Skip to content

AV Fistula Needle Set

by Disposafe Health & Lifecare Limited 16 variants

Ref AVF173

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-AVF173 Basic UDI-DI AVF173UDI-DIDate12 Oct 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  • Withdrawn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
AV Fistula 17G Back cut needle Rotating wings
Model / Reference
AVF173
Primary DI / UDI-DI
AVF173
Basic UDI-DI
B-AVF173
EMDN Code
A010401 Arteriovenous fistula needles
Device Class
Class IIa
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
IN-MF-000020265
Authorised representative
AR Experts B.V. NL-AR-000023989

Other devices from Disposafe Health & Lifecare Limited

See all devices from Disposafe Health & Lifecare Limited →

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