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ORIGIN® PS Tibia Modular Set

by Symbios Orthopédie S.A.

Ref 9005 0013Model ORIGIN® Tibia Set

ORIGIN® PS Tibia Modular Set (9005 0013) is a Class IIa device made by Symbios Orthopédie S.A., registered in EUDAMED on 30 Jun 2026 (Basic UDI-DI 763001361AQL02233002XXXJ8), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number763001361AQL02233002XXXJ8 Basic UDI-DI Date30 Jun 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 763001361AQL02233002XXXJ8 — open Devices and search for it

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
ORIGIN® Tibia Set, 9005 0013
Primary DI / UDI-DI
07630013669463, 07630013660729
Basic UDI-DI
763001361AQL02233002XXXJ8, 763001360AQL02233002XXXGR
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
France

Manufacturer details

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

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

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Properties

  • Supplied sterile
Other properties (13, all answered No)