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Dengue NS-1 Antigen Test - India CDSCO Medical Device Registration

Dengue NS-1 Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000024_f998b7eba56878f94092798a575998fb_f0292feda2acb18913e948f697689c78. This device is marketed under the brand name TRURAPID® Dengue NS-1 Ag Test. The license holder is KILPEST INDIA LIMITED, 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.

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CDSCO Registered
Class Class C
Dengue NS-1 Antigen Test
UID: MFG/IVD/2020/000024_f998b7eba56878f94092798a575998fb_f0292feda2acb18913e948f697689c78

Brand Name

TRURAPID® Dengue NS-1 Ag Test

License Holder

KILPEST INDIA LIMITED

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

TRURAPID® Dengue NS-1 Ag Test is an in-vitro diagnostic lateral flow immunoassay intended for the qualitative detection of Dengue NS1 Antigen in human serum/ plasma

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