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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 IMP/IVD/2020/000315_ba61bb8f69e2508278637067c3e2f36d_2463fe691d6c64241371e654528809ba. This device is marketed under the brand name Promotor. The license holder is DEEP MEDITECH PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.

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
SARS-CoV-2 Antigen Rapid Test
UID: IMP/IVD/2020/000315_ba61bb8f69e2508278637067c3e2f36d_2463fe691d6c64241371e654528809ba

Brand Name

Promotor

Device Class

Class C

Approving Authority

CDSCO

Product Information

A rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasal and nasopharyngeal swab specimens

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