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Lipoprotein associated phospholipase A2 Detection Kit - India CDSCO Medical Device Registration

Lipoprotein associated phospholipase A2 Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000498_1d04384ba94e55619b29b5b596c9d15d_77fe3c41b0bae87260c67de4858f170b. 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 B. The approving authority is CDSCO.

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CDSCO Registered
Class Class B
Lipoprotein associated phospholipase A2 Detection Kit
UID: IMP/IVD/2021/000498_1d04384ba94e55619b29b5b596c9d15d_77fe3c41b0bae87260c67de4858f170b

Brand Name

Fluorescence Dry Quantitative Immunoassay

Device Class

Class B

Approving Authority

CDSCO

Product Information

Quantitative determination of Lipoprotein associated phospholipase A2 (Fluorescence Dry Quantitative Immunoassay) concentration in serum, plasma and whole blood

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