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CDSCO UID MFG/IVD/2021/000124_64fcce6f7406c24b9d0227d1b69d0921_7c1f12c628e0d8b6262a3be976fadd40

Antigen Rapid Detection Test Kit

LORVEN BIOLOGICS PRIVATE LIMITED·Device Class Class C·India CDSCO·Brand: Lorven
Registration details
UID
MFG/IVD/2021/000124_64fcce6f7406c24b9d0227d1b69d0921_7c1f12c628e0d8b6262a3be976fadd40
Device class
Class C
Brand name
Lorven
License holder
LORVEN BIOLOGICS PRIVATE LIMITED
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.
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About this record

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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