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Eksterni fiksator- šipka

by Narcissus doo 5 variants

Ref NA.F8.250

Active European Union

CE MDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08605029615840 Basic UDI-DI 08605029615840UDI-DIDate31 May 2022RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
External fixator- Bar
Model / Reference
NA.F8.250
Primary DI / UDI-DI
08605029615840
Basic UDI-DI
B-08605029615840
EMDN Code
P09120499 External bone fixation systems - other
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
RS-MF-000022423
Authorised representative
Narcmed Kft. HU-AR-000020491

Other devices from Narcissus doo

See all devices from Narcissus doo →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No