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CEA Rapid Quantitative Test (Chemiluminescence Immunoassay)

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

Basic Information

Primary DI
06933260207213
Basic UDI-DI Code
B-06933260207213
Reference
BT0505705
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

It is used for in vitro quantitative detection of the Carcinoembryonic antigen (CEA) concentration in human serum, plasma that contains heparin /EDTA and other anticoagulants and venous whole blood samples, mainly used for auxiliary diagnosis of cancer patients.

CND Nomenclature Codes

Code Description
W0102030112 CARCINOEMBRYONIC ANTIGEN

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