Skip to content

HenroCup®

by Henrotek A/S

Ref Ref no. 12878, Ref no. 12889, Ref no. 12883, Ref no. 12899Model Technical aid for disable people

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57048311BU Basic UDI-DI Date7 May 2024RegisteredStatusActive

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  • Withdrawn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

Trade Name
HenroCup®
HenroCup® Lid Standard Lid
Device Name
HenroCup
Model / Reference
Technical aid for disable people, Ref no. 12878, Ref no. 12889, Ref no. 12883, Ref no. 12899
Primary DI / UDI-DI
05704831128784, 05704831128890, 05704831128838, 05704831128999
Basic UDI-DI
57048311BU
Direct Marketing DI
05704831128784
05704831128890
05704831128999
EMDN Code
Y0999 Personal care aids - other
Device Class
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
DK-MF-000029313

Other devices from Henrotek A/S

Properties

  • CMR Substance YesEUDAMEDNoEUDAMED

Other properties (12)

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