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Italfix-Mutanda Di Fissaggio Elasticizzata Riutilizzabile Taglia Xl

by I.T.A.L. S.r.l.

Ref ITMF-XLModel ITALFIX-MUTANDA DI FISSAGGIO ELASTICIZZATA RIUTILIZZABILE TAGLIA S

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 Number8050628381755ZW Basic UDI-DI 08050628381755UDI-DIDate9 May 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  • Withdrawn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
Italfix-Mutanda Di Fissaggio Elasticizzata Riutilizzabile-Itmf-S
Model / Reference
ITALFIX-MUTANDA DI FISSAGGIO ELASTICIZZATA RIUTILIZZABILE TAGLIA S, ITMF-XL
Primary DI / UDI-DI
08050628381755
Basic UDI-DI
8050628381755ZW
Direct Marketing DI
08050628381755
EMDN Code
T0499 Incontinence devices - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000039832

Other devices from I.T.A.L. S.r.l.

See all devices from I.T.A.L. S.r.l. →

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