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Forearm Crutch with Adjustable Handle for Children - Blue

by Μοναδα Βιομηχανικων Ιατρικων Αεριων Κρητης (Μοβιακ Α.ε)

Ref 0813172

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number521300690walkingaids10N3 Basic UDI-DI 05213016044066UDI-DIDate20 Mar 2025RegisteredStatusActive

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  • Withdrawn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
Walking Aid
Model / Reference
0813172
Primary DI / UDI-DI
05213016044066
Basic UDI-DI
521300690walkingaids10N3
Direct Marketing DI
05213016044066
EMDN Code
Y12030601 Elbow crutches
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000016256

Other devices from Μοναδα Βιομηχανικων Ιατρικων Αεριων Κρητης (Μοβιακ Α.ε)

See all devices from Μοναδα Βιομηχανικων Ιατρικων Αεριων Κρητης (Μοβιακ Α.ε) →

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