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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/2020/000016_29d7463814d520d2ae8973294429919b_91e63d5101239a56dd2bd8bf38efa2c0. This device is marketed under the brand name First View. The license holder is BIOLINE DIAGNOSTICS LLP, 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/2020/000016_29d7463814d520d2ae8973294429919b_91e63d5101239a56dd2bd8bf38efa2c0

Brand Name

First View

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The HIV 1/2 Rapid Device is use for the detection of HIV type 1 and type 2 in human serum, plasma or blood sample.

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