Device Recall Integris Allura

Fabricant

  • Adresse du fabricant
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA

4 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    All serial numbers
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution: US (Nationwide) including Puerto Rico and countries of: Albania, Algeria, US Virgin Islands, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Democratic Congo, Costa Rica, Croatia, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Germany, Greece, Guadeloupe, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of Kuwait, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Moldova, Morocco, Myanmar, Nepal, Netherlands, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Venezuela, and Vietnam.
  • Description du dispositif
    INTEGRIS Allura 9 (biplane); Model Number: 722021 || The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and interventional procedures. The Philips INTEGRIS Allura 12 & 15 system is intended for peripheral, abdominal, cerebral diagnostic and interventional angiography, neuro applications, cardiac applications and non-vascular interventions
  • Manufacturer
  • Modèle / numéro de série
    All serial numbers
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution: US (Nationwide) including Puerto Rico and countries of: Albania, Algeria, US Virgin Islands, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Democratic Congo, Costa Rica, Croatia, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Germany, Greece, Guadeloupe, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of Kuwait, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Moldova, Morocco, Myanmar, Nepal, Netherlands, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Venezuela, and Vietnam.
  • Description du dispositif
    INTEGRIS Allura 15-12 (mono); Model Number: 722043 || The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and interventional procedures. The Philips INTEGRIS Allura 12 & 15 system is intended for peripheral, abdominal, cerebral diagnostic and interventional angiography, neuro applications, cardiac applications and non-vascular interventions
  • Manufacturer
  • Modèle / numéro de série
    site numbers 534928, 545964, 532207, 545365, 538387, 543397, 543398, 543399, 546572, 544581, 544728, 548147, 547005, 539456, 543953, 547234, 547364, 545838, 545839, 545840, 544395, 547952, 530393, 545799, 540790, 547431, 544122, 541659, 546060, 543433, 545604, 543198, 545921, 545640, 545966, 541590, 540456, 546201, 541572, 544130, 544635, 534665, 542963, 535303, 541783, 544631, 540930, 544610, 544506, 546456, 544989, 544990, 544992, 543984, 543759, 546906, 543873, 543087, 543108, 547279, 546908, 544750, 545518, 545052, 545539, 543799, 543411, 547660, 543229, 544371, 548288, 546668, 545714, 537604, 541046, 544513, 545583, 540808, 545280, 548039, 544489, 544120, 540275, 540284, 540952, 544637, 547855, 545941, 545753, 541597, 545025, 536030, 544543, 546693, 548140, 546025, 545752, 547976, 543971, 543972, 539634, 545749, 546119, 545750, 547642, 544433, 545069, 545073, 547777, 547321, 547628, 545733, 547392, 545293, 545296, 547908, 541880, 543386, 546013, 548061, 545282, 533398, 541588, 541589, 540374, 545357, 542486, 545443, 546012, 545090, 545037, 538432, 532226, 540407, 103281, 104950, 531926, 104953, 530653, 520630
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Units were distributed to hospitals and medical centers nationwide.
  • Description du dispositif
    Philips Integris Allura x-ray systems angiographic - Allura 9 F/C (floor and ceiling models). A mono-plane analog Allura with a 9' Image Intensifier
  • Manufacturer
  • Modèle / numéro de série
