Pure Global

Diagnostics Rapid test reagent/ kits for Dengue NS1. - India CDSCO Medical Device Registration

Diagnostics Rapid test reagent/ kits for Dengue NS1. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000064_4d8a2fbe795b0d4a2ccfdd9fabf4ce80_dcde0bb1524dd1bfa5692947ae28a300. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class C. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Diagnostics Rapid test reagent/ kits for Dengue NS1.
UID: MFG/IVD/2022/000064_4d8a2fbe795b0d4a2ccfdd9fabf4ce80_dcde0bb1524dd1bfa5692947ae28a300

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Dengue virus Antigen test reagent/ kit is a medical device intended for the detection of Dengue Antigen in Serum, Plasma, blood with lateral flow assay

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing