Invacare Corporation

8 dispositivos en la base de datos

  • Modelo / Serial
    The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098, 10JF034099, 10JF034100, 10JF034101, 10JF034102, 10JF034103, 10JF034104, 10JF034105, 10JF034106, 10JF034107, 10JF034108, 10JF034109, 10JF034111, 10JF034112, 10JF034113, 10JF034114, 10JF034115, 10JF034116, 10JF034117, 10JF034119, 10JF034120, 10JF034121, 10JF034122, 10JF034123, 10JF034124, 10JF034125, 10JF034126, 10JF034127, 10JF034128, 10JF034129, 10JF034130, 10JF034131, 10JF034132, 10JF034133, 10JF034134, 10JF034135, 10JF034136, 10JF034177, 10JF034178, 10JF034179, 10JF034180, 10JF034181, 10JF034182, 10JF034183, & 10JF034184.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide distribution: USA including states of: FL, GA, KY, LA, MO, NC, NE, NJ and SC.
  • Descripción del producto
    HomeFill Oxygen Compressor IOH200 Homefill, The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098, 10JF034099, 10JF034100, 10JF034101, 10JF034102, 10JF034103, 10JF034104, 10JF034105, 10JF034106, 10JF034107, 10JF034108, 10JF034109, 10JF034111, 10JF034112, 10JF034113, 10JF034114, 10JF034115, 10JF034116, 10JF034117, 10JF034119, 10JF034120, 10JF034121, 10JF034122, 10JF034123, 10JF034124, 10JF034125, 10JF034126, 10JF034127, 10JF034128, 10JF034129, 10JF034130, 10JF034131, 10JF034132, 10JF034133, 10JF034134, 10JF034135, 10JF034136, 10JF034177, 10JF034178, 10JF034179, 10JF034180, 10JF034181, 10JF034182, 10JF034183, & 10JF034184. || The IOH 200 Homefill is an electromechanical, prescription device designed for use in the home. Its intended function and use is to provide supplemental oxygen to patients and to supply pressurized oxygen to fill cylinders for the patients personal ambulatory use.
  • Modelo / Serial
    Model Numbers: 0806281234, 0806893858, 0806135534, 0806161578, 0806237627, 0806268153, 0806268154, 0806309590, 0806315524, 0806351557, 0806568768, 0806591793. 0806670117, 0806724855, 0806731287, 0806773921, 0807007811, 0807019897, 0807062866, 0807110193
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Product was distributed to the following states: CA, CO, MN, NJ, OR, PA, TX & VA and one to Canada.
  • Descripción del producto
    Kuschall K Junior Manual wheelchair
  • Modelo / Serial
    06JE002273, 06JE002762, 06JE003580, 06JE003583, 06JE003584, 06JE003585, 06JE003597, 06JE003598, 06JE003880, 06JE003890, 06JE004170, 06JE004172, 06JE004178, 06JE004196, 06JE004632, 06JE004640, 06JE005420, 06JE005421, 06JE005864, 06JE005870, 06JE005871, 06JE005879, 06JE005885, 06JE006254, 06JE006277, 06JE006599, 06JE006603, 06JE006612, 06JE007087, 06JE007393, 06JE007396, 06JE007403, 06JE007408, 06JE007818, 06JE008028, 06JE008311, 06JE008322, 06JE008324, 06JE008329, 06JE008330, 06JE008332, 06JE008350, 06JE008670, 06JE008678, 06JE009028, 06JE009031, 06JE009039, 06JE009040, 06JE009042, 06JE009060, 06JE009062, 06JE009076,  06KE000147, 06KE000149, 06KE001924, 06KE001933, 06KE002243, 06KE002264, 06KE002265, 06KE002267, 06KE002270, 06KE002851, 06KE002853, 06KE002858, 06KE002862, 06KE003116, 06KE003379, 06KE003381, 06KE003386, 06KE003612, 06KE004451, 06KE004454, 06KE004455, 06KE004467, 06KE004854, 06KE005538, 06KE005826, 06KE006063, 06KE006065, 06KE006333, 06KE006613, 06KE006876, 06KE006877, 06KE006886, 06KE006894, 06KE007257, 06KE007282, 06KE007294, 06KE007450, 06KE007684, 06KE007686, 06KE007689, 06KE008610, 06KE008611, 06LE000170, 06LE000173 06LE001305, 06LE001313, 06LE001527, 06LE001694, 06LE001696, 06LE001697, 06LE001705, 06LE001998, 06LE002608, 06LE003258, 06LE003261, 06LE003267, 06LE003268, 06LE003462, 06LE003466, 06LE003987, 06LE004643, 06LE004650, 06LE004846, 06LE004857, 06LE005143, 06LE005144, 06LE005148, 06LE005152, 06LE005154, 06LE005732, 06LE005895, 06LE006012, 06LE006013, 06LE006024, 06LE006704, 06LE006707, 06LE006709, 06LE007018, 06LE007210, 06LE007358, 06LE007371, 06LE007379, 06LE007387, 06LE007393, 06LE007397, 06LE007403, 06LE007404, 07AE000983, 07AE001149, 07AE001180, 07AE001326, 07AE001327, 07AE001334, 07AE001594, 07AE001595, 07AE002009, 07AE002013, 07AE002223, 07AE002225, 07AE002229, 07AE002400, 07AE002404, 07AE002670, 07AE002683, 07AE002990, 07AE003522, 07AE003700, 07AE003712, 07AE003713, 07AE003716, 07AE004618, 