Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

H.Pylori(HP) Antibody Rapid Test Device (whole blood/serum/plasma)

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

Basic Information

Primary DI
06976753474457
Basic UDI-DI Code
B-06976753474457
Reference
D070501D
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

H.Pylori(HP) Antibody Rapid Test Device (whole blood/serum/plasma) is a rapid chromatographic immunoassay for the qualitative detection of H. pylori Antibodies in human whole blood/serum/plasma.

CND Nomenclature Codes

Code Description
W0105010401 H. PYLORI ANTIGEN DETECTION

Similar Devices

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

View all