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Dengue Antigen Ns1 TEST KIT - India CDSCO Medical Device Registration

Dengue Antigen Ns1 TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000041_2748dee59a0b5d05a410c957f17ebe33_8f269fb584ea115133249f9631594317. This device is marketed under the brand name TurbiMAX & OEM. The license holder is Avecon Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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 Antigen Ns1 TEST KIT
UID: MFG/IVD/2019/000041_2748dee59a0b5d05a410c957f17ebe33_8f269fb584ea115133249f9631594317

Brand Name

TurbiMAX & OEM

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

Dengue NS1 is a rapid Immunochromatographic assay for the Qualitative detection of Non-structural protein 1(TurbiMAX & OEM) in human serum/plasma/Whole Blood

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