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Adult diaper

by Kimlead Hygiene Products(Hebei) Co., Ltd. 24 variants

Ref XLModel 650*800， 750*900， 800*900， 1000*1200， M， L， XL ，XXL

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 Number697535962ZNK001WE Basic UDI-DI 06975359620152UDI-DIDate4 Sep 2023RegisteredStatusActive

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  • Withdrawn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
Adult diaper
Model / Reference
650*800， 750*900， 800*900， 1000*1200， M， L， XL ，XXL, XL
Primary DI / UDI-DI
06975359620152
Basic UDI-DI
697535962ZNK001WE
EMDN Code
Y0999 Personal care aids - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000025989
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Kimlead Hygiene Products(Hebei) Co., Ltd.

See all devices from Kimlead Hygiene Products(Hebei) Co., Ltd. →

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