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EIA Antibody Rapid Test Kit - India CDSCO Medical Device Registration

EIA Antibody Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_f729cf4a0609772bb865c66cbbd1119f_9dc2b501d964c145e65096e0b61bd9c7. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
EIA Antibody Rapid Test Kit
UID: MFG/IVD/2020/000060_f729cf4a0609772bb865c66cbbd1119f_9dc2b501d964c145e65096e0b61bd9c7

Device Class

Class B

Approving Authority

Telangana

Product Information

for the qualitative detection of Equine Infectious Anaemia ##PLACEHOLDER_0## Specific antibodies in Whole blood, Serum or plasma

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