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Sqa-Vu

by Medical Electronic Systems Europe

Ref EU-VU-FA-01944-00

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5430003332SQAANALIZ1KV Basic UDI-DI 05430003332672UDI-DIDate31 Aug 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  • Withdrawn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

Model / Reference
EU-VU-FA-01944-00
Primary DI / UDI-DI
05430003332672
Basic UDI-DI
5430003332SQAANALIZ1KV
Direct Marketing DI
05430003332672
EMDN Code
W0202050380 Laboratory instruments for microscopic investigations - hardware accessories
Device Class
Class A
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000031278

Other devices from Medical Electronic Systems Europe

See all devices from Medical Electronic Systems Europe →

Properties

  • Professional Testing
  • Surgical Instrument

Other properties (9)

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