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Traumaarm

by Medizintechnik St. Egidien GmbH

Ref 1300, 068

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42607313003T Basic UDI-DI Date1 Oct 2024RegisteredStatusActive

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  • Withdrawn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
Traumaarm
Model / Reference
1300, 068
Primary DI / UDI-DI
04260739620085, 04260739620023
Basic UDI-DI
42607313003T, 426073068N5
Direct Marketing DI
04260739620085
04260739620023
EMDN Code
Z11039080 Various radiodiagnostic and interventional instruments - hardware accessories
Device Class
Class I
EU market of registration
Germany
Austria

Manufacturer details

EUDAMED SRN
DE-MF-000009064

Other devices from Medizintechnik St. Egidien GmbH

See all devices from Medizintechnik St. Egidien GmbH →

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