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Mycoplasma pneumoniae PCR Kit - India CDSCO Medical Device Registration

Mycoplasma pneumoniae PCR Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000072_39fef7c0a37a513d21ade332eddb8d52_8bd09fa051ef59d37ebc371ccaaf7ee8. 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
Mycoplasma pneumoniae PCR Kit
UID: IMP/IVD/2019/000072_39fef7c0a37a513d21ade332eddb8d52_8bd09fa051ef59d37ebc371ccaaf7ee8

Brand Name

Geneproof

License Holder

ADT India Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

The PCR kit is designed for Mycoplasma pneumoniae detection by the real-timePolymerase Chain Reaction (Geneproof) method

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