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Preguntas frecuentes
Créditos
Devices
Device Recall StayFix
Modelo / Serial
Lot numbers: 551268, 551537, 551615, 551616, 551702, 551703, 551704, 553104, 553360, 553361, 553362, 553363, 554362, 554367, 554368, 554483, 554497, 554504, 554505, 554506, 554723, 554764, 554765, 554766, 555638, 555639, 555655, 555656, 555657, 555658, 556406, 556407, 556408, 556409, 556410, 556411, 556842, 556843, 556844, 556845, 556846, 556847, 556871, 556872, 556873, 556874, 556875, 562518, 562748, 562874, 563254, 563255, 563388, 563389, 566538, 566899, 566900, 566901, 566902, 566903, 566904, 567248, 567515, 567596, 567599, 567600, 567601, 567767, 567835.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Worldwide, including USA, France, Germany, and United Kingdom.
Descripción del producto
StayFix Fixation Device for Percutaneous catheters, REF 680ME, (small) 5F - 14F, Merit Medical, Unomedical, Ltd., Great Britain.
Manufacturer
Merit Medical Systems, Inc
1 Event
Retiro De Equipo (Recall) de Device Recall StayFix
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Fabricante
Merit Medical Systems, Inc
Dirección del fabricante
Merit Medical Systems, Inc, 1600 West Merit Pkwy, South Jordan UT 84095-2416
Source
USFDA
Dispositivo con un nombre similar
Más información acerca de la data
acá
Device Recall StayFix
Modelo / Serial
Lot Numbers: 547745, 551172, 554699, 555705, 555706, 556394, 556395, 556396, 556876, 556877, 558988, 560767, 560768, 560781, 561127, 561144, 562749, 562750, 563256, 563257, 563387, 564684, 564685, 565284, 565285, 565353, 565955, 566684, 566905, 566906, 566907, 567383, 567513, 567728, 569474.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Worldwide, including USA, France, Germany, and United Kingdom.
Descripción del producto
StayFix Fixation Device for Percutaneous catheters, REF 685ME, (large) 12F - 22F, Merit Medical, Unomedical, Ltd., Great Britain.
Manufacturer
Merit Medical Systems, Inc
Language
English
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