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SARS-CoV-2 RT-PCR - India CDSCO Medical Device Registration

SARS-CoV-2 RT-PCR is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000085_58d898d79de35d806698714521ebb4c1_f945ad824bd11953ff7f9630ed031c55. This device is marketed under the brand name CLIA. The license holder is DIAGNOSTIC CARE AND TRADING 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 RT-PCR
UID: IMP/IVD/2021/000085_58d898d79de35d806698714521ebb4c1_f945ad824bd11953ff7f9630ed031c55

Brand Name

CLIA

Device Class

Class C

Approving Authority

CDSCO

Product Information

The SARS-CoV-2 RT-PCR Assay is used for qualitative detection of SARS-CoV-2 from oropharyngeal swabs, nasopharyngeal swabs and BALF (CLIA) of suspected cases of COVID-19.

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