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Diagnostics Rapid test reagent/ kits for Dengue IgG/IgM - India CDSCO Medical Device Registration

Diagnostics Rapid test reagent/ kits for Dengue IgG/IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000160_00a9f248f4dd88cbf8c06c98bebb7541_e082e96c06f012143899e4865401027b. The license holder is Alpine Biomedicals Private Limited, and it is classified as Device Class Class B. The approving authority is Haryana.

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 B
Diagnostics Rapid test reagent/ kits for Dengue IgG/IgM
UID: MFG/IVD/2022/000160_00a9f248f4dd88cbf8c06c98bebb7541_e082e96c06f012143899e4865401027b

Device Class

Class B

Approving Authority

Haryana

Product Information

Rapid Dengue Antibody test reagent/ kit is a medical device intended for the detection of Dengue Antibody in blood/serum/plasma

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