Skip to content

Minimid Leaderflex Pack 02 22g 8cm

by Vygon Italia SRL

Ref A1212.0802

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805960273D01A1212-24R Basic UDI-DI 08059602731197UDI-DIDate4 Aug 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  • Withdrawn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

Device Name
Minimid Leaderflex Pack 02
Model / Reference
A1212.0802
Primary DI / UDI-DI
08059602731197
Basic UDI-DI
805960273D01A1212-24R
EMDN Code
C010102 Peripheral i.v. catheter systems
Device Class
Class IIa
Medical Purpose
Set per cateterismo venoso periferico di tipo Midline con sistema di fissaggio sutureless e accesso needle-free

Manufacturer details

EUDAMED SRN
IT-PR-000012626

Other devices from Vygon Italia SRL

See all devices from Vygon Italia SRL →

Properties

Other properties (1)

  • Sterile: No