Skip to content

Lugano Top

by MATERASSO Slovakia, s.r.o. EUDAMED

Active European Union

Ref 8586025257978, 8586025257985, 8586025257992, 8586025257961, 8586025257954Model HR matrac

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number858602525MatracHRP3 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  • Withdrawn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
HR matrac, 8586025257978, 8586025257985, 8586025257992, 8586025257961, 8586025257954
Primary DI / UDI-DI
08586025257978, 08586025257985, 08586025257992, 08586025257961, 08586025257954
Basic UDI-DI
858602525MatracHRP3
Direct Marketing DI
08586025257978
08586025257985
08586025257992
08586025257961
08586025257954
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