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Covid-19 Rapid Antigen Test Kit - India CDSCO Medical Device Registration

Covid-19 Rapid Antigen Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000075_76e21f092f8c9c01133f3ddb3be8df3f_29bc5246eec66458b90063dab32eeab2. This device is marketed under the brand name InstaCOVID Ag. The license holder is ANAMOL LABORATORIES PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West 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.

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CDSCO Registered
Class Class C
Covid-19 Rapid Antigen Test Kit
UID: MFG/IVD/2022/000075_76e21f092f8c9c01133f3ddb3be8df3f_29bc5246eec66458b90063dab32eeab2

Brand Name

InstaCOVID Ag

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Qualitative detection of specific antigen to SARS CoV-2 present in human nasopharynx

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