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Coventry: Triple lumen extension set: 2 x anti-siphon, 1 x high-flow back check valve (17cm/7")

by Mediplus Ltd

Ref 6510

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-05055140702241 Basic UDI-DI 05055140702241UDI-DIDate17 Aug 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Coventry: Triple lumen extension set: 2 x anti-siphon, 1 x high-flow back check valve (17cm/7")
Model / Reference
6510
Primary DI / UDI-DI
05055140702241
Basic UDI-DI
B-05055140702241
EMDN Code
A070103 Infusion tubing adapters and connectors
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000031075
Authorised representative
Mediplus GmbH DE-AR-000030648

Other devices from Mediplus Ltd.

See all devices from Mediplus Ltd. →

Properties

  • Sterile
  • Administering Medicine

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No