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Neutrophil gelatinase-associated lipocalin assay kit - India CDSCO Medical Device Registration

Neutrophil gelatinase-associated lipocalin assay kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000498_89e41b3be2aa0b39b14a2e791dfe2cce_f4b98b9a12f432aff5e26b50af2a279a. This device is marketed under the brand name Fluorescence Dry Quantitative Immunoassay. The license holder is Rivaara Labs Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
Neutrophil gelatinase-associated lipocalin assay kit
UID: IMP/IVD/2021/000498_89e41b3be2aa0b39b14a2e791dfe2cce_f4b98b9a12f432aff5e26b50af2a279a

Brand Name

Fluorescence Dry Quantitative Immunoassay

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitatively measuring the concentration of neutrophil gelatinase associated lipocalin (Fluorescence Dry Quantitative Immunoassay) in human blood / plasma/ serum/ urine

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