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Guide wire smooth tip Ø 2 mm x L. 600 mm

by LSM-MED S.r.l.

Ref 9087.30.003Model GUIDE WIRES

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 Number8033051STR07010005BF Basic UDI-DI 08033051098568UDI-DIDate27 May 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  • Withdrawn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

Model / Reference
GUIDE WIRES, 9087.30.003
Primary DI / UDI-DI
08033051098568
Basic UDI-DI
8033051STR07010005BF
EMDN Code
L0922 Orthopaedic surgery guides, reusable
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
SM-MF-000033593
Authorised representative
Overmed srl IT-AR-000021275

Other devices from LSM-MED S.r.l.

See all devices from LSM-MED S.r.l. →

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