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Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA KT3-8

by UAB Ortopedijos klinika

Ref Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA "KT3-8"Model Wrist with thumb SP ORTOPEDIJOS KLINIKA "RT1-8-2-1"

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 Number4772165OK0135 Basic UDI-DI 04772165000404UDI-DIDate25 May 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  • Withdrawn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

Model / Reference
Wrist with thumb SP ORTOPEDIJOS KLINIKA "RT1-8-2-1", Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA "KT3-8"
Primary DI / UDI-DI
04772165000404
Basic UDI-DI
4772165OK0135
Direct Marketing DI
04772165000404
EMDN Code
Y061209 Knee orthoses
Device Class
Class I
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000004389

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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