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Multicath Basic Pack 5l 9, 5F 30cm

by Vygon Italia SRL

Ref A159.35203

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805960273D01A157-3W3 Basic UDI-DI 08059602733962UDI-DIDate30 Jun 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  • Withdrawn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
Multicath Basic Pack 2l 7,5F 30cm
Model / Reference
A159.35203
Primary DI / UDI-DI
08059602733962
Basic UDI-DI
805960273D01A157-3W3
EMDN Code
C01020203 Central venous multi-lumen (>2) catheters, non-tunneled
Device Class
Class IIa
Medical Purpose
Set per con CVC multilume e accessori per il posizionamento

Manufacturer details

EUDAMED SRN
IT-PR-000012626

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Properties

Other properties (1)

  • Sterile: No