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ProLine XT PercuTrach® Cuff, Gr.10 mit atraumatischer Einführhilfe steril, nicht MRT geeignet

by Primed Halberstadt Medizintechnik GmbH

Ref 1022210Model ProLine und Optima PercuTrach Sets

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42502032PRI0804Y Basic UDI-DI 04250203265485UDI-DIDate10 Feb 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  • Withdrawn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

Model / Reference
ProLine und Optima PercuTrach Sets, 1022210
Primary DI / UDI-DI
04250203265485
Basic UDI-DI
42502032PRI0804Y
EMDN Code
R0105020101 Tracheostomic cannulas, cuffed, not reinforced, with fixed flange, and kits
Device Class
Class IIb
Medical Purpose
Perkutane Dilatationstracheotomie

Manufacturer details

EUDAMED SRN
DE-PR-000036373

From the manufacturer

Manufacturer's product page: PROLINE (XT) PercuTrach®

Related devices

Category: Tracheostomy tube, non-reinforced, non-customized, single-use

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Properties

  • Sterile