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G-Flex Europe

Country not established FDA

Part of G-Flex Europe SRL

Devices
0
Registrations
FDA
FDA recalls
0

No devices from this company are in the catalogue yet.

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

Company details

DUNS number
763193690

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • G-Flex Europe SRL Nivelles Brabant Wallon · BE FEI 3008274780