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Human Immunodeficiency Virus – Rapid - India CDSCO Medical Device Registration

Human Immunodeficiency Virus – Rapid is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000009_52022eeeaf25ad89850cd7f0e52e53e8_946dfe4540f47003d986d2b9eef5e2e0. This device is marketed under the brand name HIV. The license holder is Vimek Bioconcept Pvt Ltd, and it is classified as Device Class Class D. The approving authority is DSM Nutritional Products India Pvt. Ltd..

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
Human Immunodeficiency Virus – Rapid
UID: MFG/IVD/2022/000009_52022eeeaf25ad89850cd7f0e52e53e8_946dfe4540f47003d986d2b9eef5e2e0

Brand Name

HIV

Device Class

Class D

Approving Authority

DSM Nutritional Products India Pvt. Ltd.

Product Information

A Human Immunodeficiency Virus – (HIV) test reagent/kit is medical device intended for the detection of Human Immunodeficiency Virus – (HIV) in Blood/serum/Plasma/body fluids.

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