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Leadercath C/Trasdutt. Disposet Edwards

by Vygon Italia SRL

Ref A115.09010B

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 Number805960273D01A115-10BBF Basic UDI-DI 08059602733320UDI-DIDate14 Sep 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  • Withdrawn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
A115.09010B
Primary DI / UDI-DI
08059602733320
Basic UDI-DI
805960273D01A115-10BBF
EMDN Code
C010301 Radial cannulas
Device Class
Class IIa
Medical Purpose
Kit con catetere arterioso e set per il monitoraggio della pressione arteriosa

Manufacturer details

EUDAMED SRN
IT-PR-000012626

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Properties

Other properties (1)

  • Sterile: No