HCG RAPID TEST - India CDSCO Medical Device Registration

HCG RAPID TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_ecac5115c5bc9a5c3c39d26a90ec6a19_8123a9b2ebb3fa9b2317ce8b16d7074d. This device is marketed under the brand name BIOGENIX. The license holder is Biogenix Inc. 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 RAPID TEST

UID: MFG/IVD/2020/000082_ecac5115c5bc9a5c3c39d26a90ec6a19_8123a9b2ebb3fa9b2317ce8b16d7074d

Brand Name

BIOGENIX

License Holder

Biogenix Inc. Pvt. Ltd.

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

For detection of pregnancy (BIOGENIX) in human urine

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FT3 CLIA Test Reagent Kit

Brand: BIOGENIX

Biogenix Inc. Pvt. Ltd.

HCG RAPID TEST - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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