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Stabilizator stawu kolanowego neoprenowy

by Private Enterprise Toros-Group

Ref Type 511-3Model Type 511

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 Number4820114085115Y Basic UDI-DI 04820114083340UDI-DIDate2 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Neoprene Knee Bandage with 2 ribs
Model / Reference
Type 511, Type 511-3
Primary DI / UDI-DI
04820114083340
Basic UDI-DI
4820114085115Y
Direct Marketing DI
04820114083340
EMDN Code
Y061209 Knee orthoses
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
UA-MF-000051136
Authorised representative
Medtex Sp. z o.o. PL-AR-000009252

Other devices from Private Enterprise Toros-Group

See all devices from Private Enterprise Toros-Group →

Properties

  • Reprocessed

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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