Antigen Rapid Detection Test Kit - India CDSCO Medical Device Registration
Antigen Rapid Detection Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000124_64fcce6f7406c24b9d0227d1b69d0921_7c1f12c628e0d8b6262a3be976fadd40. This device is marketed under the brand name Lorven. The license holder is LORVEN BIOLOGICS PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.
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Brand Name
Lorven
License Holder
LORVEN BIOLOGICS PRIVATE LIMITEDDevice Class
Approving Authority
CDSCO, Zonal office, Hyderabad
Product Information
Intended for qualitative detection of COVID-19 antigen (Lorven) from nasal swab, nasopharyngeal swab, endotracheal aspirate or Broncho alveolar lavage obtained from patient with signs and symptoms of respiratory infection.
