Boston Scientific Corporation

2 dispositivos en la base de datos

  • Modelo / Serial
    Lot/Batch# EF0206 EF0300 EF5054 EF5062 EF5066 EF5113 EF5142 EF5187 5140F EF5188 EF5253 EFO017 EF0160 EF5069 EF5421 EF5547 EF5554
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide plus Argentina Austria Belgium Brunei Canada Chile China Colombia Czech Republic Denmark Finland France Germany Great Britain Hong Kong Hungary India Indonesia Ireland Israel Italy Latvia Lebanon Luxembourg Macau Malaysia Mexico Netherlands Norway Poland Portugal Puerto Rico Saudi Arabia. Singapore South Africa Spain Sweden Switzerland & Turkey
  • Descripción del producto
    The Peripheral Cutting Balloon Device small Monorail Delivery System features a balloon with 3 or 4 atherotomes (microsurgical blades) mounted longitudinally on its outer surface. When the Peripheral Cutting Balloon device is inflated, the atherotomes score the plaque, creating initiation sites for crack propagation. Percutaneous Transluminal Angioplasty (PTA) with the Peripheral Cutting Balloon Device allows dilatation of the target lesion with less pressure.
  • Modelo / Serial
    Lot/Batch# EF0341  EF0349  EF0350   EF0354 EF5047  EF5048  EF5093   EF5098  EF51 05  EF5168  EF5169  EF5170  EF5390  EF5396 EF5398  EF5404   EF5574  EE0914E  EF5046  EF5068  EF5198  EF5329 EF5562 EE0885E   EE0939E  EF0411  EF0429  EF5050  EF5051  EF5056  EF5095  EF5194  EF5273  EF5285  EF5341  EF5478  EF5566  EF5566''  EE0916E  EF5007  EF5086  EF5391  EE0937E  EF0351  EF5096  EF5235 EF5567 EE0915E   EF5067  EE0943E  EF5230  EF0213  EF5101  EF5172  EF5236  EF5573  EF0342  EF5217  EF5403  EE0924E  EF5102  EF5242  EF5296  EF5479  EE0932E  EF5286  EE0933E EF5209  EF5392  EFO028E  EF5004 EF5091  I   EF5229   EF5291   EF5564   EF0339   EF5222   EF5261   EF5397   EE0880E    EF0340   EF0343   EF0419   EF5092   EF5097   EF5100   EF51 04   EF5195 EF5243  EF5280  EF5287  EF5315    EF5331   EF5476   EF5485 EF5537  EF5563    EF0348   EF0353   EF5006   EF5171   EF5197    EF5314   EF5389   EF5497   EF5575   EF5368   EF5383   EF5363   EF5402   EF5379   EF5386   EF5387   EF5409   EF5401   EF5384   EF5571   EE0940E   EF5008 EF5282  EE0904E  EF0370  EF5049  EF5200   EF5272  EF5292  EF0345  EF5099  EF0204  EF5050  EF5267  EF5294  EE0917E  EF5293  EE0906E  EF5196  EF5388  EF5360  EF5385  EF5361  EF5588  EF5589  EFO057 EFO097  EF5109  EF5311  EF5481  EF5556  EFO033  EFO067  EF0150  EF0167  EF0407  EF5015  EF5020  EF5063  EF5110  EF5149  EF5249  EF5446  EF5461  EF5462  EF5551  EF5561  EF5615  EF0202  EF0315 EF0316    EF0317    EF0426      EF5073    EF5122    EF5441    EF5460    EF5501    EF5550    EF5586    EF5607      EFO041      EFO056    EFO078    EF0147    EF0163    EF0166    EF0193    EF0304    EF0319    EF0320    EF0409    EF5014    EF5016  EF5025  EF5114  EF5123  EF5139  EF5144  EF5145  EF5151  EF5183  EF5299  EF5300  EF5301  EF5302  EF5312  EF0208  EF5021  EF5023   EF5024  EF5027  EF5031  EF5037  EF5058  EF5065  EF5115  EF5132 EF5140  EF5585  EFO059  EFO068  EFOO77  EFO080  EFO095  EF0152  EF0162  EF0165  EF0201  EF0207  EF0305  EF0406   EF5022   EF5041   EF5060  EF5070  EF5085  EF5124   EF5125  EF5126  EF5127  EF5130 EF5147   EF5157   EF5158   EF5178   EF5185   EF5238   EF5248   EFO058   EFO069   EF0107   EF0158   EF0301   EF5083   EF5089   EF5116   EF5131   EF5146   EF5557   EE0881 E   EFO074   EF0127     EF0128     EF0129   EF0131 EF0132    EF0155    EF0168    EF5084    EF5090    EF5159    EF5179    EF5221    EF5241    EF5250    EF5558    EFOO08    EF0187    EF0323    EF5044    EF5045    