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Kit Ablation Fitbone

by Orthofix France SAS

Ref V.ABLFB

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376034736ProPack2aNAUW Basic UDI-DI 13760347360383UDI-DIDate9 Dec 2025RegisteredStatusActive

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  • Withdrawn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
VALISE OPERATOIRE Classe IIa
Model / Reference
V.ABLFB
Primary DI / UDI-DI
13760347360383
Basic UDI-DI
376034736ProPack2aNAUW
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Medical Purpose
VALISE OPERATOIRE ORTHOPEDIE

Manufacturer details

EUDAMED SRN
FR-PR-000009701

Related devices

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

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Properties

Other properties (1)

  • Sterile: No