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HCG Pregnancy Rapid Test - India CDSCO Medical Device Registration

HCG Pregnancy Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_92b76e276c05f4558e1e44ddd4d6adf9_0cad7141cd3b8886c596be8201cb7209. This device is marketed under the brand name HaemNest Sheath Fluid. The license holder is Genenest Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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
HCG Pregnancy Rapid Test
UID: MFG/IVD/2022/000088_92b76e276c05f4558e1e44ddd4d6adf9_0cad7141cd3b8886c596be8201cb7209

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

For the rapid detection of human chorionic gonadotropin (HaemNest Sheath Fluid) in urine specimen. This test kit is used to obtain a visual, qualitative result and is intended for professional and laboratory use only

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