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Rota-Trach Inner Cannula Tracheostomy Tube

by Vitaltec Corporation EUDAMED

Active European Union

Ref 5510700, 5510800

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number471146749TT03ED Basic UDI-DIDate24 May 2024RegisteredStatusActive
European UnionCE/MDR Number471146749TT03ED Basic UDI-DIDate24 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD, CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Tracheostomy inner cannulas
Model / Reference
5510700, 5510800
Primary DI / UDI-DI
04711467491619, 04711467491626
Basic UDI-DI
471146749TT03ED, B-04711467491626
EMDN Code
R010503 Tracheostomy inner cannulas
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
TW-MF-000011422
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

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Properties

Show properties
  • Sterile
  • Endocrine Disruptor
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No