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Serum amyloid A Detection Kit - India CDSCO Medical Device Registration

Serum amyloid A Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000498_389fb23299a78a6916b5c75b8bef8871_2f31c53a8ebbbdcbc1106b30ba43fef4. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Serum amyloid A Detection Kit
UID: IMP/IVD/2021/000498_389fb23299a78a6916b5c75b8bef8871_2f31c53a8ebbbdcbc1106b30ba43fef4

Brand Name

Fluorescence Dry Quantitative Immunoassay

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitative determination of Serum amyloid A (Fluorescence Dry Quantitative Immunoassay) concentration in human serum, plasma and whole blood

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