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Progesterone Detection Kit - India CDSCO Medical Device Registration

Progesterone Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000498_20e29a5d08f47495023e98b5b90846ab_e050243c1eabfbdd57a4d11c861b09b1. 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
Progesterone Detection Kit
UID: IMP/IVD/2021/000498_20e29a5d08f47495023e98b5b90846ab_e050243c1eabfbdd57a4d11c861b09b1

Brand Name

Fluorescence Dry Quantitative Immunoassay

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitatively measuring the concentration of progesterone in female serum/plasma/whole-blood

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