Cholinesterase Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),G6 Pdh Estimation Kit (Quantitative) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Immunoturbidi Metric Kit For Hba1c (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hba1c Calibrator Set Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hba1c Control Set Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hemolysis Reagent For Immunoturbidi Metric Hba1c Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Homocysteine Calibrator Set Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Homocysteine Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Iga. Immunoglobulin A Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Igg. Immunoglobulin G Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Igm. Immunoglobulin M Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Immunoturbidi Metric Kit For C -Reactive Protein (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Immunoturbidi Metric Kit For Microalbumin (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Immunoturbidi Metric Kit For Pre Albumin (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Iron ( Total ) Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Lactate Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Micro-Albumin ( Micro-Protein ) In Csf / Serum / Urine Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Micro-Albumin Calibrator Set Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Micro-Albumin Controls Set Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Pancreatic Alpha Amylase Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Cystatin -C Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hba1c Estimation Kit For Fully Automated Biochemistry Analyzer (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hba1c Estimation Kit Based On Affinity Chromatography Method (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ferritin Kit (Latex Turbidimetry Method) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Total Iron Standard Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Uibc Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Zinc Estimation Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Hdl / Ldl Cholesterol Control Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Rapid Troponin-I Card Test (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Cassette For Detection Of Acute Myocardial Infarction (Troponin-I, Ck-Mb And Myoglobin) (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum T3 (Triiodothyronine) Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Free T3 (Free Triiodothyronine) Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum T4 (Thyroxin) Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Free T4 (Free Thyroxin) Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Tsh (Thyroid Stimulating Hormone) Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Preventive Maintenance (Pm) Kit For Erba Chem 5 Plus V2 Semiauto-Analyzer (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Anti-Tpo Antibodies Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ca-19.9 Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Alpha Feto Protein Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Beta-Hcg Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Psa Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Cea Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Fsh Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Lh Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Multi Assay Human Sera Based Tumour Marker Controls Kit For Laboratory Q.C. (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ca-125 Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Adiponectin Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Leptin Estimation Kit Based On Elisa (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Serum Ca-15.3 Estimation Elisa Kit (Attach Complete Kit Literature With Valid Iso 13485 & Ce Mark Or Us.Fda Certificate Of Kit Manufacturer ),Bees Wax,Tle 1,Pdl 1,Pax 5,Dog-1,Stat6,Nut,Muc 1,Muc5ac,Muc6,Muc4,Tfe3b,B72.3,Bcl10,Bcl6 Oncoprotein,Beta-Amyloid,Bg-8,Ca19-9,Cathepsin B,Cd3,Cd103,Cd11c,Cd123,Cd13,Cd138,Cd14,Cd19,Cd1a,Cd2,Cd22,Cd23,Cd24,Cd25,Cd33,Cd36,Cd38,Cd3-Epsilon Chain,Cd4,Cd43,Cd45,Cd45ra,Cd45ro,Cd61,Cd64,Cd7,Cd71,Cd9,Collagen Iv,Cytokerain18,D2-40,Eber,Ebv,Egfr,Epstein Barr Virus Early Antigen,Epstein-Barr Virus(Lmp),F13a,F8,Fl1,Gh,Glucagon,Glycophorin A,Growth Hormone,Hbme-1,Hbsag,Hemoglobin A,Hiv,P24,Hladr,Iga,Specific For Alpha-Chains,Igg,Specific For Gamma Chains,Igm,Specific For Mu-Chains,Imp3,Ini 1,Insulin,J Chain,Kappa Light Chains,Lambda Light Chains,Mammaglobin,Mast Cell Tryptase,Mitf,Moc-31,Muc2 Protein,Mum1 Protein,Myelin Basic Protein,Myod1,Napsina,Nestin,Oct--4,Pap(Prostatic Acid Phosphatase),P 16,Pcna,Pe-10,Plasma Cell (Clone Vs38c),Pp,Pr,Pten,Pth,Rcc,S-100,Somatostatin,Tia-1,Trap,Tryptase,Nkx3.1,Ez-Dewax Solution,Alpha - 1 - Antitrypsin,Alpha - 1 - Antichymotrypsin,Cd 13,Cd 14,Cd 16,Cdw 75,Ck 5,Ck8 & 18,Ck 14,Ck 15,Ck 16,Ck 17,Ck 18,Wt 1(Antibody To Carboxy Terminal),Epcam,Factor Viii Related Antigen,Factor Xiii A

Corrigendum Details

Sr No CorrigendumDate Corrignedum CorrigendumType NewSubmissionDate
1 31-Jul-2023 17-08-2023

Key Value

Document Fees
INR 5000 /-
EMD
INR 200000.0 /-
Tender Value
Refer document

BOQ Items

Sl. No.Item TitleSpecification
1Pro-ClacitoninBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
2ferritinBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
3D-dimerBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
4Vitamin B12Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
