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Glanders Antibody detection Rapid Test Kit - India CDSCO Medical Device Registration

Glanders Antibody detection Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_f52e524b4f4ae732dc225f15e98af117_8a209d1f36731e60b2a30ffd5a37b64b. 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
Glanders Antibody detection Rapid Test Kit
UID: MFG/IVD/2020/000060_f52e524b4f4ae732dc225f15e98af117_8a209d1f36731e60b2a30ffd5a37b64b

Device Class

Class B

Approving Authority

Telangana

Product Information

for the qualitative detection of Glanders Specific antibodies in Whole blood, Serum or plasma

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