Skip to content

Gelenkarm

by mediPlac GmbH 2 variants

Ref 300.088-02GModel 300.400*

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, self-declared

Class I: no certifier involved

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 Number4064551mP022XB Basic UDI-DI 04064551001325UDI-DIDate2 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Gelenkarm
Model / Reference
300.400*, 300.088-02G
Primary DI / UDI-DI
04064551001325
Basic UDI-DI
4064551mP022XB
EMDN Code
Z12011299 Patient positioning instruments – other
Device Class
Class I
Medical Purpose
Lagerungssystem zur Positionierung und/oder Fixierung von Patienten

Manufacturer details

EUDAMED SRN
DE-PR-000046145

Other devices from mediPlac GmbH

See all devices from mediPlac GmbH →

Properties

Other properties (1)

  • Sterile: No