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Allengers

by Allengers Medical Systems Limited 26 variants

Ref AMSL/UM/HF59PLUS/XX/60Model HF59Plus

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-08904139700027 Basic UDI-DI 08904139700027UDI-DIDate22 Aug 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  • Withdrawn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
Hf C-Arm
Model / Reference
HF59Plus, AMSL/UM/HF59PLUS/XX/60
Primary DI / UDI-DI
08904139700027
Basic UDI-DI
B-08904139700027
EMDN Code
Z11039017 Mobile radioscopic units
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IN-MF-000032921
Authorised representative
Easy Medical Device CommV BE-AR-000011902

Other devices from Allengers Medical Systems Limited

See all devices from Allengers Medical Systems Limited →

Properties

Other properties (11)

  • Sterile: No
  • 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