Pure Global

Progesterone Test - India CDSCO Medical Device Registration

Progesterone Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_943d0ff03a9779731dea9beb14c62011_e0bafbc4043841b6ca4d2806ecf2d979. This device is marketed under the brand name Finecare Beta-HCG Rapid Quantitative Test. The license holder is Star Biomed Pvt. Ltd., and it is classified as Device Class Class B. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Progesterone Test
UID: IMP/IVD/2021/000413_943d0ff03a9779731dea9beb14c62011_e0bafbc4043841b6ca4d2806ecf2d979

Brand Name

Finecare Beta-HCG Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FinecareTM Progesterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecareโ„ข FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative determination of progesterone in human serum, plasma or whole blood

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing