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RACCORDO ARMATO ALTA PRESSIONE RA/LLF cm 120(TUBO 1200 psi)

by Med Italia Biomedica S.R.L

Ref 3233871Model DISPOSITIVI E ACCESSORI PER INFUSIONE E/O MONITORAGGIO

Active European Union

CE MDD

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/MDD NumberB-3233871XN Basic UDI-DI D-3233871XNUDI-DIDate29 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
RACCORDO ARMATO ALTA PRESSIONE RA/LLF cm 120(TUBO 1200 psi)
Model / Reference
DISPOSITIVI E ACCESSORI PER INFUSIONE E/O MONITORAGGIO, 3233871
Primary DI / UDI-DI
D-3233871XN
Basic UDI-DI
B-3233871XN
EMDN Code
A03010199 Infusion controllers - other
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000025272

Other devices from Med Italia Biomedica S.R.L

See all devices from Med Italia Biomedica 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