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Versa

by PENTAX-Aohua Medical Technologies Co., Ltd. EUDAMED

Active European Union

Ref EPK-V1500c

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number697227211EPKPQ Basic UDI-DIDate19 May 2026RegisteredStatusActive
European UnionCE/MDR Number697227211EPKPQ Basic UDI-DIDate19 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

No EU certificate is linked to this device in EUDAMED.

Specification

EUDAMED

Device Name
PENTAX Medical Video Processor
Model / Reference
EPK-V1500c
Primary DI / UDI-DI
06972272110050
Basic UDI-DI
697227211EPKPQ, B-06972272110050
Direct Marketing DI
06972272110050
EMDN Code
Z12020406 Video processors
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000005686
Authorised representative
PENTAX Europe GmbH DE-AR-000000006

Other devices from PENTAX-Aohua Medical Technologies Co., Ltd.

  • Versa

    Class IIa

  • Versa

    Class I

  • Versa

    Class IIa

  • Versa

    Class IIa

  • Versa

    Class IIa

Properties

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