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Transtube

by Medical Wire & Equipment Co Bath (Ltd) 4 variants

Ref MW176

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060259070150 Basic UDI-DI 05060259070150UDI-DIDate21 Nov 2022RegisteredStatusActive

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  • Withdrawn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

Device Name
Transtube
Model / Reference
MW176
Primary DI / UDI-DI
05060259070150
Basic UDI-DI
B-05060259070150
EMDN Code
A1102 Sample collection swabs with transport medium
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

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

Related devices

Category: General-purpose absorbent tip applicator/swab, single-use

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

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

Properties

  • Sterile

Other properties (10)

  • 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