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

HIV 1/2 Antibody Detection Rapid Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_766e8b6822857255dc05042ff8a3f826_463db2c241f0b0fc8d83b1aebebacec8. The license holder is Levram Lifesciences Private Limited, 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 Antibody Detection Rapid Test kit
UID: MFG/IVD/2022/000109_766e8b6822857255dc05042ff8a3f826_463db2c241f0b0fc8d83b1aebebacec8

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Rapid Test for detection and differentiation of antibodies to HIV 1 and HIV 2 from human serum/plasma/whole blood

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