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Medilon Braces

by Medilon Braces 8 variants

Ref MB7004-2Model Medilon Genustab Kniebrace, Medilon Patellabrace

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8720865045KNB-STABZH Basic UDI-DI Date29 May 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  • Withdrawn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

Model / Reference
Medilon Genustab Kniebrace, MB7004-2, Medilon Patellabrace
Primary DI / UDI-DI
08720865045443, 08720865045160
Basic UDI-DI
8720865045KNB-STABZH, 8720865045PTB-STAB7R
EMDN Code
Y061209 Knee orthoses
Device Class
Class I
EU market of registration
Poland
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000047759

Other devices from Medilon Braces

See all devices from Medilon Braces →

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