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HEMO PHENIX A.V. Fistula Needle Set

by JMS Singapore Pte Ltd 16 variants

Ref V17R20-30SP+Model 862-1726

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-862-1726AZ Basic UDI-DI D-862-1726AZUDI-DIDate30 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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Hemo Phenix Avf
Model / Reference
862-1726, V17R20-30SP+
Primary DI / UDI-DI
D-862-1726AZ
Basic UDI-DI
B-862-1726AZ
EMDN Code
A010401 Arteriovenous fistula needles
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
SG-MF-000024704
Authorised representative
Bionic Medizintechnik GmbH DE-AR-000012049

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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