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Materasso doppia densità 2026

by Storello Ausili SRL

Ref TAUVE3060, SACCONANNAModel Materasso antidecubito doppia densità 30/60, P1506/PCE/LENGA/IGN

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 Number805495381TAUVE3060PF Basic UDI-DI Date30 Apr 2026RegisteredStatusActive

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  • Withdrawn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
Materasso doppia densità 2026
Materasso doppia densità
Sacco Nanna
Model / Reference
Materasso antidecubito doppia densità 30/60, TAUVE3060, P1506/PCE/LENGA/IGN, SACCONANNA
Primary DI / UDI-DI
08054953810881, 80549538100036
Basic UDI-DI
805495381TAUVE3060PF, 805495381TAUVEM5, 805495381CONT_LETTOXJ
Direct Marketing DI
08054953810881
80549538100036
EMDN Code
V080702, Y99, M030599
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000045673

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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