07AE005103, 07AE005337, 07AE005339, 07AE005340, 07AE005341, 07AE005586, 07AE005593, 07AE005597, 07AE005886, 07AE005887, 07AE005895, 07AE006089, 07AE006303, 07AE006308, 07AE006314, 07AE006927, 07AE006930, 07AE007089, 07AE007090, 07AE007091, 07AE007092, 07AE007103, 07AE007105, 07AE007113, 07AE007114, 07AE007326, 07AE007327, 07AE007331, 07AE007334, 07AE007598, 07AE007606, 07AE007607, 07AE007611, 07AE007612, 07BE001073, 07BE001076, 07BE001077, 07BE001078, 07BE001082, 07BE001093, 07BE001303, 07BE001309, 07BE001310, 07BE001578, 07BE001585, 07BE001806, 07BE001810, 07BE002005, 07BE002014, 07BE002015, 07BE002253, 07BE002254, 07BE003336, 07BE003337, 07BE003569, 07BE003574, 07BE003582, 07BE003584, 7BE003585, 07BE004719, 07BE004907, 07BE004913, 07BE004916, 07BE006332.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide and Canada.
  • Descripción del producto
    Invacare Storm TDX Power Wheelchair, Models: #TDX3-PS, TDX3-SE-PS, TDX4-PS.
  • Modelo / Serial
    0805007204, 0805040231,0805087799, 0805191275, 0805238718, 0805528869, 0805590456, 0805007205, 0805040233, 0805094654, 0805202392, 0805260264, 0805528870, 0805590458, 0805007206, 0805046010, 0805112919, 0805202409, 0805260267, 0805528879, 0805598707, 0805007207, 0805052515, 0805112920, 0805202410, 0805265355, 0805538825, 0805606638, 0805031769, 0805052531, 0805112921, 0805208212, 0805265356, 0805547691, 0805606639, 0805032072, 0805052780, 0805142288, 0805214576, 0805488915, 0805556308, 0805606650, 0805032078, 0805059713, 0805148474, 0805220731, 0805528850, 0805556313, 0805626956, 0805032082, 0805059770, 0805171786, 0805220813, 0805528852, 0805573454, 0805636805 0805032091, 0805081690, 0805171787, 0805226782, 0805528854, 0805573455, 0805636810, 0805040230, 0805087792, 0805178698, 0805226965, 0805528856, 0805590391, 0805643631, 0805643632, 0805743810, 0805793490, 0805837237, 0805871475, 0805937131, 0806309254, 0805664651, 0805743813, 0805802652, 0805845927, 0805894716, 0805969761, 0806309260 0805671759, 0805771388, 0805802878, 0805845935, 0805894890, 0805977531, 0806309261, 0805685506, 0805776512, 0805807275, 0805850343, 0805894892, 0806273105, 0806309267, 0805702791, 0805776514, 0805807278, 0805855553, 0805900539, 0806281922, 0806315127, 0805710093, 0805780848, 0805807281, 0805860047, 0805900540, 0806281924, 0806315184 0805710275, 0805784712, 0805811158, 0805865040, 0805906053, 0806303957, 0806320300, 0805716215, 0805784713, 0805815571, 0805865041, 0805922688, 0806303963, 0806326394, 0805721816, 0805784714, 0805815575, 0805871470, 0805929066, 0806303965, 0806326395, 0805738220, 0805789076, 0805815809, 0805871471, 0805937122, 0806309167, 0806338838,  0806338840, 0806372582, 0806390080, 0806415186, 0806448589, 0805771388, 0806338842, 0806372583, 0806390081, 0806415385, 0806448735, 0806350846, 0806372585, 0806390082, 0806422077, 0806455546  0806350855, 0806372614, 0806390083, 0806428328, 0806463285, 0806355566, 0806372615, 0806396466, 0806428330, 0806463289, 0806366353, 0806372616, 0806408921, 0806428344, 0806463290, 0806366354, 0806372618, 0806408928, 0806428346, 0806480052,  0806366356, 0806372620, 0806408929, 0806428563, 0806480055, 0806366544, 0806390074, 0806408930, 0806435361, 0806480070, 0806372581, 0806390075, 0806408938, 0806441968, 0806488512.
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide and Canada.
  • Descripción del producto
    Kuschall''s K3/K4 Series of Manual Wheelchair, Model Airlite.
  • Modelo / Serial
    06FE009232
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide and Canada.
  • Descripción del producto
    Solara Spree XT (SPRXT) manual wheelchair.
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Más información acerca de la data acá

  • Dirección del fabricante
    Invacare Corporation, 1 Invacare Way, Elyria OH 44035-4190
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA
  • Dirección del fabricante
    Invacare Corporation, 1200 Taylor St, Elyria OH 44035-6248
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA
  • Dirección del fabricante
    Invacare Corporation, One Invacare Way, Elyria OH 44036
  • Source
    USFDA
  • Dirección del fabricante
    Invacare Corporation, 1 Invacare Way, Elyria OH 44035
  • Source
    USFDA
10 más