COVID-19 Ag Test - India CDSCO Medical Device Registration
COVID-19 Ag Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000095_f7985e36bfdeef05bcc83952e913f945_bffbe79495ade2cbe2890eb1e2d847a3. This device is marketed under the brand name Sensit Rapid. The license holder is Ubio Biotechnology Systems Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Brand Name
Sensit Rapid
License Holder
Ubio Biotechnology Systems Private LimitedDevice Class
Approving Authority
Central Drug Standard Control Organisation, South Zone
Product Information
COVID-19 Ag Test kit is an IVD medical device intended for the qualitative detection of SARS-COV2 antigen in human nasopharyngeal or throat specimen, which indicates COVID-19 infection
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