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XL-Platen D RADIUS 1

by ProMedionics

Ref XL-Platen D RADIUS 1

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5430002824UARMSQ Basic UDI-DI 05430005383252UDI-DIDate3 Sep 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Upper-arm
Model / Reference
XL-Platen D RADIUS 1
Primary DI / UDI-DI
05430005383252
Basic UDI-DI
5430002824UARMSQ
EMDN Code
P09120503 Osteosynthesis screw-plate systems
Device Class
Class IIb
Medical Purpose
Osteosynthesis Upper-arm

Manufacturer details

EUDAMED SRN
BE-PR-000054323

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Properties

Other properties (1)

  • Sterile: No