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Drentech Surgical Drenaggio Redon Con Trocar Ch 18

by Redax S.p.A 2 variants

Ref 14323Model Drentech Emotrans Dune completo c/autotrasfusione

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803413929DRENTECH2a6L Basic UDI-DI 08034139291963UDI-DIDate21 Sep 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Drentech Emotrans Dune completo c/autotrasfusione
Model / Reference
Drentech Emotrans Dune completo c/autotrasfusione, 14323
Primary DI / UDI-DI
08034139291963
Basic UDI-DI
803413929DRENTECH2a6L
EMDN Code
B0499 Autotransfusion devices - other
Device Class
Class IIa
Medical Purpose
The Emotrans Dune system is intended for thoracic and mediastinal drainage and for the postoperative recovery and autotransfusion of autologous blood, with optional connection to a cell salvage system.

Manufacturer details

EUDAMED SRN
IT-PR-000041363

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Properties

  • Sterile