MEDTRONIC CRYOCATH LP

7 devices in the database

  • Model / Serial
    Model Catalog: 3FC12 (Lot serial: 2399); Model Catalog: 3FC12 (Lot serial: 2308); Model Catalog: 3FC12 (Lot serial: 2442); Model Catalog: 3FC12 (Lot serial: 2443); Model Catalog: 3FC12 (Lot serial: 2444); Model Catalog: 3FC12 (Lot serial: 1919); Model Catalog: 3FC12 (Lot serial: 1920); Model Catalog: 3FC12 (Lot serial: 2288); Model Catalog: 3FC12 (Lot serial: 2309); Model Catalog: 3FC12 (Lot serial: 2391); Model Catalog: 3FC12 (Lot serial: 2390); Model Catalog: 3FC12 (Lot serial: 2389); Model Catalog: 3FC12 (Lot serial: 2364); Model Catalog: 3FC12 (Lot serial: 2363); Model Catalog: 3FC12 (Lot serial: 2348); Model Catalog: 3FC12 (Lot serial: 2340); Model Catalog: 3FC12 (Lot serial: 2400)
  • Product Description
    flexcath steerable sheath 3FC12
  • Model / Serial
    Model Catalog: FREEZOR 5 207F5 (Lot serial: ALL LOTS); Model Catalog: FREEZOR 3 207F3 (Lot serial: ALL LOTS); Model Catalog: FREEZOR 1 207F1 (Lot serial: ALL LOTS)
  • Product Description
    FREEZOR CARDIAC CRYOABLATION CATHETERS
  • Model / Serial
    Model Catalog: 3FC12 (Lot serial: >10 numbers contact mfg)
  • Product Description
    FLEXCATH STEERABLE SHEATH Model 3FC12
  • Model / Serial
    Model Catalog: 2FC12 (Lot serial: 01068); Model Catalog: 2FC12 (Lot serial: 00036); Model Catalog: 2FC12 (Lot serial: 00070); Model Catalog: 2FC12 (Lot serial: 00085); Model Catalog: 2FC12 (Lot serial: 00170); Model Catalog: 2FC12 (Lot serial: 00277); Model Catalog: 2FC12 (Lot serial: 00344); Model Catalog: 2FC12 (Lot serial: 00363); Model Catalog: 2FC12 (Lot serial: 00400); Model Catalog: 2FC12 (Lot serial: 00431); Model Catalog: 2FC12 (Lot serial: 50811); Model Catalog: 2FC12 (Lot serial: 50711); Model Catalog: 2FC12 (Lot serial: 50614); Model Catalog: 2FC12 (Lot serial: 50419); Model Catalog: 2FC12 (Lot serial: 50111); Model Catalog: 2FC12 (Lot serial: 01186); Model Catalog: 2FC12 (Lot serial: 01185); Model Catalog: 2FC12 (Lot serial: 01153); Model Catalog: 2FC12 (Lot serial: 01105); Model Catalog: 2FC12 (Lot serial: 01099); Model Catalog: 2FC12 (Lot serial: 00017); Model Catalog: 2FC12 (Lot serial: 01010); Model Catalog: 2FC12 (Lot serial: 01009); Model Catalog: 2FC12 (Lot serial: 00861); Model Catalog:
  • Product Description
    FLEXCATH STEERABLE SHEATH
  • Model / Serial
    Model Catalog: (Lot serial: 207FI 207F3 207F5); Model Catalog: (Lot serial: 21201)
  • Product Description
    F7 FREEZOR CARDIAC CRYOABLATION CATH
2 more

10 manufacturers with a similar name

Learn more about the data here

  • 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
    NZMMDSA
  • 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
    MSHM
  • 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
    AEMPSVFOI
  • 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
    BAM
  • 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
    MHSIDCCCDMIS
5 more