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HIV 1/2 Rapid Test Device - India CDSCO Medical Device Registration

HIV 1/2 Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_29d7463814d520d2ae8973294429919b_5c34b6765e42592c211edfd507a2ed25. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class D. 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 D
HIV 1/2 Rapid Test Device
UID: MFG/IVD/2022/000056_29d7463814d520d2ae8973294429919b_5c34b6765e42592c211edfd507a2ed25

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The HIV 1/2 Rapid test is an immunochromatographic assay used for qualitative detection for HIV in human specimen

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