Skip to content

Kaniula wewnętrzna

by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa 154 variants

Ref 45-1010

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59012921RTKAQT Basic UDI-DI 05901292110871UDI-DIDate26 May 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  • Withdrawn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
Tracheostomijna kaniula wewnętrzna
Model / Reference
45-1010
Primary DI / UDI-DI
05901292110871
Basic UDI-DI
59012921RTKAQT
EMDN Code
R010503 Tracheostomy inner cannulas
Device Class
Class IIb
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000010592

Other devices from SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

See all devices from SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa →

Properties

  • 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