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ORIGIN® KNEE-PLAN® Guides

by Symbios Orthopédie S.A. 2 variants

Ref 9005 0000Model KNEE-PLAN Guides Set

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number763001361AQI02203002XXXCY Basic UDI-DI 07630013669425UDI-DIDate9 Jun 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  • Withdrawn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

Model / Reference
KNEE-PLAN Guides Set, 9005 0000
Primary DI / UDI-DI
07630013669425
Basic UDI-DI
763001361AQI02203002XXXCY
EMDN Code
P091399 Orthopaedic implant instruments, single-use - other
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000020168
Authorised representative
Symbios France SAS FR-AR-000017731

Other devices from Symbios Orthopédie S.A.

See all devices from Symbios Orthopédie S.A. →

Properties

  • Sterile

Other properties (12)

  • 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