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QwikCheck Beads

by MES Medical Electronic Systems LTD

Ref A-CA-01659-00

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number7290016650BEADS1V7 Basic UDI-DI 07290016650396UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
QwikCheck Beads
Model / Reference
A-CA-01659-00
Primary DI / UDI-DI
07290016650396
Basic UDI-DI
7290016650BEADS1V7
Direct Marketing DI
07290016650396
EMDN Code
W05039080 Devices for samples analyses - other accessories
Device Class
Class B
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IL-MF-000034514
Authorised representative
Arazy Group GmbH DE-AR-000007685

Other devices from MES Medical Electronic Systems LTD

See all devices from MES Medical Electronic Systems LTD →

Properties

  • Professional Testing

Other properties (10)

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