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Bone Plates

by Stryker Trauson (Changzhou) Medical Technology Co., Ltd. 1,000+ variants

Ref 31012090EModel LC-DCP Plates, Femur (Unalloyed Titanium),9H

Withdrawn No longer placed on the EU market

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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/MDD NumberB-06931720416540 Basic UDI-DIDate16 Aug 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device Name
LC-DCP Plates, Femur (Unalloyed Titanium),9H
Model / Reference
LC-DCP Plates, Femur (Unalloyed Titanium), 9H, 31012090E
Primary DI / UDI-DI
06931720416540
Basic UDI-DI
B-06931720416540
EMDN Code
P09120501 Osteosynthesis compression plates
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
CN-MF-000005689
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

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Properties

  • Implantable
  • Reprocessed

Other properties (11)

  • Sterile: No
  • Reusable: No
  • Contains Latex: 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