Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

DENGUE - RT & POC

Devices (same UDI-DI)
1
Certificates
0
Countries
13
Notified Bodies
0

Let the assistant research this device

The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.

Free to try · every answer cites its records

Basic Information

Primary DI
D-000041242DEN003-256L
Basic UDI-DI Code
B-000041242DEN003-256L
Reference
DEN003-25
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The Dengue IgG/IgM+NS1 Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of Dengue virus IgG/lgM antibody and NS1antigen in human serum plasma or whole blood. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Dengue viruses.

CND Nomenclature Codes

Code Description
W0105099007 DENGUE - RT & POC

Available In Countries

🇧🇬 Bulgaria 🇨🇾 Cyprus 🇩🇪 Germany 🇪🇪 Estonia 🇭🇷 Croatia 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇷🇴 Romania 🇸🇮 Slovenia 🇸🇰 Slovakia

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).

View all