Skip to content

Kietosios įtvarinės sistemos

by UAB Ortopedijos klinika 77 variants

Ref UA - Schiene KAB ORTOPEDIJOS KLINIKA "RT1-9 (16341)", Rechts M

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 Number4772165OK0237 Basic UDI-DI 04772165001227UDI-DIDate11 Jun 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  • Withdrawn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
Kietosios įtvarinės sistemos
Model / Reference
UA - Schiene KAB ORTOPEDIJOS KLINIKA "RT1-9 (16341)", Rechts M
Primary DI / UDI-DI
04772165001227
Basic UDI-DI
4772165OK0237
Direct Marketing DI
04772165001227
EMDN Code
Y060609 Wrist (forearm) orthoses
Device Class
Class I
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000004389

Other devices from UAB Ortopedijos klinika

See all devices from UAB Ortopedijos klinika →

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