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COVID-19 kit - India CDSCO Medical Device Registration

COVID-19 kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000072_30f820d26d41b86c88eb632b760da237_f8d63013139f87b008e1ad00cc4c7c68. This device is marketed under the brand name Geneproof. The license holder is ADT 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
COVID-19 kit
UID: IMP/IVD/2019/000072_30f820d26d41b86c88eb632b760da237_f8d63013139f87b008e1ad00cc4c7c68

Brand Name

Geneproof

License Holder

ADT India Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

The PCR kit is intended for detection of SARS-CoV-2, by the reverse transcription real-time Polymerase Chain Reaction (Geneproof) method. The SARS-CoV-2 detection consists in amplification of specific region in RdRp gene, E gene and N gene

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