5Vitamin B3Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
6Troponin I & T (Quanitative)Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
7Beta HCGBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
8Beta 2 microglobulinBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
9Alpha 1 AntitrypsinBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
10Apo-Lipoprotein A1 & BBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
11CeruloplasminBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
12HeptoglobinBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
13BNPBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
14Lipoprotein ABased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
15InsulinBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
16PTHBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
17Vitamin DBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
18ZincBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
19AmmoniaBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
20Total IronBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
21hs-CRPBased on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
22Pro-ClacitoninAutomated Chemileuminisecence based Immunoassay test
23IL-6Automated Chemileuminisecence based Immunoassay test
24D-dimerAutomated Chemileuminisecence based Immunoassay test
25Vitamin B12Automated Chemileuminisecence based Immunoassay test
26Vitamin B3Automated Chemileuminisecence based Immunoassay test
27Troponin I & T (Quanitative)Automated Chemileuminisecence based Immunoassay test
28Beta HCGAutomated Chemileuminisecence based Immunoassay test
29Beta 2 microglobulinAutomated Chemileuminisecence based Immunoassay test
30Alpha 1 AntitrypsinAutomated Chemileuminisecence based Immunoassay test
31Apo-Lipoprotein A1Automated Chemileuminisecence based Immunoassay test
32Apo-Lipoprotein BAutomated Chemileuminisecence based Immunoassay test
33CeruloplasminAutomated Chemileuminisecence based Immunoassay test
34HeptoglobinAutomated Chemileuminisecence based Immunoassay test
35Lipoprotein AAutomated Chemileuminisecence based Immunoassay test
36TransferrinAutomated Chemileuminisecence based Immunoassay test
37Galactin-3Automated Chemileuminisecence based Immunoassay test
38EstradiolAutomated Chemileuminisecence based Immunoassay test
39ProgesteroneAutomated Chemileuminisecence based Immunoassay test
40ProlactinAutomated Chemileuminisecence based Immunoassay test
41AMHAutomated Chemileuminisecence based Immunoassay test
42TestosteroneAutomated Chemileuminisecence based Immunoassay test
43C-PeptideAutomated Chemileuminisecence based Immunoassay test
44CortisolAutomated Chemileuminisecence based Immunoassay test
45InsulinAutomated Chemileuminisecence based Immunoassay test
46PTHAutomated Chemileuminisecence based Immunoassay test
47Vitamin D3Automated Chemileuminisecence based Immunoassay test
48TSHAutomated Chemileuminisecence based Immunoassay test
49Free T4Automated Chemileuminisecence based Immunoassay test
50Free T4Automated Chemileuminisecence based Immunoassay test
51Anti- TPOAutomated Chemileuminisecence based Immunoassay test
52LactateAutomated Chemileuminisecence based Immunoassay test
53FructosamineAutomated Chemileuminisecence based Immunoassay test
54UIBCAutomated Chemileuminisecence based Immunoassay test
55TIBCAutomated Chemileuminisecence based Immunoassay test
56PSA (Total)Automated Chemileuminisecence based Immunoassay test
57PSA (Free)Automated Chemileuminisecence based Immunoassay test
58FSHAutomated Chemileuminisecence based Immunoassay test
59LHAutomated Chemileuminisecence based Immunoassay test
60LeptinAutomated Chemileuminisecence based Immunoassay test
61AdiponectineAutomated Chemileuminisecence based Immunoassay test
62ZincAutomated Chemileuminisecence based Immunoassay test
63InhibinAutomated Chemileuminisecence based Immunoassay test
64CA 27.29Automated Chemileuminisecence based Immunoassay test
65CA 15.3Automated Chemileuminisecence based Immunoassay test
66CA 19-9Automated Chemileuminisecence based Immunoassay test
67CEAAutomated Chemileuminisecence based Immunoassay test
68Ca 125Automated Chemileuminisecence based Immunoassay test
69AFPAutomated Chemileuminisecence based Immunoassay test
70Cystatin CAutomated Chemileuminisecence based Immunoassay test
71BNPCompatible with ELISA Reader and Washer.
72TransferrinCompatible with ELISA Reader and Washer.
73Galactin-3Compatible with ELISA Reader and Washer.
74EstradiolCompatible with ELISA Reader and Washer.
75ProgesteroneCompatible with ELISA Reader and Washer.
76ProlactinCompatible with ELISA Reader and Washer.
77AMHCompatible with ELISA Reader and Washer.
78TestosteroneCompatible with ELISA Reader and Washer.
79C-PeptideCompatible with ELISA Reader and Washer.
80CortisolCompatible with ELISA Reader and Washer.
81InsulinCompatible with ELISA Reader and Washer.
82PTHCompatible with ELISA Reader and Washer.
83Vitamin DCompatible with ELISA Reader and Washer.
84Free T3Compatible with ELISA Reader and Washer.
85Free T4Compatible with ELISA Reader and Washer.
86LactateCompatible with ELISA Reader and Washer.
87FructosamineCompatible with ELISA Reader and Washer.
88UIBCCompatible with ELISA Reader and Washer.
89TIBCCompatible with ELISA Reader and Washer.
90PSA (Total &Free)Compatible with ELISA Reader and Washer.
91FSHCompatible with ELISA Reader and Washer.
92LHCompatible with ELISA Reader and Washer.
93LeptinCompatible with ELISA Reader and Washer.
94AdiponectineCompatible with ELISA Reader and Washer.
95ZincCompatible with ELISA Reader and Washer.
96AmmoniaCompatible with ELISA Reader and Washer.
