CDSCO UID MFG/IVD/2020/000060_f729cf4a0609772bb865c66cbbd1119f_9dc2b501d964c145e65096e0b61bd9c7
EIA Antibody Rapid Test Kit
Genomix Molecular Diagnostics Pvt Ltd·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2020/000060_f729cf4a0609772bb865c66cbbd1119f_9dc2b501d964c145e65096e0b61bd9c7
- Device class
- Class B
- License holder
- Genomix Molecular Diagnostics Pvt Ltd
- 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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About this record
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.
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