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5 L Eau Demineralisee / Recipient En Plastique

by Yvsolab NV

Ref SL.WGD0.05/375Model 5 L DEMI-WATER

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/IVDR Number540700797SLWGD005YR Basic UDI-DI 05407007970308UDI-DIDate5 Feb 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
5 L Demi-Water
Model / Reference
5 L DEMI-WATER, SL.WGD0.05/375
Primary DI / UDI-DI
05407007970308
Basic UDI-DI
540700797SLWGD005YR
EMDN Code
W01030799 Histology / cytology reagents - other
Device Class
Class A
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000024599

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Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No