Devices

Device Recall Single shot needle

  • Modèle / numéro de série
    0712528672, 20130203, 20140416, 20140608, 20140715, 5024221299, 5045228649, 5053234209, 5088247906, 5122261789, 5132266598,  5146272239, 5167280675, 5187287781, 5192290486, 5206296116,  5217302034, 5220302789, 5223304300, 5241310864, 5269320113,  5283325627, 5306337319, 5332345740, 5342350289, 5353356034,  6004360561, 6030372974, 6054381259, 6069391284, 6090400764,  6116413482, 6129418991, 6135420666, 6152427566, 6163432689,  6173438178, 6181441544, 6205450444, 6229462810, 6250470745,  6268479131, 6314501888, 6355519500, 7037541404, 7061552958,  7074559123, 7109575212, 7143589689, 7214621894, 7239632668,  8023698983, 8039708241, 8066720745, 8105737999, 8148758187,  8177772498, 8231796752, 8261810747, 8277818564, 8302830742 and  9029881729.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    22G x 70mm/20 bevel Single Shot Needle, REF 552-022-70, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
  • 1 Event

Fabricant

Stryker Instruments Div. of Stryker Corporation
  • Adresse du fabricant
    Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
  • Société-mère du fabricant (2017)
    Stryker
  • Source
    USFDA

7 dispositifs médicaux avec un nom similaire

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Device Recall Single shot needle
  • Modèle / numéro de série
    20130202, 20130415, 20140421, 20140609, 5046231227, 5076244238, 5122261790, 5143269915, 5167280677, 5187287779, 5206296117, 5223302038, 5269320118, 5283325629, 5306337317, 5332345739, 5339349276, 6025365183, 6041378163, 6074391286, 6088396277, 6124416923, 6135420668, 6150423728, 6172437516, 6187443411,  6201449651, 6226460917, 6250470746, 6269479417, 6286486660,  6321504502, 6335510754, 7010527909, 7033539866, 7068555924, 7085564091, 7106573430, 7134586527, 7180607419, 7192611056, 7240632667, 7333675532, 7355686304, 8039708245, 8052714217, 8070721005, 8105738000, 8148758189, 8150759733, 8172770405, 8191778149, 8225794524, 8231796797, 8276817903, 8289824215,  8301830046, 8330847601, 8357862273 and 9009870299.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    21G x 90mm/20 Bevel Single Shot Needle, REF 55-021-090, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
Device Recall Single shot needle
  • Modèle / numéro de série
    20130217, 20140414, 20140507, 20140527, 20140528, 20140610, 20140716, 5046231300, 5101251562, 5122261791, 5133266600,  5153274678, 5157276042, 5187287783, 5200294494, 5208298022,  5241310863, 5269320112, 5283325624, 5291331195, 5306337318, 5319341187, 5332345743, 5342350291, 6004356829, 6004360560, 6037374453, 6054381257, 6061387795, 6073391292, 6088396287, 6090400765, 6107408674, 6121415236, 6135420667, 6150423848, 6158429977, 6163432688, 6172437498, 6174438863, 6186443028, 6221458770, 6255473157, 6283486655, 6313500842, 6321504503, 6342514077, 6353518040, 7005525171, 7026536490, 7037541403, 7054549741, 7068555927, 7074559182, 7107573680, 7142589688,  7176604912, 7184608177, 7192611054, 7263643184, 7290656233,  7330674022, 7330674024, 7355686009, 8022698982, 8039708180 8045710627, 8052714216, 8070721966, 8105737996, 8148758188, 8150759732, 8176772079, 8191778150, 8226795127, 8277818561, 8302830726, 9009870015 and 9029881744.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    22G x 50m/20 bevel Single Shot Needle, REF 552-022-050, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
Device Recall Single shot needle
  • Modèle / numéro de série
    5070237478, 5101251566, 5126264328, 5167280678, 5187287785, 5259317857, 5283325626, 5342350292, 6054381263, 6088396285, 6160431974, 6172437501, 6264477580, 6335510755, 7005525170, 7012528659, 7026536489, 7033539877, 7059551767, 7061552956 7074559142, 7099569799, 7107574179, 7165600823, 7214621893, 7234630667, 7262643183, 7333675530, 7333675534, 8002688356, 8105738001, 8225794525, 8231797179, 8232797381 and  9009870341.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    21G x 150m/20 bevel Single Shot Needle, REF 552-021-150, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
Device Recall Single shot needle
  • Modèle / numéro de série
    5024221300, 5066234842, 5098251564, 5108256483, 5122261793, 5241310866, 5332345742, 6025365198, 6054381265, 6124416924,  6135420665, 6179440931, 6198447630, 6263476609, 6353518297,  7037541401, 7061552957, 7109575215, 7263643185, 7333675531, 8002688741, 8070721007, 8203783830 and 8277818567.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    24G x 25mm/20 bevel Single Shot Needle, REF 552-024-025, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
Device Recall Single Shot Needle
  • Modèle / numéro de série
    20130402, 20130417, 5157276046, 5241310865, 5322341821, 6025365199, 6054381261, 6088396279, 6103407344, 6140423727, 6160431976, 6173438180, 6192445451, 6236465683, 6261475102, 6289489211 7054549736, 7066554360, 7081561706, 7113575378, 7143590434, 7176604919, 7192611077, 7240632671, 7263643188, 8002688742, 8056715166, 8105738336, 8177772499, 8204783981, 8231797107, 8277818566 and 8302830744.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    22G x 50mm/45 Bevel Single Shot Needle, REF 554-022-050, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
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