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Veos

by CANFIELD SCIENTIFIC Inc United States EUDAMED

Ref 51550 EMDN Z12040108

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number008600106181VEOS8K Basic UDI-DIDate25 Mar 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  • Withdrawn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 · synced 22 Oct 2026

Model / Reference
51550
Primary DI / UDI-DI
00860010618134
Basic UDI-DI
008600106181VEOS8K
EMDN Code
Z12040108 Dermatoscopes
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
US-MF-000042029
Authorised representative
CANFIELD SCIENTIFIC SRL IT-AR-000040560

Other devices from CANFIELD SCIENTIFIC Inc

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED b17d0c17-66c3-4030-ab5c-cd72fc4d8dd2 61 fields · synced 22 Oct 2026