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

TDR : 38614137

Tender Notice
Corrigendum Details
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Vadodara , Gujarat

Tender Brief : 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

Document Fees
₹ 5000 /-

EMD
₹ 200000.0 /-

Tender Value
Refer document

Submission Date
17-08-2023

Competition Type
Indian

Bidding Type
Tender

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Sr No	Corrigendum Date	Corrigendum	Type	New Submission Date
1	31-07-2023			17-08-2023

Sl. No.	Item Title	Specification
1	Pro-Clacitonin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
2	ferritin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
3	D-dimer	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
4	Vitamin B12	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
5	Vitamin B3	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
6	Troponin I & T (Quanitative)	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
7	Beta HCG	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
8	Beta 2 microglobulin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
9	Alpha 1 Antitrypsin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
10	Apo-Lipoprotein A1 & B	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
11	Ceruloplasmin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
12	Heptoglobin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
13	BNP	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
14	Lipoprotein A	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
15	Insulin	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
16	PTH	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
17	Vitamin D	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
18	Zinc	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
19	Ammonia	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
20	Total Iron	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
21	hs-CRP	Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430
22	Pro-Clacitonin	Automated Chemileuminisecence based Immunoassay test
23	IL-6	Automated Chemileuminisecence based Immunoassay test
24	D-dimer	Automated Chemileuminisecence based Immunoassay test
25	Vitamin B12	Automated Chemileuminisecence based Immunoassay test
26	Vitamin B3	Automated Chemileuminisecence based Immunoassay test
27	Troponin I & T (Quanitative)	Automated Chemileuminisecence based Immunoassay test
28	Beta HCG	Automated Chemileuminisecence based Immunoassay test
29	Beta 2 microglobulin	Automated Chemileuminisecence based Immunoassay test
30	Alpha 1 Antitrypsin	Automated Chemileuminisecence based Immunoassay test
31	Apo-Lipoprotein A1	Automated Chemileuminisecence based Immunoassay test
32	Apo-Lipoprotein B	Automated Chemileuminisecence based Immunoassay test
33	Ceruloplasmin	Automated Chemileuminisecence based Immunoassay test
34	Heptoglobin	Automated Chemileuminisecence based Immunoassay test
35	Lipoprotein A	Automated Chemileuminisecence based Immunoassay test
36	Transferrin	Automated Chemileuminisecence based Immunoassay test
37	Galactin-3	Automated Chemileuminisecence based Immunoassay test
38	Estradiol	Automated Chemileuminisecence based Immunoassay test
39	Progesterone	Automated Chemileuminisecence based Immunoassay test
40	Prolactin	Automated Chemileuminisecence based Immunoassay test
41	AMH	Automated Chemileuminisecence based Immunoassay test
42	Testosterone	Automated Chemileuminisecence based Immunoassay test
43	C-Peptide	Automated Chemileuminisecence based Immunoassay test
44	Cortisol	Automated Chemileuminisecence based Immunoassay test
45	Insulin	Automated Chemileuminisecence based Immunoassay test
46	PTH	Automated Chemileuminisecence based Immunoassay test
47	Vitamin D3	Automated Chemileuminisecence based Immunoassay test
48	TSH	Automated Chemileuminisecence based Immunoassay test
49	Free T4	Automated Chemileuminisecence based Immunoassay test
50	Free T4	Automated Chemileuminisecence based Immunoassay test
51	Anti- TPO	Automated Chemileuminisecence based Immunoassay test
52	Lactate	Automated Chemileuminisecence based Immunoassay test
53	Fructosamine	Automated Chemileuminisecence based Immunoassay test
54	UIBC	Automated Chemileuminisecence based Immunoassay test
55	TIBC	Automated Chemileuminisecence based Immunoassay test
56	PSA (Total)	Automated Chemileuminisecence based Immunoassay test
57	PSA (Free)	Automated Chemileuminisecence based Immunoassay test
58	FSH	Automated Chemileuminisecence based Immunoassay test
59	LH	Automated Chemileuminisecence based Immunoassay test
60	Leptin	Automated Chemileuminisecence based Immunoassay test
61	Adiponectine	Automated Chemileuminisecence based Immunoassay test
62	Zinc	Automated Chemileuminisecence based Immunoassay test
63	Inhibin	Automated Chemileuminisecence based Immunoassay test
64	CA 27.29	Automated Chemileuminisecence based Immunoassay test
65	CA 15.3	Automated Chemileuminisecence based Immunoassay test
66	CA 19-9	Automated Chemileuminisecence based Immunoassay test
67	CEA	Automated Chemileuminisecence based Immunoassay test
68	Ca 125	Automated Chemileuminisecence based Immunoassay test
69	AFP	Automated Chemileuminisecence based Immunoassay test
70	Cystatin C	Automated Chemileuminisecence based Immunoassay test
71	BNP	Compatible with ELISA Reader and Washer.
72	Transferrin	Compatible with ELISA Reader and Washer.
73	Galactin-3	Compatible with ELISA Reader and Washer.
74	Estradiol	Compatible with ELISA Reader and Washer.
75	Progesterone	Compatible with ELISA Reader and Washer.
76	Prolactin	Compatible with ELISA Reader and Washer.
77	AMH	Compatible with ELISA Reader and Washer.
78	Testosterone	Compatible with ELISA Reader and Washer.
79	C-Peptide	Compatible with ELISA Reader and Washer.
80	Cortisol	Compatible with ELISA Reader and Washer.
81	Insulin	Compatible with ELISA Reader and Washer.
82	PTH	Compatible with ELISA Reader and Washer.
83	Vitamin D	Compatible with ELISA Reader and Washer.
84	Free T3	Compatible with ELISA Reader and Washer.
85	Free T4	Compatible with ELISA Reader and Washer.
86	Lactate	Compatible with ELISA Reader and Washer.
87	Fructosamine	Compatible with ELISA Reader and Washer.
88	UIBC	Compatible with ELISA Reader and Washer.
89	TIBC	Compatible with ELISA Reader and Washer.
90	PSA (Total &Free)	Compatible with ELISA Reader and Washer.
91	FSH	Compatible with ELISA Reader and Washer.
92	LH	Compatible with ELISA Reader and Washer.
93	Leptin	Compatible with ELISA Reader and Washer.
94	Adiponectine	Compatible with ELISA Reader and Washer.
95	Zinc	Compatible with ELISA Reader and Washer.
96	Ammonia	Compatible with ELISA Reader and Washer.
97	Measuring Cartridge	Compatible with ABG analyzer RAPID Point 500e
98	Wash Cartridge	Compatible with ABG analyzer RAPID Point 500e
99	Sample Cup	Compatible with Fully Automated analyzer Erba XL- 640/ Mindray Bs-430
100	Auto wash	Compatible with Fully Automated Analyzer Erba Xl-640
101	Acid -Alkaline Wash	Compatible with Fully Automated Analyzer Erba Xl-640
102	Cuvette	Compatible with Fully Automated analyzer Erba XL- 640
103	Cuvette	Compatible with Fully Automated analyzer Mindray Bs-430
104	Reagent Bottle	20 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400
105	Reagent Bottle	40 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400
106	Reagent Bottle	20 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430
107	Reagent Bottle	40 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430
108	CD-8 Wash Solution	Compatible with Fully Automated Analyzer Mindray BS-430
109	Electrolyte Reagent Pack	Compatible with Acculyte 3P Electrolyte Analyzer
110	Deproteinizer	Compatible with Acculyte 3P Electrolyte Analyzer
111	Heparinized Glass capillaries for Bill-P Bilirubinometer	Compatible with Bill-P Bilirubinometer
112	Serum Iron estimation kit*	Based on Ferrozine Colorimetric End Point Method, R1 & R2 reagent, liquid reagent,linearity 1000 µg/dI
113	Serum Ferritin estimation kit*	Based on Immunoturbidimetric method, R1 & R2 reagent,liquid reagent, linearity 600 µg/dI
114	Hankâ€™s Balanced Salt Solution 10 XWith Phenol red without Sodium bicarbonate	As per Column no.2
115	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	As per Column no.2
116	Hb-sensor unit	Original
117	Hb-sensor casing	Original
118	Photo-electric sensor device(LS)	Original
119	device for specimen input (DS)	Original
120	Waste bottle sensor device with cable	Original
121	Plasma GLUCOSE Estimation kit based on GOD-POD ENZYMATIC End â€“ 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.
122	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 )	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.
123	Serum 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.
124	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 )	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.
125	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 )	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.
126	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 )	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.