97Measuring CartridgeCompatible with ABG analyzer RAPID Point 500e
98Wash CartridgeCompatible with ABG analyzer RAPID Point 500e
99Sample CupCompatible with Fully Automated analyzer Erba XL- 640/ Mindray Bs-430
100Auto washCompatible with Fully Automated Analyzer Erba Xl-640
101Acid -Alkaline WashCompatible with Fully Automated Analyzer Erba Xl-640
102CuvetteCompatible with Fully Automated analyzer Erba XL- 640
103CuvetteCompatible with Fully Automated analyzer Mindray Bs-430
104Reagent Bottle20 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400
105Reagent Bottle40 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400
106Reagent Bottle20 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430
107Reagent Bottle40 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430
108CD-8 Wash SolutionCompatible with Fully Automated Analyzer Mindray BS-430
109Electrolyte Reagent PackCompatible with Acculyte 3P Electrolyte Analyzer
110DeproteinizerCompatible with Acculyte 3P Electrolyte Analyzer
111Heparinized Glass capillaries for Bill-P BilirubinometerCompatible with Bill-P Bilirubinometer
112Serum Iron estimation kit*Based on Ferrozine Colorimetric End Point Method, R1 & R2 reagent, liquid reagent,linearity 1000 µg/dI
113Serum Ferritin estimation kit*Based on Immunoturbidimetric method, R1 & R2 reagent,liquid reagent, linearity 600 µg/dI
114Hank’s Balanced Salt Solution 10 X With Phenol red without Sodium bicarbonateAs per Column no.2
115D-dimer (Quantitative estimation of D-dimer based on turbidimetric immunoassay. R1 & R2 liquid reagent , measuring the range of 200-4000 ng/ml, linearity 10000 ng/mlAs per Column no.2
116Hb-sensor unitOriginal
117Hb-sensor casingOriginal
118Photo-electric sensor device(LS)Original
119device for specimen input (DS)Original
120Waste bottle sensor device with cableOriginal
121Plasma GLUCOSE Estimation kit based on GOD-POD ENZYMATIC End – point method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid / Lypholysed Reagents.Adaptable to Endpoint 505 nm / Fixed time Kinetic method. GOD = 8 U/mL, Peroxidase = 0.6 U/L, Linearity = 500 mg/dL, Std : 100 mg/dL Sensitivity =1 mg/dL. CV < 2 %. Compatible to Semi Auto and Miura Fully Auto Analysers. Long expiry date & stability. Reagent stable for atleast 4 weeks after reconstitution.
122Plasma GLUCOSE Estimation kit based on HEXOKINASE ENZYMATIC UV Method (2 point analysis) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Hexokinase-UV-End Point 340 nm Method. Hexokinase>1500 U/L, G6PDH>3000 U/L, NAD>2mmol/L Linearity = 500 mg/dL Std :100 / 200 mg/dL CV < 5 %. Compatible with Miura Fully Auto + Semi Auto Analysers. Long expiry date & stability.
123Serum Ferritin Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
124Serum UREA Estimation Kit Based on GLDH ENZYMATIC UV KINETIC METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. GLDH UV-Kinetic Method. Urease>6000 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. %CV= 1. Compatible with Miura Fully Auto + Semi Auto Analysers.
125Serum UREA Estimation Kit Based on GLDH ENZYMATIC UV KINETIC METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. GLDH UV-Kinetic Method. Urease>6000 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. %CV= 1. Compatible with Miura Fully Auto + Semi Auto Analysers.
126Serum UREA Estimation Kit Based on MODIFIED BERTHELOT METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Modified Berthelot Method. Urease>4 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. CV < 1% Compatible with Miura Fully Auto + Semi Auto Analysers.
127Serum TOTAL CHOLESTEROL Estimation kit based on CHOD-POD ENZYMATIC End – point method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use, Single Reagent. Enzymatic - End Point 510 nm Method. Cholesterol Oxidase > 100 U / L., POD > 500 U / L., Linearity = 600 mg/dL. Sensitivity =4 mg/dL. %CV= 2 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry & stable reagents.
128Serum CREATININE Estimation Kit based on Jaffe’s Method 2-point rate reaction (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use & Single Reagent. Fixed-Rate 510 nm. Method Without Deproteinization.Picric acid = 9-10 mMol/L Standard : 2 mg / dL Linearity upto 20 mg/dL Sensitivity =0.2 mg/dL. %CV= 2. Compatible to Miura Fully Auto + Semi Auto Analysers.
129Serum CREATININE Estimation Kit based on Enzymatic method(Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use & Single Reagent. Fixed-Rate 510 nm. Method Without Deproteinization.Picric acid = 9-10 mMol/L Standard : 2 mg / dL Linearity upto 20 mg/dL Sensitivity =0.2 mg/dL. %CV= 2. Compatible to Miura Fully Auto + Semi Auto Analysers.
130Serum TOTAL PROTEIN Estimation Kit Based on BIURET Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready Use Single Reagent. Biuret - End Point 540 nm Method. Linearity: 15 Gm / dL Compatible with Miura Fully Auto + Semi Auto Analysers.
131Serum ALBUMIN Estimation Kit Colorimetric B.C.G. Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagent. Colorimetric 630 nm End-Point Method. Succinate Buffer. BromoCresolGreen > 0.15mmol / L Standard 5 G / dL. Linearity 0.2-6 G / dL Sensitivity 0.02 g/L. Compatible with Miura AutoAnalyser & Semi Auto analyzers.
132Serum TOTAL AND DIRECT BILIRUBIN Estimation kit based on JENDRASSIK & GROF Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use R1 & R2 Reagents. Colorimetric Diazo End Point 546 nm Jendrassik & Groff Method. Sulphanilic acid=5 mmol / L. Sufficient Nitrite Reagent. Two Point Calibrator within Kit. Onboard Stability of Working Reagents = 21 days. Linearity =25 mg/dL Sensitivity = 0.05 mg.% CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry date & stability.
133Serum TOTAL AND DIRECT BILIRUBIN Estimation kit based on JENDRASSIK & GROF Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use R1 & R2 Reagents. Colorimetric Diazo End Point 546 nm Jendrassik & Groff Method. Sulphanilic acid=5 mmol / L. Sufficient Nitrite Reagent. Two Point Calibrator within Kit. Onboard Stability of Working Reagents = 21 days. Linearity =25 mg/dL Sensitivity = 0.05 mg.% CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry date & stability.
