Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

SARS-CoV-2/Flu A+B/AdV/RSV Antigen Rapid Test

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

Basic Information

Primary DI
06935091671973
Basic UDI-DI Code
B-06935091671973
Reference
/
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The SARS-CoV-2/Flu A+B/AdV/RSV Antigen Rapid Test is intended for in vitro qualitative detection to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen, influenza A+B (Flu A+B) antigen, respiratory adenovirus (AdV) antigen and respiratory syncytial virus (RSV) antigen in human nasopharyngeal swab or oropharyngeal swab samples.

CND Nomenclature Codes

Code Description
W0105099099 VIROLOGY - RT & POC - OTHER

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