Device Recall Guidant ASSURE ICD

  • Modelo / Serial
    Model B301: B301/100002, B301/100003, B301/100004, B301/100006, B301/100007, B301/100008, B301/100010, B301/100012, B301/100013, B301/100014, B301/100016, B301/100019, B301/100020, B301/100021, B301/100022, B301/100024, B301/100025, B301/100027, B301/100030, B301/100031, B301/100032, B301/100034, B301/100037, B301/100039, B301/100043, B301/100044, B301/100045, B301/100046, B301/100048, B301/100050, B301/100051, B301/100053, B301/100054, B301/100056, B301/100062, B301/100063, B301/100064, B301/100067, B301/100069, B301/100070, B301/100073, B301/100074, B301/100075, B301/100076, B301/100079, B301/100080, B301/100081, B301/100082, B301/100083, B301/100084, B301/100087, B301/100088, B301/100089, B301/100090, B301/100091, B301/100092, B301/100094, B301/100096, B301/100099, B301/100100, B301/100101, B301/100102, B301/100103, B301/100104, B301/100105, B301/100106, B301/100108, B301/100111, B301/100112, B301/100113, B301/100114, B301/100115, B301/100116, B301/100117, B301/100118, B301/100120, B301/100122, B301/100125, B301/100126, B301/100128, B301/100129, B301/100130, B301/100131, B301/100132, B301/100134, B301/100135, B301/100136, B301/100137, B301/100139, B301/100140, B301/100141, B301/100142, B301/100143, B301/100144, B301/100145, B301/100146, B301/100147, B301/100148, B301/100149, B301/100153, B301/100154, B301/100155, B301/100158, B301/100159, B301/100161, B301/100162, B301/100164, B301/100165, B301/100166, B301/100167, B301/100169, B301/100170, B301/100172, B301/100173, B301/100174, B301/100176, B301/100180, B301/100181, B301/100182, B301/100183, B301/100185, B301/100186, B301/100187, B301/100188, B301/100189, B301/100191, B301/100193, B301/100194, B301/100195, B301/100196, B301/100197, B301/100200, B301/100203, B301/100204, B301/100205, B301/100206, B301/100208, B301/100209, B301/100210, B301/100211, B301/100213, B301/100215, B301/100216, B301/100218, B301/100221, B301/100222, B301/100223, B301/100224, B301/100226, B301/100227, B301/100230, B301/100234, B301/100235, B301/100236, B301/100238, B301/100239, B301/100242, B301/100243, B301/100244, B301/100245, B301/100247, B301/100249, B301/100253, B301/100255, B301/100258, B301/100260, B301/100264, B301/100271, B301/100272, B301/100273, B301/100279, B301/100280, B301/100285, B301/100288, B301/100290, B301/100293, B301/100298, B301/100315, B301/100317, B301/100318
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    Worldwide
  • Descripción del producto
    Guidant ASSURE, Model B301, Implantable Cardioverter Defibrillator, ICD. (This model is not available in the USA) Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Boston Scientific CRM Corp, 4100 Hamline Ave N, Saint Paul MN 55112-5700
  • Source
    USFDA