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ReLink IV

by Interlinked AB

Ref ReLink IV 1

Active European Union

CE MDR

Valid until

24 Feb 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV NORD CERT GmbH

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/MDR Number44910261701 Date13 Oct 2026IssuedStatusActive expires 24 Feb 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 44910261701 Active

    Quality assurance EU MDR

    Certifier
    TÜV NORD CERT GmbH 0044
    Issued
    13 Oct 2026
    Expires
    24 Feb 2030

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ReLink IV
Model / Reference
ReLink IV 1
Primary DI / UDI-DI
07350128050061
Basic UDI-DI
735012805ReLinkAdvTS
EMDN Code
A070103 Infusion tubing adapters and connectors
Device Class
Class IIa
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000040455

Other devices from Interlinked AB

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