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Underpad

by Kourich Industry Limited 9 variants

Ref 60*40cmModel 60*40cm, 60*60cm, 60*90cm, 33*45cm, 60*45cm, 75*75cm, 76*90cm, 90*90cm, 100*225cm

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 Number698030962Underpad22 Basic UDI-DI 06980309620144UDI-DIDate20 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Underpad
Model / Reference
60*40cm, 60*60cm, 60*90cm, 33*45cm, 60*45cm, 75*75cm, 76*90cm, 90*90cm, 100*225cm
Primary DI / UDI-DI
06980309620144
Basic UDI-DI
698030962Underpad22
EMDN Code
T04010299 Absorbent underpads - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000057251
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Kourich Industry Limited

See all devices from Kourich Industry Limited →

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