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Prosthetic Screw HG F.A.S.

by New Ancorvis SRL EUDAMED

Active European Union

Ref HGVTXOS35Model Viti Protesiche

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8053876-01-012N6 Basic UDI-DIDate23 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Viti Protesiche
Model / Reference
Viti Protesiche, HGVTXOS35
Primary DI / UDI-DI
08053876085567
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008879

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