S.Typhi-paratyphi antigen card test - India CDSCO Medical Device Registration

S.Typhi-paratyphi antigen card test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000018_bd069f503230107e9a10a488178ab211_ca009cfb4d0c8c98b91a0a9d17b12068. This device is marketed under the brand name PT. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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 C

S.Typhi-paratyphi antigen card test

UID: MFG/IVD/2022/000018_bd069f503230107e9a10a488178ab211_ca009cfb4d0c8c98b91a0a9d17b12068

Brand Name

PT

License Holder

Beacon Diagnostics Pvt. Ltd.

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

For the qualitative detection of S. typhi and paratyphi antigen in human serum / feaces

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