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Rotanode Xrc-2451X

by Canon Electron Tubes & Devices Co., Ltd.

Model X-ray Tube Assembly

Active European Union

CE MDR

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/MDR Number45802744133523659295537M9 Basic UDI-DI 04580274413714UDI-DIDate22 Apr 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
X-ray Tube Assembly
Primary DI / UDI-DI
04580274413714
Basic UDI-DI
45802744133523659295537M9
EMDN Code
Z11039012 X-ray tube assembly
Device Class
Class IIb
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
JP-MF-000009481
Authorised representative
Canon Medical Components Europe B.V. NL-AR-000029305

Other devices from Canon Electron Tubes & Devices Co., Ltd.

See all devices from Canon Electron Tubes & Devices Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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