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Evokit Medicazione Assistenza

by Gada Italia S.P.A.

Ref DIALEASYHD02

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 linked in EUDAMED

A group certificate may exist

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 Number805699919DIALEASYHD02DQ Basic UDI-DI 08056999190491UDI-DIDate7 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
DIALEASYHD02
Primary DI / UDI-DI
08056999190491
Basic UDI-DI
805699919DIALEASYHD02DQ
EMDN Code
M04010202, M04010299, M040412
Device Class
Class III
Medical Purpose
medicazione e assistenza nell’accesso venoso

Manufacturer details

EUDAMED SRN
IT-PR-000045332

Other devices from Gada Italia S.P.A.

See all devices from Gada Italia S.P.A. →

Properties

Other properties (1)

  • Sterile: No