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Dengue virus Antigen test reagent and kit - India CDSCO Medical Device Registration

Dengue virus Antigen test reagent and kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000088_82845db72bc04168c5c62563dd170096_f38a6f9fae4a7b91c7e95852062067c1. This device is marketed under the brand name ANGCARD. The license holder is Angstrom Biotech Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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 C
Dengue virus Antigen test reagent and kit
UID: MFG/MD/2020/000088_82845db72bc04168c5c62563dd170096_f38a6f9fae4a7b91c7e95852062067c1

Brand Name

ANGCARD

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

detection of Dengue virus Antigen in blood/body fluids

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