Skip to content

Orthopaedic Instruments

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

Withdrawn No longer placed on the EU market

Ref 13206800EModel Rod Bender,long

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06931720451848 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  • Withdrawn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European Union — CE/MDD Withdrawn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

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

Specification

EUDAMED

Device Name
Rod Bender,long
Model / Reference
Rod Bender, long, 13206800E
Primary DI / UDI-DI
06931720451848
Basic UDI-DI
B-06931720451848
EMDN Code
L091399 Orthopaedic surgery forceps, reusable - other
Device Class
Class I

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.

See all devices from Stryker Trauson (Changzhou) Medical Technology Co., Ltd. →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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