134Serum Total Bilirubin Estimation kit for Fully Automated Biochemistry Analyzer (Single reagent) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Total bilirubin estimation kit compatible with Fully Automated Biochemistry Analyzer MIURA 2. Single reagent procedure 3. Reagent should be stabilized liquid form for ready to use. 4. Linearity: at least up to 15 mg/dL 5. Reagent stability: stable either at 2-8°C or at room temperature till date of expiry. Working reagent stable at least for 1 day. 6. Incubation time: not more than 10 minutes
135Serum Direct Bilirubin Estimation kit for Fully Automated Biochemistry Analyzer (Single reagent) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Direct bilirubin estimation kit compatible with Fully Automated Biochemistry Analyzer MIURA 2. Single reagent procedure 3. Reagent should be stabilized liquid form for ready to use. 4. Linearity: at least up to 15 mg/dL 5. Reagent stability: stable either at 2-8°C or at room temperature till date of expiry. Working reagent stable at least for 1 day. 6. Incubation time: not more than 10 minutes
136Serum ALP (Alkaline Phosphatase) Estimation Kit, AMP ( 2-Amino 2-Methyl 1-Propanol ) Buffer, Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. R1 & R2, Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 1-Nitrophenylphosphate = 15 mmol / L Linearity > 700 U/L. Sensitivity = 5 U/L %CV = 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers.long expiry date & stability.
137Serum ALP (Alkaline Phosphatase) Estimation Kit, DEA ( Diethanolamine ) Buffer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. R1 & R2, Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 1-Nitrophenylphosphate = 15 mmol / L Linearity > 700 U/L. Sensitivity = 5 U/L %CV = 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers. long expiry date & stability.
138Serum SGOT Estimation Kit Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use, Single Reagent. Enzymatic - UV Kinetic 340 nm Method. ( IFCC ) Incubation : Only 1 Minute. w/o PLP. MDH>600 U/L , NADH>0.18mmol/L Linearity 5-600 U/L Sensitivity =5 IU/L. %CV= 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers Long Expiry & Stability.
139Serum SGPT Estimation Kit Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagent. Enzymatic-UV Kinetic 340 nm Method.( IFCC). Linearity 5-400 U/L LDH>1200 U/L, NADH = 0.18mmol/L %CV= 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry & stability.
140Serum CK-MB Estimation Kit Based on IFCC Kinetic Method (Immunoinhibition) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Stable Liquid or Lypholysed Reagent reconstitution stability 30 days at 2 - 8*C Immuno inhibition UV Kinetic Method. Linearity = 1500 U/L Required CK-MB Controls Level-1 & 2 must be given with Kit. Compatible with Miura AutoAnalyser & Semi Auto analyzers .
141Serum Total CK Estimation Kit Based on IFCC UV Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents R1 & R2. Enzymatic - Kinetic 340 nm, IFCC Method. Linearity = 1500 U/L Compatible with Miura AutoAnalyser & Semi Auto analyzers Long Expiry date & stability.
142Serum LDH Estimation Kit Based on IFCC KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use R1 & R2 Reagents. UV - Kinetic 340 nm Modified Wacker Method. Linearity : 1000 U/L Compatible with Miura Fully Auto + Semi Auto Analyser. Long expiry date & stability.
143Serum GGT Estimation Kit Based on IFCC Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. R1 & R2, Enzymatic-Kinetic 405 nm Method.Glycylglycine > 100 mmol / L Linearity upto 1000 U / L. Compatible with Miura Fully Automated Analysers. Long expiry date & stability.
144Serum HDL Precipitation reagent based on Polyethylene Glycol (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagent should be stabilized liquid form 2. Should be stable at room temperature till the date of expiry 3. Sample : Precipitating reagent ratio should be 1:1 4. To be supplied with HDL cholesterol standard: 40 or 50 mg/dL or calibrator 5 mL standard to be provided per 50 mL of reagent. 5. Linearity not less than 150 mg/dL.HDL Calibrator must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers
145Serum HDL Estimation Kit Direct Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagents should be stabilized liquid form ready to use 2. To be supplied with HDL cholesterol calibrator 3. Linearity not less than 150 mg/dL.HDL Calibrator must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers
146Serum LDL Estimation Kit Direct Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use R1 & R2 Reagents.Direct Enzymatic 600 nm. Colorimetric Method. Incubation : Only 5 Minutes. Linearity = 400mg/dL Calibrator for LDL must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers.
147Serum TRIGLYCERIDE Estimation Kit based on GPO-PAP Enzymatic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagents. Enzymatic-End Point 505nm, 37"C Method. Incubation : Only 5 Min. LP.Lipase>2000U/L, POD>500U/L TG Calibrator : 200 or 300 mg/dL must be given with kit. Linearity :1000 mg/dL Compatible with Miura Fully Auto + SemiAuto Analysers.
148Serum TOTAL CALCIUM Estimation Kit based on Arsenazo III Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready Use Single Reagent. Arsenazo III Colorimetric 650 nm Endpoint Method. Incubation : Only 1 Min. Arsenazo III > 0.12 mmol / L. Linearity = 15 mg/dL Standard : 10 mg / dL. Sensitivity 0.4 mg/dL.%CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers, reagents should be in 1 ml single test vial
149CALCIUM - OCPC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. OCPC Colorimetric 570 nm Endpoint Method. Linearity = 15 mg/dL Sensitivity = 0.2mg/dL CV < 2 % Standard : 8.0mg /d L. Compatible with Miura Fully Auto + Semi Auto Analysers. About 500 - 1000 ml. Packs.
