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LARYVOX® Puncture Set for primary tracheo-oesophageal puncture

by Andreas Fahl Medizintechnik-Vertrieb GmbH

Ref 25200

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number405194825200LRVXPNCTRPPK9 Basic UDI-DI 04051948100815UDI-DIDate6 Aug 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  • Withdrawn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
LARYVOX Puncture Set
Model / Reference
25200
Primary DI / UDI-DI
04051948100815
Basic UDI-DI
405194825200LRVXPNCTRPPK9
EMDN Code
R900399 Respiratory system surgery instruments, single-use - other
Device Class
Class IIa
Medical Purpose
The LARYVOX® Puncture Set is intended for making a primary or secondary tracheooesophageal puncture.

Manufacturer details

EUDAMED SRN
DE-PR-000036717

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Properties

  • Sterile