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HBsAg Rapid card test - India CDSCO Medical Device Registration

HBsAg Rapid card test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_668a880b9c99d44b74b1de6b76ada80d_95179bc29bdee0ce9c3d272278d69ed3. 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
HBsAg Rapid card test
UID: MFG/IVD/2022/000085_668a880b9c99d44b74b1de6b76ada80d_95179bc29bdee0ce9c3d272278d69ed3

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

The HBsAg test card is used for rapid visual test for the qualitative detection of presence of HBsAg in Human whole blood /serum/plasma samples

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