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HIV I & II Ab RAPID TEST - India CDSCO Medical Device Registration

HIV I & II Ab RAPID TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000055_7e8e404edb0de8d29d423e2e087aef70_7aef509772b9250d7c32818db952d5e7. This device is marketed under the brand name LIFELINE. The license holder is Rapha Diagnostics Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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 I & II Ab RAPID TEST
UID: MFG/IVD/2021/000055_7e8e404edb0de8d29d423e2e087aef70_7aef509772b9250d7c32818db952d5e7

Brand Name

LIFELINE

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

LIFELINE HIV I & II Ab Rapid Test is a colloidal gold enhanced, rapid immunochromatographic assay for the qualitative detection of antibodies to human immunodeficiency virus (LIFELINE) in human serum or plasma

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