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FMD DIVA ANTIBODY ELISA KIT - India CDSCO Medical Device Registration

FMD DIVA ANTIBODY ELISA KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_f5562c5b75450e0346785ba8911573ff_7b8a2e1e084ab0b82af3c54549386963. 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
FMD DIVA ANTIBODY ELISA KIT
UID: MFG/IVD/2020/000082_f5562c5b75450e0346785ba8911573ff_7b8a2e1e084ab0b82af3c54549386963

Brand Name

BIOGENIX

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The Foot-and-mouth disease DIVA ELISA Test kit is used for the detection of FMD vaccinated and non-vaccinated animal serum samples with 3ABC antigen

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