CDSCO UID MFG/IVD/2020/000060_f52e524b4f4ae732dc225f15e98af117_8a209d1f36731e60b2a30ffd5a37b64b
Glanders Antibody detection Rapid Test Kit
Genomix Molecular Diagnostics Pvt Ltd·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2020/000060_f52e524b4f4ae732dc225f15e98af117_8a209d1f36731e60b2a30ffd5a37b64b
- Device class
- Class B
- License holder
- Genomix Molecular Diagnostics Pvt Ltd
- Approving authority
- Telangana
- Product information
- for the qualitative detection of Glanders Specific antibodies in Whole blood, Serum or plasma
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About this record
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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