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EZy-Rad Pro

by Shimadzu Corporation 10 variants

Ref 566-17900-04

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04540217050314 Basic UDI-DI 04540217050314UDI-DIDate20 Mar 2023RegisteredStatusActive

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  • Withdrawn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
GENERAL RADIOGRAPHIC SYSTEM EZy-Rad Pro
Model / Reference
566-17900-04
Primary DI / UDI-DI
04540217050314
Basic UDI-DI
B-04540217050314
EMDN Code
Z11030506 Teleradiographs
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000025145
Authorised representative
Shimadzu Europa GmbH DE-AR-000013563

Other devices from Shimadzu Corporation

See all devices from Shimadzu Corporation →

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