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MERS -CoV RT-PCR Kit 1.0 - India CDSCO Medical Device Registration

MERS -CoV RT-PCR Kit 1.0 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000143_ec7de552f427eb54cacdb220b0e9e5af_a8797691d47283b4e7f05b4d639fa090. This device is marketed under the brand name AltoStar®. The license holder is Altona Diagnostics India 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
MERS -CoV RT-PCR Kit 1.0
UID: IMP/IVD/2020/000143_ec7de552f427eb54cacdb220b0e9e5af_a8797691d47283b4e7f05b4d639fa090

Brand Name

AltoStar®

Device Class

Class C

Approving Authority

CDSCO

Product Information

The RealStar® MERS-CoV RT-PCR Kit 1.0 is an in vitro diagnostic test, based on real-time PCR technology, for the qualitative detection of Middle East respiratory syndrome coronavirus (AltoStar®) specific RNA

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