Device Recall Cardiovive 92531 automated external defibrillator

  • Modelo / Serial
    SERIAL NUMBERS: 331327, 331014, 331000, 331317, 330984, 341805, 341827, 341306, 341912, 338527, 341683, 335085, 338117, 341312, 340263, 341818, 341820, 341821, 341791, 341890, 338113, 338059, 341944, 338039, 338041, 335057, 341348, 338084, 338053, 341782, 338060, 341923, 338073, 338075, 341316, 340255, 338050, 340365, 341787, 341732, 341729, 341726, 340354, 338078, 341717, 338916, 341882, 341703, 341263, 341706, 335258, 338142, 341877, 340312, 341780, 341778, 338217, 341836, 338940, 340338, 335140, 341884, 341755, 334495, 341750, 341749, 341891, 338035, 334402, 335413, 341497, 338024, 335457, 341966, 341534, 338002, 341518, 341430, 338017, 341511, 338027, 341548, 341566, 341567, 341542, 341434, 335449, 341549, 381727, 381729, 381724, 341888, 341806, 341901, 338079 and 341790.
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- UNITED STATES, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHAMAS, BAHRAIN, BELARUS, BELGIUM, BERMUDA, BOLIVIA, BRAZIL, BULGARIA, CANADA, CAYMAN ISLANDS, CHILE, CHINA, COLOMBIA, COSTA RICA, CROATIA, CYPRUS, CZECH REPUBLIC, CZECHOSLOVAKIA, DENMARK, DOMINICAN REPUBLIC, ECUADOR, EGYPT, EL SALVADOR, FINLAND, FRANCE, GERMANY, GRECE, GUAM, GUATEMALA, HOLLAND, HONDURAS, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAQ, IRELAND, ISRAEL, ITALY, JAMAICA, JAPAN, JORDAN, KENYA, KOREA, KUWAIT, LEBANON, LIBYA, LITHUANIA, MALAYSIA, MALTA, MEXICO, MONACO, MORROCCO, NAMIBIA, NETHERLANDS, NEW CALEDONIA, NEW ZEALAND, NIGERIA, NORWAY, OMAN, PAKISTAN, PANAMA, PARAGUAY, PERU, PHILIPPINES, POLAND, PORTUGAL, PUERTO RICO, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SCOTLAND, SERBIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TRINIDAD & TOBAGO, TURKEY, UAE, UKRAINE, UNITED KINGDOM, URUGUAY, VENEZUELA, VIETNAM, VIRGIN ISLANDS AND YEMEN.
  • Descripción del producto
    Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). || Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Cardiac Science Corporation, 3303 Monte Villa Pkwy, Bothell WA 98021-8969
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA