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Magnifico

by MATERASSO Slovakia, s.r.o. 3 variants

Ref 8586025258784, 8586025258982, 8586025258951, 8586025258890, 8586025259002, 8586025258975, 8586025259033, 8586025258937, 8586025258876, 8586025258999, 8586025259026, 8586025258883, 8586025258913Model Penový matrac

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number858602525MatracpenoveP2 Basic UDI-DI Date16 Aug 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Magnifico
Magnifico Polargel
Device Name
Matrac
Model / Reference
Penový matrac, 8586025258784, 8586025258982, 8586025258951, 8586025258890, 8586025259002, 8586025258975, 8586025259033, 8586025258937, 8586025258876, 8586025258999, 8586025259026, 8586025258883, 8586025258913
Primary DI / UDI-DI
08586025258784, 08586025258982, 08586025258951, 08586025258890, 08586025259002, 08586025258975, 08586025259033, 08586025258937, 08586025258876, 08586025258999, 08586025259026, 08586025258883, 08586025258913
Basic UDI-DI
858602525MatracpenoveP2
Direct Marketing DI
08586025258784
08586025258982
08586025258951
08586025258890
08586025259002
08586025258975
08586025259033
08586025258937
08586025258876
08586025258999
08586025259026
08586025258883
08586025258913
EMDN Code
V080702 Non active anti-decubitus medical mattresses
Device Class
Class I
EU 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