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Ζωνη Ακινητοποιησης Ωμου

by Ανατομικ Χελπ Ανωνυμη Εταιρια Εμποριας Και Κατασκευης Ορθοπεδικων Ειδων Α.Ε.

Ref 0320

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 Number52049140320KG Basic UDI-DI Date17 Dec 2021RegisteredStatusActive

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  • Withdrawn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
Ζωνη Ακινητοποιησης Ωμου / Shoulder Immobilizator with Strap
Model / Reference
0320
Primary DI / UDI-DI
05204914324282, 05204914371569, 05204914324275
Basic UDI-DI
52049140320KG
EMDN Code
Y210924 Arm supports
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000015975

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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