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Dengue virus Antigen Test Kits - India CDSCO Medical Device Registration

Dengue virus Antigen Test Kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000005_de089c1b77def8ee0aae7045c2bbf384_dea1f45de58b3b08acbb544c3235711e. This device is marketed under the brand name STANDARD Q Dengue NS1 Ag Test, ULTRA Dengue NS1 Ag Test. The license holder is SD Biosensor 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 virus Antigen Test Kits
UID: MFG/MD/2018/000005_de089c1b77def8ee0aae7045c2bbf384_dea1f45de58b3b08acbb544c3235711e

Brand Name

STANDARD Q Dengue NS1 Ag Test, ULTRA Dengue NS1 Ag Test

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

ULTRA Dengue NS1 Ag Test is an immunochromatographic assay for the detection of Dengue NS1 antigen in human serum, plasma or whole blood. The kit is for in vitro use only. This is intended for professional use only for an initial screening test

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DJ Fang

DJ Fang

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