HIV 1&2 RAPID TEST - India CDSCO Medical Device Registration

HIV 1&2 RAPID TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_3ebb567a20b01e3ec6d2a07fb646cd5d_ed2564025a584abd6f4edfdcc3ea228b. This device is marketed under the brand name Rapid Plasma Reagin. The license holder is Voxtur Bio Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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

UID: MFG/IVD/2022/000085_3ebb567a20b01e3ec6d2a07fb646cd5d_ed2564025a584abd6f4edfdcc3ea228b

Brand Name

Rapid Plasma Reagin

License Holder

Voxtur Bio Ltd

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

HIV 1&2 test card is used as Rapid visual test for the Qualitative detection for the presence of HIV 1 and 2 antibodies in Human whole blood serum, plasma samples

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HBsAg ELISA Kit

Brand: Rapid Plasma Reagin

Voxtur Bio Ltd

HIV 1&2 RAPID TEST - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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