Skip to content

Plantar Fasciitis Support

by Ningbo Kangbeien Health Tech. Co., Ltd. 9 variants

Ref DG-519369Model Knee Support;Ankle Support;Plantar Fasciitis Support;Achilles Walking Boot;Compression Sock;Bunion Correction Device;Toe Protector;Foot Arch Support;Heel Cushion

Active European Union

CE MDR

Valid until

No date given

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number698058800LLSUL Basic UDI-DI 06980588001689UDI-DIDate23 Oct 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  • Withdrawn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
Lower Limb Support
Model / reference
Knee Support, Ankle Support, Plantar Fasciitis Support, Achilles Walking Boot, Compression Sock, Bunion Correction Device, Toe Protector, Foot Arch Support, Heel Cushion, DG-519369
Primary DI / UDI-DI
06980588001689
Basic UDI-DI
698058800LLSUL
EMDN code
Y061203 Orthoses, foot (including insoles and inserts)
Device class
Class I
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000059805
Authorised representative
HyperCert Limited B.V. NL-AR-000047746

Other devices from Ningbo Kangbeien Health Tech. Co., Ltd.

See all devices from Ningbo Kangbeien Health Tech. Co., Ltd. →

Properties

Other properties (14)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Reusable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No