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COVID-19 Real Time PCR Kit - India CDSCO Medical Device Registration

COVID-19 Real Time PCR Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000112_bdd2dba94c8644c78c30bf48d793a7f7_e6e3fd1bee583778439f557545d9c05a. This device is marketed under the brand name Lyo Mix. The license holder is Genetix Biotech Asia 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
COVID-19 Real Time PCR Kit
UID: MFG/IVD/2020/000112_bdd2dba94c8644c78c30bf48d793a7f7_e6e3fd1bee583778439f557545d9c05a

Brand Name

Lyo Mix

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

COVI-quick is a real time PCR based diagnostic kit for the qualitative detection of novel coronavirus SARS Cov-2 RNA from Nasopharyngeal, oropharyngeal, swabs and sputum samples from patients. COVI-quick with its unique inhibitor tolerant properties allows amplification of difficult samples, whereas, its fast cycling properties help reduce turn around time in less than one hour

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