Pure Global

LH ovulation Test kit - India CDSCO Medical Device Registration

LH ovulation Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000132_64fa28357710f7fb0d6ba30450d7542e_47da1625cd96b683af55209cdc176274. The license holder is Seloi Healthcare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai Division.

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
LH ovulation Test kit
UID: MFG/IVD/2022/000132_64fa28357710f7fb0d6ba30450d7542e_47da1625cd96b683af55209cdc176274

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

The LH Ovulation Rapid Test Device ##PLACEHOLDER_0## is a rapid chromatographic immunoassay for the qualitative detection of luteinizing hormone ##PLACEHOLDER_0## in urine to aid in the detection of ovulation.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing