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PG I/PGII/G17 Rapid Quantitative Test

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

Basic Information

Primary DI
06933260207947
Basic UDI-DI Code
B-06933260207947
Reference
BT0200601
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The Biotime PGI/PGII/G17 Rapid Quantitative Test along with Biotime FIA Analyzer is intended to use for in vitro quantitative determination of the concentration of pepsinogen I/pepsinogen II/gastrin 17 in human serum, plasma or venous whole blood.

CND Nomenclature Codes

Code Description
W0102039099 TUMOUR MARKERS - OTHER

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