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Kit medicazione dialisi mensile

by D.R.M. S.R.L.

Ref PD-MED-A0Model Kit di medicazione

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805959152KITAM1MT Basic UDI-DI 08059591524770UDI-DIDate7 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  • Withdrawn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

Model / Reference
Kit di medicazione, PD-MED-A0
Primary DI / UDI-DI
08059591524770
Basic UDI-DI
805959152KITAM1MT
EMDN Code
T0203 Dressing and assistance kits
Device Class
Class I
Medical Purpose
Kit per medicazione e assistenza

Manufacturer details

EUDAMED SRN
IT-PR-000031790

From the manufacturer

Manufacturer's product page: Kit per dialisi e medicazione generica

Other devices from D.R.M. S.R.L.

See all devices from D.R.M. S.R.L. →

Properties

Other properties (1)

  • Sterile: No