Skip to content

Volumed Set

by Phoenix S.R.L. 146 variants

Ref 1002550321Model Dispositivi per Infusione ed Aspirazione

Active European Union

CE MDR

Valid until

13 Feb 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ICIM S.P.A.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805274795INFNN Basic UDI-DI 08052747953394UDI-DIDate15 May 2024RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030019-04 Active

    Quality management system EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    23 Jul 2026
    Expires
    13 Feb 2028

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Dispositivi per Infusione ed Aspirazione, 1002550321
Primary DI / UDI-DI
08052747953394
Basic UDI-DI
805274795INFNN
EMDN Code
A03010105 Infusion pump controllers
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000023426

Other devices from Phoenix S.R.L.

See all devices from Phoenix S.R.L. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No