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Human Chorionic Gonadotropin test reagents/kits - India CDSCO Medical Device Registration

Human Chorionic Gonadotropin test reagents/kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000061_cebbf3e1c495835838e836f980f5ab24_2e1a69c7ed3d8d684904c1c449e10950. This device is marketed under the brand name hCG. The license holder is SANCARA MD PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Punjab.

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 B
Human Chorionic Gonadotropin test reagents/kits
UID: MFG/IVD/2021/000061_cebbf3e1c495835838e836f980f5ab24_2e1a69c7ed3d8d684904c1c449e10950

Brand Name

hCG

Device Class

Class B

Approving Authority

Punjab

Product Information

hCG is intended for the qualitative detection of human chorionic gonadotropin (hCG) in urine as an aid in the diagnosis of pregnancy

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