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Monaco Dream

by MATERASSO Slovakia, s.r.o. EUDAMED

Active European Union

Ref 8586025256483Model Penový matrac

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number858602525MatracpenoveP2 Basic UDI-DIDate16 Aug 2025RegisteredStatusActive

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  • Withdrawn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
Matrac
Model / Reference
Penový matrac, 8586025256483
Primary DI / UDI-DI
08586025256483
Basic UDI-DI
858602525MatracpenoveP2
Direct Marketing DI
08586025256483
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I
Market of Registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000044986

Other devices from MATERASSO Slovakia, s.r.o.

See all devices from MATERASSO Slovakia, s.r.o. →

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