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True Lok Evo Kit

by Orthofix GmbH

Ref L.EVO

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 Number426071651ProPack2bNAJG Basic UDI-DI 14260716510641UDI-DIDate21 Aug 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  • Withdrawn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
Class IIb Instrument Set
Model / Reference
L.EVO
Primary DI / UDI-DI
14260716510641
Basic UDI-DI
426071651ProPack2bNAJG
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIb
Medical Purpose
Class IIb Instrument Set

Manufacturer details

EUDAMED SRN
DE-PR-000029903

Other devices from Orthofix GmbH

Properties

Other properties (1)

  • Sterile: No