Skip to content

bunion corrector

by Shijiazhuang aofeite imp&exp co., ltd 16 variants

Ref ZSHB

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 Number69537519BUC01RJ Basic UDI-DI Date25 Nov 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  • Withdrawn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
bunion corrector
Model / Reference
ZSHB
Primary DI / UDI-DI
06953780304377, 06953751914765
Basic UDI-DI
69537519BUC01RJ, 69537519BUNION2C
EMDN Code
Y061299, Y061203
Device Class
Class I
EU market of registration
Germany
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000011825
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shijiazhuang aofeite imp&exp co., ltd

See all devices from Shijiazhuang aofeite imp&exp 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