Pure Global

Dengue NS1 Antigen Rapid Test - India CDSCO Medical Device Registration

Dengue NS1 Antigen Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000041_6f26a121a020fa686ffb156b0379fa4d_1193f5c92d3a138f165440d26ee3d4d2. The license holder is Lab-Care Diagnostics (India) Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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
Dengue NS1 Antigen Rapid Test
UID: MFG/IVD/2020/000041_6f26a121a020fa686ffb156b0379fa4d_1193f5c92d3a138f165440d26ee3d4d2

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Dengue NS1 Ag Rapid Test Kit is intended for qualitative determination of NS1 Ag for dengue virus in human Serum/Plasma /Whole Blood

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand