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Termopur comfort

by MATERASSO Slovakia, s.r.o. 21 variants

Ref 8586020354344, 8586025258647, 8586020352777, 8586020354177, 8586020352647, 8586020354238, 8586020352753, 8586020352593, 8586020352630, 8586025258630, 8586020354214, 8586020354245, 8586020352708, 8586020352654, 8586025258609, 8586020354351, 8586020354320, 8586020354191, 8586025258623, 8586020354160, 8586020352586, 8586020352739, 8586025258654, 8586020352678, 8586025258616Model 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  • Withdrawn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

Device Name
Matrac
Model / Reference
Penový matrac, 8586020354344, 8586025258647, 8586020352777, 8586020354177, 8586020352647, 8586020354238, 8586020352753, 8586020352593, 8586020352630, 8586025258630, 8586020354214, 8586020354245, 8586020352708, 8586020352654, 8586025258609, 8586020354351, 8586020354320, 8586020354191, 8586025258623, 8586020354160, 8586020352586, 8586020352739, 8586025258654, 8586020352678, 8586025258616
Primary DI / UDI-DI
08586020354344, 08586025258647, 08586020352777, 08586020354177, 08586020352647, 08586020354238, 08586020352753, 08586020352593, 08586020352630, 08586025258630, 08586020354214, 08586020354245, 08586020352708, 08586020352654, 08586025258609, 08586020354351, 08586020354320, 08586020354191, 08586025258623, 08586020354160, 08586020352586, 08586020352739, 08586025258654, 08586020352678, 08586025258616
Basic UDI-DI
858602525MatracpenoveP2
Direct Marketing DI
08586020354344
08586025258647
08586020352777
08586020354177
08586020352647
08586020354238
08586020352753
08586020352593
08586020352630
08586025258630
08586020354214
08586020354245
08586020352708
08586020352654
08586025258609
08586020354351
08586020354320
08586020354191
08586025258623
08586020354160
08586020352586
08586020352739
08586025258654
08586020352678
08586025258616
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

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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