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IBR Antibody Rapid Test Kit - India CDSCO Medical Device Registration

IBR Antibody Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_ece33b0632f28a5467c53a3611f37321_ed1f0e94ef100db3889b7fa62dbbdaaa. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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CDSCO Registered
Class Class B
IBR Antibody Rapid Test Kit
UID: MFG/IVD/2020/000060_ece33b0632f28a5467c53a3611f37321_ed1f0e94ef100db3889b7fa62dbbdaaa

Device Class

Class B

Approving Authority

Telangana

Product Information

For in-vitro detection of Bovine Herpes Virus-1 ##PLACEHOLDER_0## specific antibodies in whole blood, serum or plasma with clinical symptoms in consistent with Infectious bovine rhinotracheitis ##PLACEHOLDER_0##

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