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Cabo de Chave Fixo - Sistema 2, 4mm

by DELPHOS IMPLANTS - Indústria, Comércio, Importação e Exportação de Implantes Médicos, S.A.

Ref DA-0019-810

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56004617INST02G3 Basic UDI-DI 05600461725693UDI-DIDate9 Jun 2026RegisteredStatusActive

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  • Withdrawn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
Screwdriver Handle
Model / Reference
DA-0019-810
Primary DI / UDI-DI
05600461725693
Basic UDI-DI
56004617INST02G3
EMDN Code
L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
PT-MF-000012964

Other devices from DELPHOS IMPLANTS – Indústria, Comércio, Importação e Exportação de Implantes Médicos, S.A.

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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