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TuBo-Guard Set weiß

by Novo Klinik-Service GmbH

Ref 20-50-7Model Mehrteilige Fixierung für Endotrachealtuben

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, self-declared

Class I: no certifier involved

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/MDR Number426040264V180YZ Basic UDI-DI 04260402641560UDI-DIDate8 May 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Mehrteilige Fixierung für Endotrachealtuben, 20-50-7
Primary DI / UDI-DI
04260402641560
Basic UDI-DI
426040264V180YZ
EMDN Code
R01038099 Endotracheal tubes - accessories not included in other classes
Device Class
Class I
Medical Purpose
Fixierung für orale Endotrachealtuben, Doppellumentuben, Larynxtuben und Larynxmasken. Zur Anwendung bei Jugendlichen und Erwachsenen geeignet.

Manufacturer details

EUDAMED SRN
DE-PR-000019606

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Properties

Other properties (1)

  • Sterile: No