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Upgrade Kit Victus SW3.3 SP04

by Technolas Perfect Vision GmbH

Ref 14678TVP

Active European Union

CE MDD

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/MDD NumberB-14678TPVME Basic UDI-DI D-14678TPVMEUDI-DIDate22 Jun 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Upgrade Kit Victus SW3.3 SP04
Model / Reference
14678TVP
Primary DI / UDI-DI
D-14678TPVME
Basic UDI-DI
B-14678TPVME
EMDN Code
Z12011006 Diode–pumped solid–state (dpss) surgical laser
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
DE-MF-000007094

Other devices from Technolas Perfect Vision GmbH

See all devices from Technolas Perfect Vision GmbH →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No