Devices

Device Recall Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump

Fabricante

Stryker Instruments Div. of Stryker Corporation
  • Dirección del fabricante
    Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
  • Empresa matriz del fabricante (2017)
    Stryker
  • Source
    USFDA

Dispositivo con un nombre similar

Más información acerca de la data acá

Device Recall Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump
  • Modelo / Serial
    Lot Numbers: 8136753340 through 9131936639.
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- Including the United States, Argentina, Australia, Brazil, Canada, England, France, Germany, Hong Kong, Italy, Japan, Latin America, Malaysia, Mexico, Netherlands, New Zealand, Singapore, South Africa, Spain, Sweden, Switzerland and Taiwan.
  • Descripción del producto
    Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamazoo, MI; REF 0537-005-000.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation