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Cable Assembly, LiDCO BP Module Transducer Cross Over

by LiDCO Ltd

Ref LI10863Model LI10610

Active European Union

CE MDR

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/MDR Number506011052000Z7T0C01V0049U Basic UDI-DI 05060110521784UDI-DIDate20 Dec 2023RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Cable Assembly, LiDCO BP Module to BD/Argon Transducer
Model / Reference
LI10610, LI10863
Primary DI / UDI-DI
05060110521784
Basic UDI-DI
506011052000Z7T0C01V0049U
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
GB-MF-000008036
Authorised representative
LiDCO Netherlands B.V. NL-AR-000002681

Other devices from LiDCO Ltd

See all devices from LiDCO Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No