Skip to content

Polysite 2000 Port Sil 6, 5F C/Kit Cvc

by Vygon Italia SRL

Ref A2007ISP05

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 Number805960273D01A2000ISP-5S5B Basic UDI-DI 08059602732774UDI-DIDate22 Jul 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  • Withdrawn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
A2007ISP05
Primary DI / UDI-DI
08059602732774
Basic UDI-DI
805960273D01A2000ISP-5S5B
EMDN Code
C01020401 Subcutaneous implantable venous access port systems, single-chamber
Device Class
Class III
Medical Purpose
"Kit con CVC in silicone a camera impiantabile e accessori per l'impianto e la verifica del posizionamento con tecnica ECG"

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