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Crutch

by Shenzhen Aonuo Medical Technology Co., Ltd. EUDAMED

Active European Union

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

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697539269ANCRSD Basic UDI-DIDate27 Dec 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

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
06975392695070
Basic UDI-DI
697539269ANCRSD
EMDN Code
Y120318 Quadripods
Device Class
Class I
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