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Cavi-T

by Dianosic - SAS France EUDAMED

Ref DBA02

EMDN Q030201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-03665870000047 Basic UDI-DIDate19 Feb 2024RegisteredStatusActive
European UnionCE/MDD NumberB-03665870000047 Basic UDI-DIDate19 Feb 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR, CE/MDD Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
DBA02
Primary DI / UDI-DI
03665870000047
Basic UDI-DI
B-03665870000047, 366587CAVITDX
EMDN Code
Q030201 Epistaxis catheters
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003648

Other devices from Dianosic - SAS

  • Cavi-T

    Class IIa

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (2)

  • EUDAMED eb068c8e-3e3a-4bb5-8a6d-7ea254dfcacd 61 fields · synced 22 Oct 2026
  • EUDAMED 03665870000047|366587CAVITDX 61 fields · synced 17 May 2026