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V-VR Tip 3

by Viora Ltd

Ref VTL48013Model V-VR Tip 3 units

V-VR Tip 3 (VTL48013) is a Class IIb device made by Viora Ltd., registered in EUDAMED on 24 Jun 2026 (Basic UDI-DI B-07290016746518), active as of 22 Oct 2026.

Active European Union

CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290016746518 Basic UDI-DI 07290016746518UDI-DIDate24 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
V-VR Tip 3 units
Model / reference
V-VR Tip 3 units, VTL48013
Primary DI / UDI-DI
07290016746518
Basic UDI-DI
B-07290016746518
EMDN code
V9099 Various devices not included in other classes - other
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000039108
Authorised representative
Obelis s.a. BE-AR-000000106

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Properties

  • Supplied sterile
Other properties (11, all answered No)