Skip to content

Rampa 5 Rubin. C/PROL.100CM/6BIONECTOR

by Vygon Italia SRL

Ref A5828.1501

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 Number805960273D01A5828-19J Basic UDI-DI 08059602733443UDI-DIDate21 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  • Withdrawn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
A5828.1501
Primary DI / UDI-DI
08059602733443
Basic UDI-DI
805960273D01A5828-19J
EMDN Code
A0702 Ramps
Device Class
Class IIa
Medical Purpose
Accessori per linea infusionale I.V.

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