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Evokit Fixation Midline

by Gada Italia S.P.A. EUDAMED

Active European Union

Ref FIXAPGP01

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805699919FIXAPGP0172 Basic UDI-DIDate14 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
FIXAPGP01
Primary DI / UDI-DI
08056999190446
Basic UDI-DI
805699919FIXAPGP0172
EMDN Code
M04010101,M04010299
Device Class
Class I
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