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A. V. Fistula Sets GF-2217E

by Sb-Kawasumi Laboratories, Inc.

Ref GF-2217EModel A. V. Fistula Sets GF-2217E

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04987488869694 Basic UDI-DI 04987488869694UDI-DIDate11 May 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
A. V. Fistula Sets GF-2217E
Model / Reference
A. V. Fistula Sets GF-2217E, GF-2217E
Primary DI / UDI-DI
04987488869694
Basic UDI-DI
B-04987488869694
EMDN Code
A010401 Arteriovenous fistula needles
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
JP-MF-000011253
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from Sb-Kawasumi Laboratories, Inc.

See all devices from Sb-Kawasumi Laboratories, Inc. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No