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Reusable Water Trap

by VADI Medical Technology Co., Ltd. 8 variants

Ref G-313003-2-1-ENModel G-313003-2-1

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04719875345777 Basic UDI-DI 04719875345777UDI-DIDate5 Jun 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
G-313003-2-1, G-313003-2-1-EN
Primary DI / UDI-DI
04719875345777
Basic UDI-DI
B-04719875345777
EMDN Code
R028003 Respiratory circuits water traps
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TW-MF-000022930
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Other devices from VADI Medical Technology Co., Ltd.

See all devices from VADI Medical Technology Co., Ltd. →

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