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Preguntas frecuentes
Créditos
Devices
Device Recall CARESCAPE Monitor B850, B650 or B450
Modelo / Serial
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide Distribution: US nationwide, UNITED KINGDOM, UNITED ARAB EMIRATES, TURKEY, TAIWAN, SWITZERLAND, SWEDEN, SPAIN, SOUTH AFRICA, SLOVENIA, SLOVAKIA, SINGAPORE, SERBIA, SAUDI ARABIA, RUSSIAN FEDERATION, ROMANIA, REUNION, QATAR, PORTUGAL, POLAND, PHILIPPINEs, PARAGUAY, PANAMA, NORWAY, NEW ZEALAND, NETHERLANDS, MYANMAR, MOROCCO, MEXICO, MALAYSIA, LITHUANIA, LEBANON, LATVIA, JORDAN, JAPAN, JAMAICA, ITALY, ISRAEL, IRELAND, IRAQ, INDONESIA, INDIA, ICELAND, HUNGARY, GREECE, GIBRALTAR, GERMANY, FRANCE, FINLAND, ESTONIA, EGYPT, ECUADOR, DENMARK, CZECH REPUBLIC, CYPRUS, CROATIA, CHILE, BRUNEI, BERMUDA, BELGIUM, BANGLADESH, AUSTRIA, AUSTRALIA.
Descripción del producto
GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.
Manufacturer
GE Healthcare, LLC
1 Event
Retiro De Equipo (Recall) de Device Recall CARESCAPE Monitor B850, B650 or B450
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Fabricante
GE Healthcare, LLC
Dirección del fabricante
GE Healthcare, LLC, 3000 N Grandview Blvd, Waukesha WI 53188-1615
Empresa matriz del fabricante (2017)
General Electric Company
Source
USFDA
Language
English
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