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S24 Transfer

by Howard Wright Limited EUDAMED

Active European Union

Ref S24+4111+115Model S24 Stretcher

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number942904017343S24Q9 Basic UDI-DIDate4 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
S24 Stretcher
Model / Reference
S24 Stretcher, S24+4111+115
Primary DI / UDI-DI
09344090018448
Basic UDI-DI
942904017343S24Q9
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NZ-MF-000009802
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Howard Wright Limited

See all devices from Howard Wright Limited →

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