Pure Global

Luteinizing Hormone Rapid Test - India CDSCO Medical Device Registration

Luteinizing Hormone Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_c55378125c7d56372c606041ffdf9efb_e78652c07bc282cd6170f57c89aaa8b0. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi 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
Luteinizing Hormone Rapid Test
UID: MFG/IVD/2023/000113_c55378125c7d56372c606041ffdf9efb_e78652c07bc282cd6170f57c89aaa8b0

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

The Chimeraยฎ LH Test is a rapid immuno-chromatographic assay for the qualitative detection of luteinizing hormone (Chimera) in urine. This test is for in vitro screening used in obtaining a visual qualitative result for LH in urine to predict the time of ovulation.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing