Fortify

  • Modelo / Serial
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    U.S. Nationwide distribution
  • Descripción del producto
    Fortify, Sterile EO, Model #/ Part #: || CD1231-40/100029238,100030095, 100041981; || CD1231-40Q/100029229, 100030087, 100041982; || CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; || CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; || CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; || CD1235-40Q/100029273, 100029295, 100029312, 100030840; || CD1241-40/100046351; || CD1241-40Q/100046167; || CD2231-40/100029274, 100030110, 100041922; || CD2231-40Q/100029275, 100030089, 100041923; || CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; || CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; || CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; || CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; || CD2241-40/100046148; || CD2241-40Q/100046149; || CD2299-40/100056952
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    St Jude Medical Inc., 15900 Valley View Ct, Sylmar CA 91342-3577
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    USFDA

50 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
  • Descripción del producto
    (1) - (12) Automatic implantable defibrillator, implantable biventricular pacing pulse generator with defibrillation function
  • Manufacturer
  • Modelo / Serial
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q; Fortify ST VR, Model Numbers: CD1241-40 and CD1241-40Q; Fortify Assura VR, Model Numbers: CD1257-40, CD1257-40Q, CD1357-40C, CD1357-40Q; Fortify Assura ST VR, Model Numbers: CD1263-40, CD1263-40Q, CD1363-40C, CD1363-40Q; Fortify DR, Model Numbers: CD2231-40 and CD2231-40Q; Fortify ST DR, Model Numbers: CD2241-40 and CD2241-40Q; Fortify Assura DR, Model Numbers: CD2257-40, CD2257-40Q, CD2357-40C, CD2357-40Q; Fortify Assura ST DR, Model Numbers: CD2263-40, CD2263-40Q, CD2363-40C, CD2363-40Q || Product Usage Fortify and Fortify Assura implantable cardioverter defibrillators (ICDS) are intended to provided ventricular anti-tachycardia pacing and ventricular defibrillation for automated treatment of life threatening ventricular arrhythmias. The devices may also be programmed to provide single or dual chamber bradycardia pacing
  • Manufacturer
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