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Human Chronic Gonadotropin test kits - India CDSCO Medical Device Registration

Human Chronic Gonadotropin test kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_63f71aa5821a7547752021957542d29a_7ef70c7a8f11c45e39e86a02ab56f5cc. This device is marketed under the brand name hCG. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, and it is classified as Device Class Class B. The approving authority is Pune 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.

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CDSCO Registered
Class Class B
Human Chronic Gonadotropin test kits
UID: MFG/IVD/2021/000062_63f71aa5821a7547752021957542d29a_7ef70c7a8f11c45e39e86a02ab56f5cc

Brand Name

hCG

Device Class

Class B

Approving Authority

Pune Division

Product Information

Pregnancy Detection Kit is a rapid chromatographic immunoassay for the qualitative detection of human Chorionic Gonadotropin (hCG) in human urine to aid in the early detection of pregnancy. This test is an in vitro diagnostic use test and is intended for professional testing

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