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/2022/000056_6f26a121a020fa686ffb156b0379fa4d_23eb4c1731f83a23cb3216bf0347a5c1. The license holder is Biotrol Laboratories Pvt. Ltd., 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Dengue NS1 Antigen Rapid Test
UID: MFG/IVD/2022/000056_6f26a121a020fa686ffb156b0379fa4d_23eb4c1731f83a23cb3216bf0347a5c1

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Dengue NS1 Antigen Rapid Test device is a qualitative test for the detection of NS1 Antigen to dengue virus in human serum, plasma, or whole blood. This test is for In-Vitro Diagnostic use only

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

Dengue NS1 Antigen Rapid Test

Lab-Care Diagnostics (India) Pvt. Ltd.

Class C
Other Products from Biotrol Laboratories Pvt. Ltd.
Products from the same license holder (10 products)

H. Pylori Ag Rapid Test

Class C

Procalcitonin Ag Rapid Test

Class C

HBsAg Rapid Test

Class D

Vibrio Cholera Ag Rapid Test

Class C

Malaria PF/PAN Ag Rapid Test

Class C

Troponin I Rapid Test

Class C

Rotavirus Antigen Rapid Test

Class C

Rota and Adenovirus Antigen Rapid Test Kit

Class C

HIV 1/2 Rapid Test Device

Class D

HCV Rapid Test

Class D