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Skiff Ambu

by Acime Frame France EUDAMED

Ref SKIF017Model SKIF-STD-AC

EMDN V08050101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376036546SKIF-STD-ACUX Basic UDI-DIDate6 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
SKIF-STD-AC, SKIF017
Primary DI / UDI-DI
03760365460174
Basic UDI-DI
376036546SKIF-STD-ACUX
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000016067

Other devices from Acime Frame

See all devices from Acime Frame →

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 ad37e9a0-732a-4fa5-aedc-f4fd1e3bd46e 61 fields · synced 22 Oct 2026