Skip to content

DILATATORE VASCOLARE 16 F 20 cm(.038")

by Med Italia Biomedica S.R.L

Ref 803010Model DISPOSITIVI E ACCESSORI PER ACCESSO PERCUTANEO IN TECHNICHE DI CATETERIZZAZIONE

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-803010NP Basic UDI-DI D-803010NPUDI-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  • Withdrawn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
DILATATORE VASCOLARE 16 F 20 cm(.038")
Model / Reference
DISPOSITIVI E ACCESSORI PER ACCESSO PERCUTANEO IN TECHNICHE DI CATETERIZZAZIONE, 803010
Primary DI / UDI-DI
D-803010NP
Basic UDI-DI
B-803010NP
EMDN Code
C0504 Arterial introduction sets
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

Other properties (12)

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