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Evokit Prelievo

by Gada Italia S.P.A. EUDAMED

Active European Union

Ref PRELBG001

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805699919PRELBG0014A Basic UDI-DIDate26 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Model / Reference
PRELBG001
Primary DI / UDI-DI
08056999190101
Basic UDI-DI
805699919PRELBG0014A
EMDN Code
A018099,A020102010201,A020102020102,A02010701,A07050202,A0706,D02010102,M0202010101,T020199
Device Class
Class III
Medical Purpose
Medicazione e assistenza

Manufacturer details

EUDAMED SRN
IT-PR-000045332

Other devices from Gada Italia S.P.A.

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Properties

Other properties (1)

  • Sterile: No