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F2_TRL

by Ferno Slovakia EUDAMED

Active European Union

Ref 60-0321-001_BLKModel F2 Product Family

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number858602790F2PRODUCTFAMILJV Basic UDI-DIDate14 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
F2 series
Model / Reference
F2 Product Family, 60-0321-001_BLK
Primary DI / UDI-DI
08586027902364
Basic UDI-DI
858602790F2PRODUCTFAMILJV
Direct Marketing DI
08586027902364
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

Show 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