EF5057    EF5121    EF5447    EF5500    EF5502    EF5606    EF01 06    EF0395  EF0424  EF5119  EF5150  EF5448  EF5498  EF5540  EF5580  EF0192  EF0199  EF0303  EF0396  EF0397  EF0398  EF5029  EF5035  EF5052  EF5088  EF5120  EF5141  EF5155  EF5156  EFO079  EF0157  EF0186 EF5079  EF5134  EF5451   EF5499  EF5541   EFOO09  RB43  EF0198   EF0302   EF5013  EF5017   EF5053    EF5059    EF5076    EF5148   EF5152    EF5310  EF5450   EF5503    EFOO07    EF0185    EF0292    EF5237    EF5452    EF5470 EF5548    EF0161    EF0322    EF5039   EF5080   EF5111   EF5440   EF5506   EF5549   EFO081   EF0299   EF5018   EF5465 EF5504    EF5555   EFO075   EFO093   EFO098   EF0115   EF0149   EF0151   EF0205     EF5087   EF5240 EF5251  EFO018  EFO094  EF5077  EF5420  EF5469  EF5519  EFO066  EF0105  EF0368  EF0379  EF5072  EF5078  EF5081  EF5112  EF5463  EF0428  EF5192  EF5262  EE0925E  EF5207  EF5263  EE0934E  EF0360 EF5094     EF5208   EF527 4   EF5279   EF5477   EF5565 EE0941 E    EF5005   EF5193   EF5265   EF5496   EF0352   EF0369   EF5103   EF5106   EF5216   EF5330   EF5486   EF5572   EFO017   EFO032   EF0114   EF0117   EF0321 EF5422  EF5521  EF5527  EFO016  EF0104 EF0116  EF0124  EF0148  EF0189  EF0365  EF0366  EF5107 EF5135  EF5532  EF5553  EFO052  EF0159  EF0296  CBM335015  EF0297  EF5074  EF5082  EF5464  EF5480  EF5505 EF5584  EF0408  EF0410  EF5061  EF5075  EF5475  EF5533 EF5587  EFO030   EF5033  EF5064  EF5108  EF5219  EF5220  EF5254  EF5449  EF5552  EF5599  EFO082  EF0421  EF5239  EF5252  EF5442  EF5518 EFO031  EF0156
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Nationwide plus Argentina Austria Belgium Brunei Canada Chile China Colombia Czech Republic Denmark Finland France Germany Great Britain Hong Kong Hungary India Indonesia Ireland Israel Italy Latvia Lebanon Luxembourg Macau Malaysia Mexico Netherlands Norway Poland Portugal Puerto Rico Saudi Arabia. Singapore South Africa Spain Sweden Switzerland & Turkey
  • Descripción del producto
    The Flextome Cutting Balloon Device consists of a balloon with 3 or 4 atherotomes (microsurgical blades) || mounted longitudinally on its outer surface. When the Flextome Cutting Balloon Device is inflated, the atherotomes score the plaque, creating initiation sites for crack propagation. This process, referred to as AtherotomyQ3J, allows dilatation of the target lesion with less pressure. The device is provided in 6 mm, 10 mm, and 15 mm lengths. The working length is the distance between the radiopaque marker bands. The proximal catheter shaft of the Flextome Cutting Balloon Device is a hypotube. This hypotube contains the inflation lumen for the balloon. The distal shaft is made of flexible material and contains two lumens. One lumen is for balloon inflation, and the second lumen is a guidewire lumen. The distal shaft is coated with a hydrophilic coating. The guidewire lumen is colored green for greater visibility. The guidewire exit port is 24 cm from the catheter tip. This port facilitates rapid exchanges. A needle with a luer port is included for flushing the wire lumen prior to the insertion of appropriate coronary guide wires. CLlPIT1M clips are provided to aid in handling of the catheter.

63 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    TDMDAT
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NIDFSINVIMA
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NIDFSINVIMA
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NIDFSINVIMA
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    AMPMDC
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