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Insufflatore Endotimpanico per Cateterismo Tubarico Vibrato (Ctv). Ctv/Af/230

by 4WELL Project S.R.L.

Ref PF1000101001Model INSUFFLATORE ENDOTIMPANICO PER CATETERISMO TUBARICO VIBRATO (CTV). CTV/AF/230

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08054754330083 Basic UDI-DI 08054754330083UDI-DIDate9 Oct 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  • Withdrawn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

Model / Reference
INSUFFLATORE ENDOTIMPANICO PER CATETERISMO TUBARICO VIBRATO (CTV). CTV/AF/230, PF1000101001
Primary DI / UDI-DI
08054754330083
Basic UDI-DI
B-08054754330083
EMDN Code
Z12159002 Aerosol equipment
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000038545

Other devices from 4WELL Project S.R.L.

See all devices from 4WELL Project S.R.L. →

Properties

  • Administering Medicine

Other properties (12)

  • Sterile: No
  • 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