Eu Ivdr Eu Ivd Class B On The Market 🇨🇳 China

Adenovirus Rapid Test

Devices (same UDI-DI)
6
Certificates
0
Countries
2
Notified Bodies
0

Basic Information

Primary DI
06936983115902
Basic UDI-DI Code
6970277510000YYT
Reference
IAD-N602J-25
Device Types
Single use
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

The Adenovirus Rapid Test is an in-vitro diagnostic rapid chromatographic immunoassay for the qualitative detection of adenovirus in human feces to aid in the diagnosis of adenovirus infection. The Adenovirus Rapid Test is intended to be used by trained laboratory personnel. For laboratory use only. The test provides preliminary test results. Negative results will not preclude adenovirus infection and they can’t be used as the sole basis for treatment or other management decision. The test is not automated. Not for self-testing use. Not for near-patient use.

CND Nomenclature Codes

Code Description
W0105099099 VIROLOGY - RT & POC - OTHER

Available In Countries

🇩🇪 Germany 🇮🇪 Ireland

Related Devices

The Basic UDI-DI associated with this device has 6 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd Class B) and regulation (EU IVDR).

View all