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Περικνημιδα Ελαστικη

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

Ref 1807

Περικνημιδα Ελαστικη (1807) is a Class I device made by Ανατομικ Χελπ Ανωνυμη Εταιρια Εμποριας Και Κατασκευης Ορθοπεδικων Ειδων Α.Ε., registered in EUDAMED on 17 Dec 2021 (Basic UDI-DI 52049141807LQ), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number52049141807LQ Basic UDI-DI Date17 Dec 2021RegisteredStatusActive

Official records

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  • Withdrawn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
Περικνημιδα Ελαστικη / Thigh Support
Model / reference
1807
Primary DI / UDI-DI
05204914343511, 05204914343498, 05204914343528, 05204914343481, 05204914343474, 05204914343504
Basic UDI-DI
52049141807LQ
EMDN code
Y06120601 Passive ankle-foot orthoses
Device class
Class I
EU registration type
Standard device
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000015975

Similar devices in this category

Other devices filed under PASSIVE ANKLE-FOOT ORTHOSES.

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Properties

  • Contains latex
Other properties (13, all answered No)