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HIV 1 &2 Ag-Ab ELISA detection Kit - India CDSCO Medical Device Registration

HIV 1 &2 Ag-Ab ELISA detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_5082efc182741a4a83389f5ccdea9cd7_8124f897f79d49ec6a3ac6e1bbc3496f. 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 Ag-Ab ELISA detection Kit
UID: MFG/IVD/2022/000085_5082efc182741a4a83389f5ccdea9cd7_8124f897f79d49ec6a3ac6e1bbc3496f

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

ELISA- Enzyme Linked Immunosorbent Assay kit for the detection of Antibodies to HIV 1,antigens to HIV1 (Rapid Plasma Reagin) and antibodies to HIV 2 (Rapid Plasma Reagin) in Human Serum/Plasma

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