150Serum PHOSPHORUS Estimation Kit based on Phospho-Molybdate UV End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use single Reagent. UV End Point 340 nm Method. Standard : 5 mg% , Linearity : 15 mg/dL Sensitivity = 1 mg/dL. Compatible with Miura Fully Auto + Semi Auto Analysers. Long expiry date & stability.
151Serum CHLORIDE Estimation Kit based on Mercuric Thiocyanate Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagent should be stabilized liquid form 2. To be supplied with chloride standard: 100 mEq/L 3. Linearity not less than 150 mEq/L
152Serum MAGNESIUM Estimation Kit based on Xylidyl Blue Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagent. Colorimetric 570 nm End Point Method. Calmagite / Arsenazo I Standard : 2 mg/dL Calibrated. Linearity : 5 mg/dL Compatible with Miura Fully Auto + Semi Auto Analysers.
153Serum BICARBONATE Estimation Kit based on Colorimetric UV End Point/Fixed Time Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagent should be stabilized liquid form or lyophilized powder with buffer for reconstitution provided 2. Reconstituted working reagent stability: at least 1 week at 2-8 degree C 3. Provided with bicarbonate standard of 20 or 25 mmol/L 4. Linearity not less than 50 mmol/L
154Serum ALPHA(a) AMYLASE Estimation Kit based on Enzymatic Kinetic (IFCC) Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagent. Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 37" C EPS / CNPG3 Substrate Linearity = 2000 U/L. Compatible with Miura AutoAnalyser & Semi Auto analyzers. long expiry date & stability
155Serum LIPASE Estimation Kit based on Enzymatic Kinetic (IFCC) Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Lypholysed Stable Reagents. 550 nm Enzymatic -Colorimetric Method. Incubation : 10 Min. Substrate+ Activator + Buffer & Calibrator in Kit. Working reagent to have reconstituted Stability : 21 days. Linearity = 600 U/L Calibrator must be given with kit.Compatible with Miura Fully Auto + Semi Auto Analysers.
156Serum Uric Acid estimation Kit based on Uricase-POD End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. Enzymatic End Point 500 nm Method. Incubation : 5 Minutes. Uricase> 200 U/L, Standard : 6 mg%, Linearity :20 mg% Sensitivity = 0.1 mg/dL. %CV=2. Compatible with Miura Fully Auto + Semi Auto Analysers.
157Micro protein estimation Kit for determination of protein in urine & CSF based on Pyrogallol Red End-point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagent should be stabilized liquid form, ready to use. 2. To be supplied with standard of microprotein or calibrator. 3. Linearity at least 1000 mg/dL 4. Incubation up to 10 min maximum.5. Endpoint colour stability: at least 60 minutes.
158Serum Fructosamine estimation kit based on NBT Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Stable Lypholysed Reagents with buffer IFCC Kinetic 550 nm Method. Incubation : 5 Min. Working Reagent Onboard Stability = 30 days. Proteinase-K & Ketoamine Oxidase. Linearity upto 10 mMol/L 1 x 2 mL Liquid Calibrator & 2 x 1 mL Liquid Controls having open bottle stability of 30 days must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs.
159Serum Total Iron estimation kit based on Ferrozine Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagents are liquid stable ready to use or powder or tablets with buffer for reconstitution provided 2. Stability of the reconstituted reagent at least 4 weeks at 2 to 8 degree C. 1 or 2 mL reconstitution possible at a time. 3. Provided with iron standard of 1mg/L (100µg/dL) 5mL standard to be provided every 20 mL of reagent 4. Linearity not less than 800 µg/dL
160Serum Copper estimation kit based on Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Colorimetric End Point Method. Reagents : 3,5,Di Br PAESA , Ascorbic acid and Calibrated. Standard of 100 microgram / dL Incubation : 5 Minutes. Linearity : 500 microgram/dL. Compatible with Miura Fully Auto + Semi Auto Analysers.
161HDL-LDL Cholesterol Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Lyophilized calibrator for HDL and LDL cholesterol 2. Reconstitution stability of at least 1 week at 2 to 8 degree C and at least 4 weeks at -20 degree C
162CK-MB Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Lyophilized calibrator for CK-MB 2. Reconstitution stability of at least 1 week at 2 to 8 degree C 3. Provided with method specific values
163CK-MB Control Set (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Set of quality control sera of two different levels for CK-MB 2. Reconstitution stability of at least 1 week at 2 to 8 degree °C 3. Provided with method specific values.
164Bilirubin Standard (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Aqueous bilirubin standard based on human/bovine serum for total and direct bilirubin assay standardization 2. Stable for at least 1 week after opening the bottles at 2 to 8 degree C when stored in dark
165Bilirubin Standards Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Kit containing 3 to 5 levels of total and direct bilirubin standards intended for calibration verification, method evaluation and linearity check 2. Stable for at least 1 week after opening the bottles at 2 to 8 degree C when stored in dark. Kit containing 2 x 5 levels x 5 ml Combined Reference Material for Total Bilirubin and Direct Bilirubin to eneble Calibration, Linearity Checks, Method evaluation & Recovery studies. Adaptable to Miura Fully Autoanalyzer & Semi-Autoanalyzer.
