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( BAYFLEX ) AV FISTÜLA IĞNESI (ARTER), Uzunluk : 25 cm (Size 16 G)

by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

Ref BF 9003-16-25-AModel ULTRAMED A.V. FISTULA NEEDLE, ( BAYFLEX ) AV FISTÜLA IĞNESI (ARTER), Uzunluk : 25 cm (Size 16 G)

Active European Union

CE MDR 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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number622300425AVF9003RQ Basic UDI-DI 06223004259784UDI-DIDate9 Mar 2026RegisteredStatusActive
European UnionCE/MDR Number622300425AVF9003RQ Basic UDI-DI 06223004259784UDI-DIDate9 Mar 2026RegisteredStatusActive

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  • Withdrawn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, CE/MDR Active

Specification

EUDAMED

Device Name
Ultramed A.V. Fistula Needle
Model / Reference
ULTRAMED A.V. FISTULA NEEDLE, BF 9003-16-25-A, ( BAYFLEX ) AV FISTÜLA IĞNESI (ARTER), Uzunluk : 25 cm (Size 16 G)
Primary DI / UDI-DI
06223004259784
Basic UDI-DI
622300425AVF9003RQ, B-06223004259784
EMDN Code
A010401 Arteriovenous fistula needles
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
EG-MF-000038562
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

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Properties

  • Sterile

Other properties (12)

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