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PRIMEDISILK-VENT® Silikonkanüle, gesiebt, Gr.9 Länge 62 mm mit 22 mm Anschluss + 1 Beutel a 5 Stck Primediair-Phon UltraFlow

by Primed Halberstadt Medizintechnik GmbH

Ref 200625, 200629Model Trachealkanüle

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42502032PRI0685A Basic UDI-DI Date10 Apr 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  • Withdrawn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

Trade Name
PRIMEDISILK-VENT® Silikonkanüle, gesiebt, Gr.9 Länge 62 mm mit 22 mm Anschluss + 1 Beutel a 5 Stck Primediair-Phon UltraFlow
PRIMEDISILK-VENT® Silikonkanüle, Gr.9 Länge 62 mm mit 22 mm Anschluss + 1 Beutel a 5 Stck Primediair-Phon UltraFlow
Device Name
Primedisilk (Silikonkanülen)
Model / Reference
Trachealkanüle, 200625, 200629
Primary DI / UDI-DI
04250203217569, 04250203225014
Basic UDI-DI
42502032PRI0685A
EMDN Code
R0105010101 Tracheostomic cannulas, cuffless, not reinforced, with fixed flange, and kits
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004967

Other devices from Primed Halberstadt Medizintechnik GmbH

See all devices from Primed Halberstadt Medizintechnik GmbH →

Properties

Other properties (13)

  • Sterile: No
  • 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