Skip to content

Sensilind Complete Care Slip super 1 S 1x

by Ontex BV

Ref EREF13.11.1Model Heavy Inco

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5414874HeavyIncoG5 Basic UDI-DI 05414874022481UDI-DIDate30 Apr 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  • Withdrawn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

Device Name
Heavy Incontinence Devices
Model / Reference
Heavy Inco, EREF13.11.1
Primary DI / UDI-DI
05414874022481
Basic UDI-DI
5414874HeavyIncoG5
EMDN Code
T04010103 Incontinence nappies with integrated fixing system
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
BE-MF-000003544

Other devices from Ontex BV

See all devices from Ontex BV →

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