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Duracuff® Pro ICFK Short, SIZE 7

by Andreas Fahl Medizintechnik-Vertrieb GmbH 2 variants

Ref 13096-07

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number405194811000DURAVEC++PP48 Basic UDI-DI 04051948167054UDI-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  • Withdrawn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
Duravec Pro PP
Model / Reference
13096-07
Primary DI / UDI-DI
04051948167054
Basic UDI-DI
405194811000DURAVEC++PP48
EMDN Code
R010503 Tracheostomy inner cannulas
Device Class
Class IIb
Medical Purpose
FAHL® tracheostomy tubes are intended to stabilise the tracheostomy following laryngectomy or tracheotomy. The tracheostomy tube is designed to keep the tracheostomy open. Tracheostomy tubes with cuff can be used for mechanical ventilation, including under anaesthesia. Percutan variants are designed for additional use in percutaneous dilatation tracheostomy.

Manufacturer details

EUDAMED SRN
DE-PR-000036717

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Properties

Other properties (1)

  • Sterile: No