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Rota and Adenovirus Antigen Rapid Test Kit - India CDSCO Medical Device Registration

Rota and Adenovirus Antigen Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_39302da3333f8511c3ee5e604b15b0c8_4c67f45d60c652ec90c5f24e1b37a489. The license holder is Biotrol Laboratories 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
Rota and Adenovirus Antigen Rapid Test Kit
UID: MFG/IVD/2022/000056_39302da3333f8511c3ee5e604b15b0c8_4c67f45d60c652ec90c5f24e1b37a489

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Rota and Adenovirus Antigen Rapid Test Kit is a lateral flow chromatographic immunoassay for the qualitative detection of Rota virus and Adenovirus in human Fecal Specimen

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