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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_8fbd963c21cad7918e2e14be9f25828c_0bcd594c05270c784251435f39c1b019. 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_8fbd963c21cad7918e2e14be9f25828c_0bcd594c05270c784251435f39c1b019

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 provides a presumptive diagnosis of pregnancy

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