Skip to content

Elastic Ankle M

by Miracle Medical Industries

Ref 6222012025268

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6222012025268MK Basic UDI-DI 06222012025268UDI-DIDate31 Jan 2023RegisteredStatusActive

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  • Withdrawn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
Elastic Ankle M
Model / Reference
6222012025268
Primary DI / UDI-DI
06222012025268
Basic UDI-DI
6222012025268MK
EMDN Code
Y061218 Hip-knee-ankle-foot orthoses
Device Class
Class I
EU market of registration
Northern Ireland

Manufacturer details

EUDAMED SRN
EG-MF-000032514
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Miracle Medical Industries

See all devices from Miracle Medical Industries →

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