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LiDCO Injectate Kit

by LiDCO Ltd 2 variants

Ref CM 50-EUW-01

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506011052000Z7T5C01V003CR Basic UDI-DI 05060110521791UDI-DIDate14 Dec 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
CM 50-EUW-01
Primary DI / UDI-DI
05060110521791
Basic UDI-DI
506011052000Z7T5C01V003CR
EMDN Code
Z12050785 Instruments for cardiological polygraphy - consumables
Device Class
Class IIa
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

  • Sterile
  • Administering Medicine

Other properties (11)

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