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Crutch

by Shenzhen Aonuo Medical Technology Co., Ltd. 7 variants

Model AN-501,AN-502,AN-503,AN-504,AN-505,AN-506,AN-507(or customized)

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 Number697539269ANCRSD Basic UDI-DI 06975392695049UDI-DIDate27 Dec 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  • Withdrawn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
Crutch
Model / Reference
AN-501, AN-502, AN-503, AN-504, AN-505, AN-506, AN-507(or customized)
Primary DI / UDI-DI
06975392695049
Basic UDI-DI
697539269ANCRSD
EMDN Code
Y12030603 Crutches with under-axle support
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000038823
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shenzhen Aonuo Medical Technology Co., Ltd.

See all devices from Shenzhen Aonuo Medical Technology 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