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Dakota Max Double

by CICHOSZ Spółka Komandytowa EUDAMED

Withdrawn No longer placed on the EU market

Ref MDMAXDModel DAKOTA MAX DOUBLE

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5905215700DAKOTAMAXDOURR Basic UDI-DIDate7 Oct 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Materac medyczny DAKOTA MAX DOUBLE
Model / Reference
DAKOTA MAX DOUBLE, MDMAXD
Primary DI / UDI-DI
05905215700705
Basic UDI-DI
5905215700DAKOTAMAXDOURR
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I

Manufacturer details

EUDAMED SRN
PL-MF-000029162

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