166Chemistry Standards Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Kit containing 3 to 5 levels of combined reference material for glucose, urea, creatinine, triglycerides, potassium, sodium & chloride in aqueous matrix for calibration verification, method evaluation and linearity check 2. Stable for at least 6 months after opening the bottles when stored as per manufacturer’s instructions
167Blood Gas Controls – Pack of Normal and Abnormal level (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Multilevel Multianalyte blood gas controls containing pO2, pCO2, pH, sodium, potassium, ionized calcium 2. Stable till expiry at 2 to 8 degree C 3. Provided with method and instrument specific values
168Blood Gas Controls –Abnormal level (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Multianalyte blood gas controls containing pO2, pCO2, pH, sodium, potassium, ionized calcium 2. Stable till expiry at 2 to 8 degree C 3. Provided with method and instrument specific values
169Fructosamine Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Lyophilized calibrator for fructosamine 2. Reconstitution stability of at least 1 week at 2 to 8 degree C 3. Provided with method specific values
170Sampling Precision Test Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Kit for checking proper functioning of the sample fluid metering and photometric measuring system 2. Provided with detailed literature and/or software for calculation of sampling precision
171Reagent Precision Test Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Kit for checking proper functioning of the reagent fluid metering and photometric measuring system 2. Provided with detailed literature and/or software for calculation of reagent precision
172Quality Control Serum (Normal Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature )1. The product must be multi-analyte normal level quality control serum prepared from pooled human sera and intended for verification of precision of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters and hormones i.e. Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests.
173Quality Control Serum (Pathological- Higher level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature )1. The product must be multi-analyte pathological (high level) quality control serum prepared from pooled human sera and intended for verification of precision and accuracy of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters and hormones i.e. Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH. 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached.8. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests.
174Quality Control Serum (Pathological- Lower level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature )1. The product must be multi-analyte lower level quality control serum prepared from pooled human sera and intended for verification of precision and accuracy of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters. 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 8. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests.
175Multicalibrator Sera for Clinical Chemistry Assays (Normal Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature)1. The product must be Normal level multicalibration serum intended for calibration of clinical chemistry assays suitable for automated analyzers and manual procedures. Calibrator sera should contain all routinely measured parameters. It must contain the following parameters: Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 2. The calibrator must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 3. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 4. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 5. Company should have ISO certificate. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 6. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests.
176Multicalibrator Sera for Clinical Chemistry Assays (Higher Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature)1. The product must be Higher Level multicalibration serum intended for calibration of clinical chemistry assays suitable for automated analyzers and manual procedures.Calibrator sera should contain all routinely measured parameters. It must contain the following parameters: Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 2. The calibrator must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 3. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 4. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 5. Company should have ISO certificate. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 6. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests.
177Multi-parameter External Quality Assessment Scheme for Routine Clinical Chemistry Investigations (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature)1.It should a well recognized scheme having large number of participants and effective consolidated programme having once monthly or once biweekly sample frequency. 2. The samples provided should be lyophilized human serum samples.3. The analyte values in the sample should cover clinically relevant ranges to test accuracy and precision of the reported results. 4.The scheme must deliver regular reports in user friendly format with rapid turnaround. 5. The results must include reference method results as well as results for instruments and methods used by participating laboratory and other routine methods. 6. The results should help identify trends, biases and precision problems using appropriate statistical data and graphs. 7. The participating laboratory should have access to advisory panel to troubleshoot any technical queries and to get advice regarding corrective actions. 8. The scheme must provide certificate of participation at the end of the cycle. 9. The EQA scheme system must be ISO/IEC certified
178AMMONIA ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable / Lypholysed Reagents. UV - End Point Method. NADPH > 0.25mmol/L GLDH>1000U/L. Standard: 0.5 mg% Linearity : 2 mg% Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs
179C - Reactive Protein Calibrator Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid ready use calibrator having 30 days open bottle stability when stored at 2-8*C, Adaptable to MiuraFully Autoanalyzer. 5 x 2 mL packs
180C - Reactive Protein Control Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing liquid control solutions Level-1 and Level -2 for High sensitivity CRP Immunoturbidimetric Estimation Kit. Open bottle atability of 30 days at 2 - 8*C.Adaptable to Miura Autoanalyzer.2 x 3 mL packs
181CHOLINESTERASE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Enzymatic - Kinetic Method. DTNB , Butyryl thiocholine substrate Linearity > 6000 U / L Compatible with MiuraFully Auto + Semi Auto Analyser. About 50 ml. Packs.
182G6 PDH ESTIMATION KIT (QUANTITATIVE) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable R1, R2, R3 Ready use Reagents. Enzymatic Kinetic 340 nm Method. Incubation : Only 5 Minutes. Cholesterol Oxidase > 180 U / L Compatible with Miura Fully Auto + SemiAuto Analyser. About 50 - 100 Test Packs.
183Immunoturbidi metric Kit for HbA1C (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing Ready use, liquid stable reagents R1, R2 & R3 having linearity upto 15 gm %, Immunoturbidimetric 660 nm photometric method. Adaptable on Miura FullyAuto analyzer & semi auto analyzer, with controls level 1 and 2, calibrator
184HbA1C Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Lyophilised calibrators having reconstitution stability of minimum 30 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 4 x 0.5 mL packs.
185HbA1C Control Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Set of Controls Level 1 & Level 2 having reconstitution stability of minimum 30 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 2 x 0.5 mL packs
186Hemolysis Reagent for Immunoturbidi metric HbA1C Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing Ready use, liquid stable reagent for Total HbA1C Immunoturbidimetric estimation.
187Homocysteine Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid ready use calibrators having long stability when stored at 2-8*C, Adaptable to Semi-Auto & Miura Fully Autoanalyzer. 2 x 2 x 3 mL packs
188HOMOCYSTEINE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Reagents. R1, R2, R3. Enzymatic UV Kinetic 340 nm Method. Calibrators must be supplied with Kit having reconsituted open bottle stability of 30 days.Linearity 50 umol / L. Compatible with MiuraFully Auto + Semi Auto Analysers. 50 - 100 mL Packs.
