CDSCO UID MFG/IVD/2023/000020_be3deebeaf3c3bbca746363ba68cc1a1_fa5e492113939d89d989f98328feb573
SARS-CoV-2: Rapid Antigen Test
Koshbio Private Limited·Device Class Class C·India CDSCO
Registration details
- UID
- MFG/IVD/2023/000020_be3deebeaf3c3bbca746363ba68cc1a1_fa5e492113939d89d989f98328feb573
- Device class
- Class C
- License holder
- Koshbio Private Limited
- Approving authority
- Sub Zonal Baddi
- Product information
- SARS-CoV-2: Rapid Antigen Test is a rapid immunoassay for the qualitative detection of antigen of corona virus (NA) in human nasopharyngeal swab specimen to an aid in the diagnosis of infection with corona virus (NA). For in-vitro diagnostic use only.
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About this record
SARS-CoV-2: Rapid Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000020_be3deebeaf3c3bbca746363ba68cc1a1_fa5e492113939d89d989f98328feb573. The license holder is Koshbio Private Limited, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.
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