Dengue NS1 Rapid Antigen Test - India CDSCO Medical Device Registration

Dengue NS1 Rapid Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000057_7b2548ce54951d0031cf42487d2ca6f7_a1a6a9a9f198a39daff336305598ad8d. 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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