127	Serum TOTAL CHOLESTEROL Estimation kit based on CHOD-POD ENZYMATIC End â€“ 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.
128	Serum CREATININE Estimation Kit based on Jaffeâ€™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.
129	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 )	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.
130	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 )	Liquid Stable Ready Use Single Reagent. Biuret - End Point 540 nm Method. Linearity: 15 Gm / dL Compatible with Miura Fully Auto + Semi Auto Analysers.
131	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 )	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.
132	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 )	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.
133	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 )	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.
134	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 )	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
135	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 )	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
136	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 )	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.
137	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 )	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.
138	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 )	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.
139	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 )	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.
140	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 )	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 .
141	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 )	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.
142	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 )	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.
143	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 )	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.
144	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 )	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
145	Serum 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
146	Serum 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.
147	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 )	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.
148	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 )	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
149	CALCIUM - 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.
150	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 )	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.
151	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 )	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
152	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 )	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.
153	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 )	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
154	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 )	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
155	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 )	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.
156	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 )	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.
157	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 )	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.
158	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 )	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.
159	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 )	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
160	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 )	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.
161	HDL-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
162	CK-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
163	CK-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.
164	Bilirubin 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
165	Bilirubin 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.
166	Chemistry 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 manufacturerâ€™s instructions
167	Blood Gas Controls â€“ 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
168	Blood Gas Controls â€“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
169	Fructosamine 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
170	Sampling 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
171	Reagent 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
172	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 )	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.
173	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 )	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 â€“ 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.
174	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 )	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 â€“ 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.
175	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)	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 â€“ 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.
176	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)	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 â€“ 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.
177	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)	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
178	AMMONIA 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
179	C - 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
180	C - 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
181	CHOLINESTERASE 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.
182	G6 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.
183	Immunoturbidi 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
184	HbA1C 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.
185	HbA1C 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
186	Hemolysis 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.
187	Homocysteine 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
188	HOMOCYSTEINE 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.
189	IgA. 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.
190	IgG. 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.
191	IgM. 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.
192	Immunoturbidi 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
193	Immunoturbidi 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
194	Immunoturbidi 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
195	IRON ( 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.
196	LACTATE 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.
197	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 )	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.
198	Micro-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
199	Micro-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
200	PANCREATIC 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
201	Serum 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
202	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 )	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%)
203	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 )	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
204	Serum 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
205	Total 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.
206	UIBC 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.
207	ZINC 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
208	HDL / 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
209	Rapid 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
210	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 )	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
211	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 )	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.
212	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 )	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.
213	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 )	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.
214	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 )	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
215	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 )	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.
216	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 )	Preventive maintenance (PM) kit for Transasia Erba CHEM 5 Plus V2 semiauto-analyzer
217	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 )	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.
218	Serum 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.
219	Serum 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.
220	Serum 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.
221	Serum 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.
