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17-6 Ferno Stretcher

by Ferno Slovakia EUDAMED

Withdrawn No longer placed on the EU market

Ref 60-0118-002Model Ferno Stretcher

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8588008129Ferno17StretcPE Basic UDI-DIDate6 Apr 2022RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Ferno Stretcher
Model / Reference
Ferno Stretcher, 60-0118-002
Primary DI / UDI-DI
08588008129791
Basic UDI-DI
8588008129Ferno17StretcPE
EMDN Code
V08050103 Emergency and traumatology stretchers
Device Class
Class I
Market of Registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000001474

Other devices from Ferno Slovakia

See all devices from Ferno Slovakia →

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