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Kit Dynamisation Tl-Hex Et Truelok

by Orthofix France SAS

Ref V.DYNA

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376034736ProPack1rNAXC Basic UDI-DI 13760347360222UDI-DIDate16 Mar 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  • Withdrawn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
VALISE OPERATOIRE Classe Ir
Model / Reference
V.DYNA
Primary DI / UDI-DI
13760347360222
Basic UDI-DI
376034736ProPack1rNAXC
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
VALISE OPÉRATOIRE ORTHOPÉDIE

Manufacturer details

EUDAMED SRN
FR-PR-000009701

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Category: Ophthalmic surgical procedure kit, non-medicated, single-use

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Properties

Other properties (1)

  • Sterile: No