Skip to content

Relexta-Spreizwindel T1

by AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte 2 variants

Ref 600-12-T1Model Relexta-Abspreizhose Typ I

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-110963521441 Basic UDI-DI 110963521441UDI-DIDate26 Nov 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
RELEXTA-Abspreizhose T1-Gr.0
Model / Reference
Relexta-Abspreizhose Typ I, 600-12-T1
Primary DI / UDI-DI
110963521441
Basic UDI-DI
B-110963521441
EMDN Code
Y061215 Hip orthoses (including abduction orthoses)
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008562

Other devices from AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte

See all devices from AIDAMED - Produktion & Vertrieb medizinische Produkte & Geräte →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No