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Corona Antigen test - India CDSCO Medical Device Registration

Corona Antigen test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000078_909ab25eac1c180ba4b1fd3437661928_c73eef124a67b2e78341b21e53cffb4a. This device is marketed under the brand name identi SARS-CoV-2 RT PCR. The license holder is Oscar Medicare Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Corona Antigen test
UID: MFG/IVD/2020/000078_909ab25eac1c180ba4b1fd3437661928_c73eef124a67b2e78341b21e53cffb4a

Brand Name

identi SARS-CoV-2 RT PCR

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

OSCAR Corona Antigen test is a one-step rapid, qualitative, sandwich immunoassay. It is used for the detection of N antigen of corona virus in human nasopharyngeal swab specimen. For professional use only

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