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Chair-Stretcher Rs-5

by Ferno Slovakia

Ref 60-4300-001/AW, 60-4300-001Model Ferno Slovakia Stretcher

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8588008129FS_stretcherMY Basic UDI-DI Date1 Apr 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
FS Stretchers
Model / Reference
Ferno Slovakia Stretcher, 60-4300-001/AW, 60-4300-001
Primary DI / UDI-DI
08588008129821, 08588008129814
Basic UDI-DI
8588008129FS_stretcherMY
EMDN Code
V08050103 Emergency and traumatology stretchers
Device Class
Class I
EU 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