SARS CoV-2 Antigen Rapid Test - India CDSCO Medical Device Registration

SARS CoV-2 Antigen Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000057_35c276030c2c161e9dd6e23752c410c9_ce095ee4c54151b33b836ba1b55a5fc5. This device is marketed under the brand name ZyDx Anti-SARS CoV-2-IgG Antibody Detection ELISA. The license holder is Cadila Healthcare Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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