189IgA. Immunoglobulin A ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable / Lypholysed Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgA antibody (human) Calibrator/ Controls with kit. Compatible with Miura Fully Automated Analyser. About 50 ml. Packs.
190IgG. Immunoglobulin G ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable / Lyophilised Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgG antibody (human) Calibrator / Controls with kit. Compatible with Miura Fully Automated Analysers. About 50 ml. Packs.
191IgM. Immunoglobulin M ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable / Lyophilysed Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgM antibody (human) Calibrator or Controls with kit. Compatible with Miura Fully Automated Analysers. About 50 ml. Packs.
192Immunoturbidi metric Kit for C -Reactive Protein (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing liquid stable reagents R1 & R2 having linearity of 0.1 - 300 mg / dL High sensitivity CRP Antibody / Latex Turbidity, 570 nm photometric method. Adaptable on Miura FullyAutoanalyzer
193Immunoturbidi metric Kit for Microalbumin (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing liquid stable reagents R1 & R2 having linearity of 0.5 - 30 mg / dL, 340 / 700 nm photometric method. Adaptable on Miura FullyAutoanalyzer
194Immunoturbidi metric Kit for Pre Albumin (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing ready use liquid stable reagents R1 & R2 having linearity upto 60 mg / dL, Immunoturbidimetric 340 / 700 nm photometric method. Adaptable on Miura Fully Autoanalyzer
195IRON ( TOTAL ) ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. 630 nm Chromazurol - End Point Method. Incubation : Only 5 Min. Chromazurol : 2 mmol/L Standard : 1mg/L , Linearity : 5 mg/L Compatible with Miura Fully Auto + Semi Auto Analysers. About 200 - 500 ml. Packs.
196LACTATE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Enzymatic - End Point Method. Incubation : Only 5 Minutes. Peroxidase>1800 U/L , Standard : 40 mg/dL Linearity : 100 mg / dL. Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs.
197MICRO-ALBUMIN ( Micro-Protein ) IN CSF / SERUM / URINE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready use Single Reagents. Colorimetric End Point 600 nm Method. Pyrogallol red : 0.06 mmol / L Standard : 50 mg % Sensitivity 10 mg/dL. %CV=1.5 Calibrator & Controls Level 1& 2 having 6 months open bottle stability with Kit. Linearity : 200 mg % Compatible with Miura Fully Auto + Semi Auto Analysers. About 500 ml. Packs.
198Micro-Albumin Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid ready use Liquid calibrators having stability of minimum 30 days at 2 - 8*C Adaptable to Miura Fully Autoanalyzer. 6 x 1 mL packs
199Micro-Albumin Controls Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid ready use Liquid calibrators having stability of minimum 30 days at 2 - 8*C Adaptable to Miura Fully Autoanalyzer. 6 x 1 mL packs
200PANCREATIC ALPHA AMYLASE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Antibody-Enzymatic Kinetic Method. Incubation : Only 5 Min. Substrate : Ethylidene G7pNP Glucosidase >20 U/L Linearity : 1500 U/L. Compatible with Miura Fully Auto + Semi Auto Analysers. 100 mL Packs
201Serum Cystatin -C Estimation Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagent Kit. Photometric Assay. Adaptable to Miura Autoanalyzer. Shelf life = 1 year and on board stability of opened reagent should be atleast 14 days. Kit must contain Calibrators & QC material
202HbA1c Estimation kit for Fully Automated Biochemistry Analyzer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagents are liquid stable ready to use 2. Provided with HbA1c calibrator 3. Sensitivity: 0.3 gm/dL or better 4. Linearity: 2.5 gm/dL or better (or up to 15%)
203HbA1c estimation kit based on affinity chromatography Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. Reagents are liquid stable ready to use or powder or tablets with buffer for reconstitution provided 2. Provided with HbA1c calibrator 3. Detection range: 3% to 15% or wider
204Serum Ferritin kit (Latex Turbidimetry Method) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1x40 ml R1 Diluent, 1x10 ml R2 Latex, 1x3 ml FERR-CAL
205Total Iron Standard Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Kit containing 5 x 15 ml Combined Reference Material for Total Iron & Ammonia to eneble Calibration, Linearity Checks, Method evaluation & Recovery studies. Adaptable to Miura Fully Autoanalyzer.
206UIBC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Ready Use Reagents. Ferrozine EndPoint 560 nm method. Linearity upto 500 ugm/dL Adaptable to Miura Autoanalyzer & Semi-Auto analysers. 200 - 500 mL packs.
207ZINC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Liquid Stable Reagents. Colorimetric Method. Chelation with 5-Br-PAPS. Standard of 200 micrograms. Linearity : 1000 micrograms. Incubation : 5 Min. Compatible with MiuraFully Auto + semi Auto Analysers. About 100 mL Packs
208HDL / LDL Cholesterol Control Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Lyophilised combined reagent having reconstitution stability of minimum 7 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 10 x 3 mL packs
209Rapid Troponin-I Card Test (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. One step rapid chromatographic immunoassay for detection of troponin-I in whole blood or serum 2. Read time not more than 15 minutes 3. Sensitivity 1ng/mL or better 4. Sample volume required 200µL or less 5. Each cassette provided with dropper 6. Stable at room temperature till expiry
210Cassette for detection of Acute Myocardial Infarction (Troponin-I, CK-MB and Myoglobin) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. One step rapid chromatographic immunoassay for detection of troponin-I, CK-MB and Myoglobin in whole blood or serum 2. Read time not more than 15 minutes 3. Sensitivity: Troponin-I : 1ng/mL or better CK-MB : 5 ng/mL or better Myoglobin : 100 ng/mL or better 4. Sample volume required 300µL or less 5. Each cassette provided with dropper 6. Stable at room temperature till expiry
211Serum T3 (Triiodothyronine) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. ELISA kit for quantitative determination of T3 in human serum containing 96 well antibody coated microtitre plate, ready to use T3 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.1 ng/mL or lower 4. Opened kit stable till expiry date when stored as per manufacture instructionsEnclose all details of Composition, CV & Precision data of Kit.
