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PercuCurve(TM) Set, solo

by Teleflex Medical

Ref 121566-000000

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000304KF Basic UDI-DI 34026704933694UDI-DIDate5 Nov 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  • Withdrawn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
RÜSCH PercuCurve Percutaneous Tracheostomy Dilator Set
Model / Reference
121566-000000
Primary DI / UDI-DI
34026704933694
Basic UDI-DI
08019020000000000000304KF
EMDN Code
R010699 Percutaneous tracheostomy kits - other
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000015868

Other devices from Teleflex Medical

See all devices from Teleflex Medical →

Properties

  • Sterile
  • Reprocessed

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: 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