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Flo F3 Procedure Pack

by GBUK Group EUDAMED

Active European Union

Ref B-Flo-F3KIT

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506040574FloF3KitFR Basic UDI-DIDate9 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Flo F3 Procedure Pack
Model / Reference
B-Flo-F3KIT
Primary DI / UDI-DI
05060405747929
Basic UDI-DI
506040574FloF3KitFR
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
Procedure Pack intended for patient handling in accordance with manufacturer's assigned intended use / instructions.

Manufacturer details

EUDAMED SRN
UK-PR-000039866

Other devices from GBUK Group, Ltd.

See all devices from GBUK Group, Ltd. →

Properties

Other properties (1)

  • Sterile: No