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Universal fixation splint systems

by UAB Ortopedijos klinika 41 variants

Ref Hand splint ORTOPEDIJOS KLINIKA "UFS-08LS"

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 Number4772165OK0339 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Universal fixation splint systems
Model / Reference
Hand splint ORTOPEDIJOS KLINIKA "UFS-08LS"
Primary DI / UDI-DI
04772165001890
Basic UDI-DI
4772165OK0339
Direct Marketing DI
04772165001890
EMDN Code
Y060606 Hand orthoses
Device Class
Class I
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