    FCO 72200118 for 1st phase 72200132 for 2nd phase Equipment #'s 102560, 102948, 103128, 103265, 103331, 103561, 103562, 103564, 103780, 103781, 104075, 104149, 104464, 104501, 104514, 104515, 104642, 104670, 104890, 104925, 104952, 104954, 104955, 104956, 104957, 104958, 105081, 105082, 105136, 105140, 105157, 105186, 105191, 105390, 105402, 105598, 105615, 105655, 105656, 105674, 105779, 105784, 105912, 105940, 105946, 105947, 105960, 500028, 500029, 500038, 500042, 504493, 504659, 504665, 504666, 504730, 504750, 504770, 504789, 504792, 504797, 504798, 504806, 504807, 504872, 504913, 504915, 504916, 504940, 505106, 505107, 505281, 505486, 505538, 505572, 505587, 505651, 505668, 505679, 505707, 505719, 505759, 505805, 505809, 505861, 505925, 505989, 506047, 506049, 506148, 506169, 506170, 506178, 506230, 506232, 506322, 506370, 506397, 506403, 506408, 506476, 506538, 506564, 506616, 506621, 506637, 506654, 506657, 506658, 506785, 519115, 519198, 519211, 519213, 519214, 519533, 519534, 519535, 519537, 519541, 519548, 519576, 519594, 519677, 519680, 519733, 519738, 519771, 519812, 519899, 519901, 519989, 520004, 520236, 520251, 520309, 520430, 520431, 520481, 520523, 520524, 520525, 520680, 520681, 520761, 520809, 520882, 520956, 521131, 521223, 521318, 521320, 521463, 521537, 521545, 521650, 521661, 521711, 521763, 521769, 521770, 521802, 521853, 521854, 521892, 522038, 522065, 522118, 522119, 522135, 522162, 522177, 522191, 522243, 522245, 522247, 522250, 522293, 522418, 522440, 522446, 522458, 530361, 530370, 530390, 530421, 530459, 530460, 530463, 530662, 530669, 531651, 531753, 531805, 531806, 531813, 531837, 532074, 532080, 532178, 532215, 532246, 532292, 532445, 532534, 532535, 532612, 532613, 532615, 532616, 532617, 532652, 532986, 533085, 533236, 533286, 533343, 533401, 533418, 533619, 533796, 533861, 533922, 533967, 534160, 534218, 534221, 534233, 534237, 534251, 534268, 534427, 534440, 534476, 534477, 534478, 534479, 534630, 534681, 534717, 534743, 534758, 534813, 534874, 534876, 535224, 535250, 535342, 535614, 535728, 535979, 536090, 536425, 536639, 536777, 537020, 537065, 537644, 538269, 538763, 539099, 544478, 544479, 544502, 547870, and 553147   Addtional Equipment #s from phase 2 - 26161, 26166, 84444, 84489, 85013, 85041, 85093, 85094, 85126, 85128, 86061, 86065, 86144, 86272, 86319, 86320, 86322, 86332, 86360, 86435, 86456, 86494, 86501, 86572, 86575, 86583, 86933, 86971, 87013, 87318, 87339, 100316, 100328, 100434, 100470, 100475, 100521, 100585, 100587, 100613, 100643, 100645, 100658, 100701, 100704, 100714, 100783, 100788, 100810, 100811, 100866, 100913, 100945, 101036, 101073, 101309, 101433, 101434, 101485, 101566, 101589, 101609, 101610, 101619, 101620, 101864, 101965, 101973, 102000, 102001, 102009, 102037, 102083, 102094, 102103, 102160, 102161, 102179, 102493, 102502, 102629, 102632, 102675, 102676, 102710, 102715, 102746, 102791, 102842, 102863, 102870, 102874, 102944, 102953, 102983, 102995, 103002, 103004, 103021, 103022, 103026, 103029, 103034, 103070, 103148, 103170, 103182, 103183, 103193, 103201, 103211, 103214, 103238, 103246, 103248, 103255, 103257, 103335, 103355, 103356, 103379, 103382, 103494, 103518, 103709, 103712, 103714, 103743, 103823, 103828, 103906, 104057, 104107, 104111, 104145, 104148, 104194, 104198, 104337, 104382, 104403, 104411, 104412, 104415, 104424, 104426, 104427, 104463, 104511, 104516, 104529, 104630, 104631, 104797, 104909, 104933, 104941, 105243, 105254, 105305, 105489, 105511, 105731, 105733, 105736, 105737, 105773, 250005, 250071, 250084, 250300, 250333, 250581, 504530, 504536, 521359, 535601, 545636, 557810, 557839, 558192, 41726451, and 43234594.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution
  • Description du dispositif
    Integris Allura Flat Detector 9C
  • Manufacturer