Boston Scientific International S.A.

12 dispositifs dans la base de données

  • Modèle / numéro de série
    H74939277645110 H74939277690210 H74939277690220 H74939277845210 H74939277745210 H74939277645210 H74939277745110 H74939277665110 H74939277690110 H74939277765110 H74939277545110 H74939277690120 H74939277845110 H74939277790110 H74939277865110 H74939277545210 H74939277790220 H74939277665120 H74939277645220 H74939277645120
  • Classification du dispositif
  • Modèle / numéro de série
    WS5020 18225672, 18225673, 18225674, 18396812, 18401612, 18459184, 18581834, 18603231, 18682283, 18688431, 18688432, 18707084, 18736313, 18751534, 18751536, 18838165, 18845130, 18875658, 18900177, 18914801, 18914802, 18929298 WS5024 18396813, 18401613, 18408201, 18408202, 18435076, 18480472, 18492730, 18581835, 18591486, 18603232, 18682284, 18682288, 18688428, 18707085, 18736314, 18742868, 18751537, 18838166, 18866426, 18900176, 18914803, 18915361, 18934783, 18944586, 18972521, 18979870 WS5027 18396814, 18408203, 18409435, 18435077, 18459185, 18492731, 18581836, 18591490, 18682285, 18682289, 18707086, 18736315, 18751538, 18751539, 18838167, 18866427, 18876065, 18908883, 18914808, 18914809, 18914810, 18914811, 18914812, 18929299, 18934786, 18944584, 18944587, 18972522, 18979879, 18989184 WS5031 18396811, 18408205, 18435078, 18459186, 18534734, 18581837, 18591358, 18682286, 18707087, 18736316, 18752110, 18832856, 18845134, 18876063, 18893436, 18914813, 18934784, 18944588, 18980043, 18989186 WS5035 18182797, 18225668, 18225671, 18401059, 18435079, 18483583, 18581838, 18682287, 18707088, 18736317, 18751760, 18832857, 18845135, 18876066, 18900178, 18914814, 18934785
  • Modèle / numéro de série
7 en plus

7 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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.” Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
    BAM
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
    VNSAWH
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
    ORMPMDBP
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
    HPRA
2 en plus