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ProGRP Rapid Quantitative Test (Chemiluminescence Immunoassay)

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

Basic Information

Primary DI
06933260206834
Basic UDI-DI Code
B-06933260206834
Reference
BT0505102
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 Progastrin-releasing peptide (ProGRP) concentration in human serum, plasma that contains heparin /EDTA and other anticoagulants and venous whole blood samples, mainly supports differential diagnosis in lung cancer.

CND Nomenclature Codes

Code Description
W0102039099 TUMOUR MARKERS - OTHER

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