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Orthopaedic Wires Power Driven Cobalt Alloy - Single Use

by Synthes GmbH 17 variants

Ref 03.211.435.01S, 310.243, 03.211.430.01, 03.211.425.01S, 03.211.420.01S, 03.211.410.01, 292.619S, 03.211.440.01S, 03.045.018S, 03.010.115, 03.211.415.01S, 03.211.425.01, 357.399Model Orthopaedic Wires Power Driven Cobalt Alloy - Single Use

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 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/MDR Number7611819a00558K8 Basic UDI-DI Date9 Apr 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Orthopaedic Wires Power Driven Cobalt Alloy - Single Use
Model / Reference
Orthopaedic Wires Power Driven Cobalt Alloy - Single Use, 03.211.435.01S, 310.243, 03.211.430.01, 03.211.425.01S, 03.211.420.01S, 03.211.410.01, 292.619S, 03.211.440.01S, 03.045.018S, 03.010.115, 03.211.415.01S, 03.211.425.01, 357.399
Primary DI / UDI-DI
07611819445000, 07611819755116, 07611819435117, 07611819444980, 07611819444973, 07611819435032, 07611819931541, 07611819445017, 07612334180964, 07611819814950, 07611819444966, 07611819435094, 07611819738393
Basic UDI-DI
7611819a00558K8
Direct Marketing DI
07611819755116
07611819814950
07611819738393
EMDN Code
Z12130599 Motorised orthopaedic surgery system instruments - other
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CH-MF-000013345
Authorised representative
DePuy Ireland UC IE-AR-000009328

Other devices from Synthes GmbH

See all devices from Synthes GmbH →

Properties

  • Sterile YesEUDAMEDNoEUDAMED
  • CMR Substance

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No