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Artemis II

by Drive Medical Limited United Kingdom EUDAMED

Ref ARTEMIS/2/CUSH/18Model Artemis II dynamic cushion (surface only) EMDN V08030101

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50557857DPC007FJ Basic UDI-DIDate5 Apr 2023RegisteredStatusActive

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  • Withdrawn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 · synced 24 Oct 2026

Device Name
Artemis II dynamic cushion
Model / Reference
Artemis II dynamic cushion (surface only), ARTEMIS/2/CUSH/18
Primary DI / UDI-DI
05055785718485
Basic UDI-DI
50557857DPC007FJ
EMDN Code
V08030101 Active anti-decubitus medical cushions
Device Class
Class I
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000012818
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Drive Medical Limited

See all devices from Drive Medical Limited →

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 16cfd049-6999-47f1-b3a6-de0f6fd9016c 61 fields · synced 24 Oct 2026