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Dengue NS1 Antigen Rapid Test Device - India CDSCO Medical Device Registration

Dengue NS1 Antigen Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_9437cdd9d7123b03533a2624033b75b8_2c71020cfa6bad869bc7282e5ab63956. This device is marketed under the brand name CRP. The license holder is BIOLINE DIAGNOSTICS LLP, 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 NS1 Antigen Rapid Test Device
UID: MFG/IVD/2020/000016_9437cdd9d7123b03533a2624033b75b8_2c71020cfa6bad869bc7282e5ab63956

Brand Name

CRP

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Dengue NS1Antigen Rapid Test Device is a rapid and convenient immunochromatographic in vitro assay for detection of Dengue NS1 Antigen in human serum, plasma. The test provides a visual, qualitative result, and all positive specimens are advised to be confirmed with other qualified assays

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