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Wire microloop

by Medical Wire & Equipment Co Bath (Ltd) 13 variants

Ref MW194

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number0506025907microloopWP Basic UDI-DI 05060259071539UDI-DIDate22 Jul 2022RegisteredStatusActive

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  • Withdrawn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
Wire microloop
Model / Reference
MW194
Primary DI / UDI-DI
05060259071539
Basic UDI-DI
0506025907microloopWP
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Northern Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000006736
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Medical Wire & Equipment Company (Bath), Ltd.

See all devices from Medical Wire & Equipment Company (Bath), Ltd. →

Properties

Other properties (11)

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