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EpiShuttle Patient Isolation Unit

by Epiguard AS Norway EUDAMED

Ref 33868Model AS01

EMDN V08050104

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number709005613AS0159 Basic UDI-DIDate7 Mar 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
EpiShuttle
Model / Reference
AS01, 33868
Primary DI / UDI-DI
07090056130014
Basic UDI-DI
709005613AS0159
Direct Marketing DI
07090056130014
EMDN Code
V08050104 Bio-containment stretchers
Device Class
Class I
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
NO-MF-000018011

Other devices from EpiGuard AS

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 8e2028cc-8c3a-4852-9995-9553f73b1d6f 61 fields · synced 24 Oct 2026