Devices

Device Recall Digital Diagnost

  • Modèle / numéro de série
    Site numbers 103982, 104073, 105158, 105629, 504343, 505773.  Added sites: 104303, 38280, 44807, 59667, 76907, 76909, 76974, 82641, 82652, 82657, 82724, 83072, 83073, 84712, 84862, 84863, 86072, 86987, 86988, 102030, 102100, 102489, 102713, 102717, 102719, 102787, 102905, 102911, 103109, 103165, 103274, 103437, 103438, 103439, 103453, 103893, 103894, 103941, 104465, 104902, 104903, 104904, 104937, 104938, 105415, 105621, 105623, 105625, 105668, 250094, 250470, 250471, 250875, 500002, 504546, 504989, 505038, 505347, 505350, 505351, 505352, 505605, 505684, 505944, 506184, 506343, 506643, 506645, 506826, 506839, 506848, 519148, 519149, 519150, 519568, 519739, 519904, 520297, 520298, 520299, 520385, 520687, 520698, 520766, 520808, 520811, 520828, 520836, 520978, 520984, 520986, 521004, 521089, 521110, 521412, 521539, 521660, 521668, 521893, 521894, 521995, 521997, 522213, 522215, 522244, 522281, 522360, 522361, 522362, 522364, 522367, 522398, 522475, 530411, 530412, 530415, 530455, 530516, 530611, 530696, 530716, 530779, 530787, 530789, 530791, 530792, 530796, 530800, 530806, 531773, 531825, 531833, 531858, 531975, 531994, 531995, 532138, 532141, 532167, 532168, 532169, 532171, 532206, 532211, 532278, 532364, 532421, 532422, 532815, 532816, 532817, 532818, 533244, 533317, 533319, 533338, 533426, 533468, 533534, 533571, 533769, 533915, 533916, 533920, 533949, 533950, 534082, 534279, 534435, 534539, 534570, 534622, 534718, 534800, 534801, 534836, 534866, 535146, 535334, 535381, 535383, 535549, 535626, 535773, 535774, 535786, 535933, 536002, 536039, 536043, 536062, 536064, 536128, 536129, 536441, 536448, 536614, 536913, 536939, 537163, 537184, 537455, 537753, 537755, 537762, 537840, 537918, 537948, 537950, 537974, 538139, 538154, 538166, 538304, 538437, 538478, 539680, 540173, 540199, 540474, 540477, 542194, 543376, 545097, 549011, 549725, and 557777.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Units were distributed to 1543 hospitals and medical centers throughout the US. No international distribution from this firm.
  • Description du dispositif
    Philips Digital Diagnost X-Ray system
  • Manufacturer
    Philips Medical Systems North America Co. Phillips
  • 1 Event

Fabricant

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

3 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall Digital Diagnost 3.1.x. XRay system
  • Modèle / numéro de série
    DigitalDiagnost Upgrade Release 3.1.x to 3.1.3
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    USA(nationwide) Distribution to the states of : AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, NC, ND, NE, NH, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA and WI
  • Description du dispositif
    Philips DigitalDiagnost 3.1.x X-Ray System
  • Manufacturer
    Philips Electronics North America Corporation
Device Recall Digital Diagnost Rel 3
  • Modèle / numéro de série
    S/N:  SN11000009 SN11000012 SN11000014 SN11000015 SN11000016 SN11000017 SN11000025 SN11000029 SN11000013 SN11000020 SN11000022 SN11000005 SN11000008 SN11000010 SN11000003 SN11000019 SN11000034 SN11000004 SN11000018 SN11000023 SN11000024 SN11000006 SN11000007 SN11000011 SN11000026 SN11000027 SN11000028 SN11000002
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: USA (nationwide) including states of: NC, SC, TX, and WV; and countries of: Australia, Austria,Canada, Germany, Italy, Netherlands, Sweden, and Switzerland.
  • Description du dispositif
    Philips Digital Diagnost Rel 3, a radiographic system, digital || Intended use: Radiographic system, digital
  • Manufacturer
    Philips Healthcare Inc.
Device Recall Digital Diagnost, stationary radiographic system
  • Modèle / numéro de série
    Units distributed from November 2006 through March 2014.
  • Classification du dispositif
    Physical Medicine Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide: US: AL, AR, AZ, CA, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, WY / Worldwide including Canada & Mexico
  • Description du dispositif
    Digital Diagnost, stationary radiographic system; Models: 712020/22/25/26/50/52/54/55/57/60/62/80/81/82/85
  • Manufacturer
    Philips Medical Systems, Inc.