212Serum Free T3 (Free Triiodothyronine) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )1. ELISA kit for quantitative determination of T3 in human serum containing 96 well antibody coated microtitre plate, ready to use T3 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.07 pg/mL or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit.
213Serum T4 (Thyroxin) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of T4 in human serum containing 96 well antibody coated microtitre plate, ready to use T4 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 10 nmol/L or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit.
214Serum Free T4 (Free Thyroxin) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of T4 in human serum containing 96 well antibody coated microtitre plate, ready to use T4 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.08 ng/dL or lower
215Serum TSH (Thyroid Stimulating Hormone) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer. ELISA kit for quantitative determination of TSH in human serum containing 96 well antibody coated microtitre plate, ready to use TSH reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.1 mIU/mL or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit.
216Preventive maintenance (PM) kit for Erba CHEM 5 Plus V2 semiauto-analyzer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Preventive maintenance (PM) kit for Transasia Erba CHEM 5 Plus V2 semiauto-analyzer
217Serum Anti-TPO Antibodies Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ).Streptavidin Biotin Based Sandwich Assay 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
218Serum CA-19.9 Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
219Serum Alpha Feto Protein Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
220Serum beta-HCG Estimation Elisa kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
221Serum PSA Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
222Serum CEA Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
223Serum FSH Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
224Serum LH Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
225MULTI ASSAY HUMAN SERA BASED TUMOUR MARKER CONTROLS KIT FOR LABORATORY Q.C. (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer. LEVEL I & II (Normal & pathological)
226Serum CA-125 Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of CA 125 in human serum containing 96 well antibody coated microtitre plate, ready to use CA 125 reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure
227Serum Adiponectin Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of adiponectin in human serum containing 96 well antibody coated microtitre plate, ready to use adiponectin reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure . sensitivity of < 25 pg/ml. sample volume less than 100 µL
228Serum Leptin Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of leptin in human serum containing 96 well antibody coated microtitre plate, ready to use leptin reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure . sensitivity of < 3.5 pg/ml. sample volume less than 100 µL
229Serum CA-15.3 Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer )Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests.
230Bees waxAs per Column no.2
231TLE 1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
232PDL 1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
233PAX 5Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
234DOG-1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
235STAT6Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
236NUTAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
237MUC 1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
238MUC5ACAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
239MUC6Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
240MUC4Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
241TFE3BAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
242B72.3Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
243BCL10Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
244BCL6 OncoproteinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
245Beta-AmyloidAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
246BG-8Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
247CA19-9Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
248Cathepsin BAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
249CD3Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
250CD103Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
251Cd11cAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
252CD123Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
253CD13Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
254CD138Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
255CD14Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
256CD19Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
257CD1aAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
258CD2Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
259CD22Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
260CD23Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
261CD24Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
262CD25Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
263CD33Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
264CD36Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
265CD38Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
266CD3-epsilon chainAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
267CD4Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
268CD43Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
269CD45Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
270CD45RAAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
271CD45ROAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
272CD61Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
273CD64Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
274CD7Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
275CD71Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
276CD9Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
277Collagen IVAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
278Cytokerain18Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
279D2-40Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
280EBERAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
281EBVAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
282EGFRAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
283Epstein barr virus early antigenAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
284Epstein-Barr Virus(LMP)Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
285F13aAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
286F8Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
287FL1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
288GHAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
289GlucagonAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
290Glycophorin AAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
291Growth hormoneAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
292HBME-1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
293HbsAgAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
294Hemoglobin AAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
295HIV,p24Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
296HLADRAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
297IgA,Specific for Alpha-ChainsAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
298IgG,Specific for gamma chainsAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
299IgM,specific for Mu-chainsAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
300IMP3Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
301INI 1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
302InsulinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
303J chainAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
304Kappa light chainsAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
305Lambda light chainsAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
306MammaglobinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
307Mast cell tryptaseAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
308MITFAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
309MOC-31Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
310MUC2 ProteinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
311MUM1 ProteinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
312Myelin Basic ProteinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
313MyoD1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
314NapsinAAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
315NESTINAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
316OCT--4Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
317PAP(Prostatic acid phosphatase)Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
318P 16Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
319PCNAAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
320PE-10Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
321Plasma cell (Clone Vs38c)Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
322PPAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
323PRAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
324PTENAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
325PTHAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
326RCCAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
327S-100Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
328SomatostatinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
329TIA-1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
330TRAPAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
331TryptaseAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
332NKX3.1Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
333EZ-Dewax solutionAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
334Alpha - 1 - AntitrypsinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
335Alpha - 1 - AntichymotrypsinAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
336CD 13Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
337CD 14Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
338CD 16Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
339CDw 75Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
340CK 5Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
341CK8 & 18Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
342CK 14Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
343CK 15Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
344CK 16Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
345CK 17Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
346CK 18Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
347WT 1(Antibody to carboxy terminal)Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
348EpcamAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
349Factor VIII related antigenAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
350Factor XIII AAntibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
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We takes all possible care for accurate & authentic tender information, however Users are requested to refer Original source of Tender Notice / Tender Document published by Tender Issuing Agency before taking any call regarding this tender.
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