222	Serum 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.
223	Serum 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.
224	Serum 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.
225	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 )	Compatible with ELISA Reader and Washer. LEVEL I & II (Normal & pathological)
226	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 )	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
227	Serum 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
228	Serum 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
229	Serum 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.
230	Bees wax	As per Column no.2
231	TLE 1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
232	PDL 1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
233	PAX 5	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
234	DOG-1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
235	STAT6	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
236	NUT	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
237	MUC 1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
238	MUC5AC	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
239	MUC6	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
240	MUC4	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
241	TFE3B	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
242	B72.3	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
243	BCL10	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
244	BCL6 Oncoprotein	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
245	Beta-Amyloid	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
246	BG-8	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
247	CA19-9	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
248	Cathepsin B	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
249	CD3	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
250	CD103	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
251	Cd11c	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
252	CD123	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
253	CD13	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
254	CD138	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
255	CD14	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
256	CD19	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
257	CD1a	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
258	CD2	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
259	CD22	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
260	CD23	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
261	CD24	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
262	CD25	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
263	CD33	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
264	CD36	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
265	CD38	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
266	CD3-epsilon chain	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
267	CD4	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
268	CD43	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
269	CD45	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
270	CD45RA	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
271	CD45RO	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
272	CD61	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
273	CD64	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
274	CD7	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
275	CD71	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
276	CD9	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
277	Collagen IV	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
278	Cytokerain18	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
279	D2-40	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
280	EBER	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
281	EBV	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
282	EGFR	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
283	Epstein barr virus early antigen	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
284	Epstein-Barr Virus(LMP)	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
285	F13a	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
286	F8	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
287	FL1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
288	GH	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
289	Glucagon	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
290	Glycophorin A	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
291	Growth hormone	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
292	HBME-1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
293	HbsAg	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
294	Hemoglobin A	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
295	HIV,p24	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
296	HLADR	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
297	IgA,Specific for Alpha-Chains	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
298	IgG,Specific for gamma chains	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
299	IgM,specific for Mu-chains	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
300	IMP3	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
301	INI 1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
302	Insulin	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
303	J chain	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
304	Kappa light chains	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
305	Lambda light chains	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
306	Mammaglobin	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
307	Mast cell tryptase	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
308	MITF	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
309	MOC-31	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
310	MUC2 Protein	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
311	MUM1 Protein	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
312	Myelin Basic Protein	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
313	MyoD1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
314	NapsinA	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
315	NESTIN	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
316	OCT--4	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
317	PAP(Prostatic acid phosphatase)	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
318	P 16	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
319	PCNA	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
320	PE-10	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
321	Plasma cell (Clone Vs38c)	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
322	PP	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
323	PR	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
324	PTEN	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
325	PTH	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
326	RCC	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
327	S-100	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
328	Somatostatin	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
329	TIA-1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
330	TRAP	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
331	Tryptase	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
332	NKX3.1	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
333	EZ-Dewax solution	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
334	Alpha - 1 - Antitrypsin	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
335	Alpha - 1 - Antichymotrypsin	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
336	CD 13	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
337	CD 14	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
338	CD 16	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
339	CDw 75	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
340	CK 5	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
341	CK8 & 18	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
342	CK 14	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
343	CK 15	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
344	CK 16	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
345	CK 17	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
346	CK 18	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
347	WT 1(Antibody to carboxy terminal)	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
348	Epcam	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
349	Factor VIII related antigen	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use
350	Factor XIII A	Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use

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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

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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

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