PIPELINE EMBOLIZATION DEVICE (25-35MM)

  • Model / Serial
    Model Catalog: FA-71500-30 (Lot serial: ALL LOT NUMBERS); Model Catalog: FA-77500-18 (Lot serial: ALL LOTS); Model Catalog: FA-77500-16 (Lot serial: ALL LOTS); Model Catalog: FA-77500-14 (Lot serial: ALL LOTS); Model Catalog: FA-77500-12 (Lot serial: ALL LOTS); Model Catalog: FA-77500-10 (Lot serial: ALL LOTS); Model Catalog: FA-77475-20 (Lot serial: ALL LOTS); Model Catalog: FA-77475-18 (Lot serial: ALL LOTS); Model Catalog: FA-77475-16 (Lot serial: ALL LOTS); Model Catalog: FA-77475-14 (Lot serial: ALL LOTS); Model Catalog: FA-77475-12 (Lot serial: ALL LOTS); Model Catalog: FA-77475-10 (Lot serial: ALL LOTS); Model Catalog: FA-77450-20 (Lot serial: ALL LOTS); Model Catalog: FA-77450-18 (Lot serial: ALL LOTS); Model Catalog: FA-77450-16 (Lot serial: ALL LOTS); Model Catalog: FA-77450-14 (Lot serial: ALL LOTS); Model Catalog: FA-77450-12 (Lot serial: ALL LOTS); Model Catalog: FA-77450-10 (Lot serial: ALL LOTS); Model Catalog: FA-77425-20 (Lot serial: ALL LOTS); Model Catalog: FA-77425-18 (Lot serial: ALL LOT
  • Product Description
    PIPELINE EMBOLIZATION DEVICE
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    SAINT-LAURENT
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    HC

One device with a similar name

Learn more about the data here

  • Model / Serial
    Model Catalog: FA-71500-25 (Lot serial: A090167); Model Catalog: FA-71400-25 (Lot serial: A090167); Model Catalog: FA-71450-25 (Lot serial: A090167); Model Catalog: FA-71475-25 (Lot serial: A090167); Model Catalog: FA-71425-25 (Lot serial: A090167); Model Catalog: FA-71375-25 (Lot serial: A090167); Model Catalog: 103-0602-300 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: 103-0601-300 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: 105-5055 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: FA-88810-40 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: FA-88810-50 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: FA-88810-30 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: FA-88810-20 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: FA-71500-25 (Lot serial: A090209); Model Catalog: FA-71400-25 (Lot serial: A090209); Model Catalog: FA-71450-25 (Lot serial: A090209); Model Catalog: FA-71475-25 (Lot serial: A090209); Model Catalog: FA-71425-25
  • Product Classification
  • Product Description
    PIPELINE EMBOLIZATION DEVICE (25-35MM);X-CELERATOR EXCHANGE HYDROPHILIC GUIDEWIRE - SS;MARATHON FLOW DIRECTED MICRO CATHETER;ALLIGATOR RETRIEVAL DEVICE;ULTRAFLOW HPC FLOW DIRECTED MICRO CATHETER
  • Manufacturer