Pure Global

Progesterone Rapid Quantitative Test - India CDSCO Medical Device Registration

Progesterone Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_203188dffbe6267a4155300069b7ac90_b438f9a42a56b149c9929c08e3763a7c. The license holder is RAPID DIAGNOSTIC 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 Rapid Quantitative Test
UID: IMP/IVD/2020/000278_203188dffbe6267a4155300069b7ac90_b438f9a42a56b149c9929c08e3763a7c

Device Class

Class B

Approving Authority

CDSCO

Product Information

Intended for quantitative determination of Progesterone in human serum, whole blood or plasma. The test is used as an aid to the track ovulation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing