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Preguntas frecuentes
Créditos
Devices
Device Recall Philips Digital Diagnost VE
Modelo / Serial
Site numbers: 82652, 82681, 82723, 82730, 83073, 85495, 85696, 85697, 85698, 86222, 86382, 86383, 86987, 86988, 100572, 100806, 101933, 102030, 102100, 102115, 102116, 102117, 102489, 102539, 102596, 102713, 102717, 102719, 102787, 102905, 103109, 103165, 103262, 103271, 103272, 103436, 103437, 103438, 103439, 103453, 103511, 103778, 103893, 103894, 103953, 103971, 103976, 104014, 104338, 104465, 104578, 104673, 104676, 104864, 104902, 104903, 104904, 104937, 104938, 105158, 105198, 105199, 105322, 105367, 105415, X1641, X1642, X1650, X1767, X1768. The firm uses site numbers instead of serial numbers.
Clasificación del producto
Radiology Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
The firm distributed to medical facilities nationwide.
Descripción del producto
Digital Diagnost VE
Manufacturer
Philips Medical Systems Sales & Service Region No. America
1 Event
Retiro De Equipo (Recall) de Device Recall Philips Digital Diagnost VE
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Fabricante
Philips Medical Systems Sales & Service Region No. America
Dirección del fabricante
Philips Medical Systems Sales & Service Region No. America, 22100 Bothell Everett Highway, Bothell WA 98041
Source
USFDA
Language
English
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한국어