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PAX-Extremitäten-Tourniquet

by X-CEN-TEK GmbH & Co.KG EUDAMED

Withdrawn No longer placed on the EU market

Ref 138103921

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42607454801625019A6 Basic UDI-DIDate1 Sep 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
PAX Behandlungssysteme (PBES)
Model / Reference
138103921
Primary DI / UDI-DI
04260745483032
Basic UDI-DI
42607454801625019A6
EMDN Code
V9003 Tourniquets
Device Class
Class I

Manufacturer details

EUDAMED SRN
DE-MF-000009521

Other devices from X-CEN-TEK GmbH & Co.KG

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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