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Endoscope Image Processor

by Weyo Surgical Technology Ltd. EUDAMED

Active European Union

Ref wDubhe E20bModel wDubhe E20u、 wDubhe E20p、 wDubhe E20a、 wDubhe E20c、 wDubhe E20g、 wDubhe E20s、 wDubhe E20e、 wDubhe E20b

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697562167Z12020406069A Basic UDI-DIDate12 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Endoscope Image Processor
Model / Reference
wDubhe E20u、 wDubhe E20p、 wDubhe E20a、 wDubhe E20c、 wDubhe E20g、 wDubhe E20s、 wDubhe E20e、 wDubhe E20b, wDubhe E20b
Primary DI / UDI-DI
06975621672346
Basic UDI-DI
697562167Z12020406069A
EMDN Code
Z12020406 Video processors
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000038773
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Weyo Surgical Technology Ltd.

See all devices from Weyo Surgical Technology Ltd. →

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