Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

IgE Rapid Test Device (whole blood/serum/plasma)

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

Basic Information

Primary DI
06976753472927
Basic UDI-DI Code
B-06976753472927
Reference
D020501D
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The IgE Rapid Test is for the qualitative detection of human IgE antibody in whole blood, serum or plasma as an aid in the diagnosis of allergy.

CND Nomenclature Codes

Code Description
W0102010199 IMMUNOGLOBULINS - OTHER

Similar Devices

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

View all