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PG I Rapid Quantitative Test (Chemiluminescence Immunoassay)

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

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Basic Information

Primary DI
06933260207008
Basic UDI-DI Code
B-06933260207008
Reference
BT0505304
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 Pepsinogen I (PG I) concentration in human serum, plasma that contains sodium citrate and EDTA anticoagulants samples, mainly used for auxiliary diagnosis of gastrin diseases.

CND Nomenclature Codes

Code Description
W0102039099 TUMOUR MARKERS - OTHER

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