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Bone Plates

by Stryker Trauson (Changzhou) Medical Technology Co., Ltd. EUDAMED

Withdrawn No longer placed on the EU market

Ref 21002112EModel Proximal Lateral Tibia Plate I (Stainless Steel),11H, R

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06931720411392 Basic UDI-DIDate16 Aug 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Withdrawn

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.

Specification

EUDAMED

Device Name
Proximal Lateral Tibia Plate I (Stainless Steel),11H, R
Model / Reference
Proximal Lateral Tibia Plate I (Stainless Steel), 11H, R, 21002112E
Primary DI / UDI-DI
06931720411392
Basic UDI-DI
B-06931720411392
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

Other devices from Stryker Trauson (Changzhou) Medical Technology Co., Ltd.

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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