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DIARENNEEDLE AVF 16G VF Sterile Arteriovenous Fistula Needle

by Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş.

Ref DIARENNEEDLE AVF 16G VF

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08697658000258 Basic UDI-DI 08697658000258UDI-DIDate29 Apr 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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Sterile Arteriovenous Fistula Needle
Model / Reference
DIARENNEEDLE AVF 16G VF
Primary DI / UDI-DI
08697658000258
Basic UDI-DI
B-08697658000258
EMDN Code
A010401 Arteriovenous fistula needles
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018494

From the manufacturer

Manufacturer's product page: AV Fistula Needle Set

Other devices from Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş.

See all devices from Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş. →

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