Aortic stent

FDA product code PNF · Class 3 · 19 devices · 42 reports · 1 deaths reported · 0 devices named in recalls

• Minima Stent System - 6mm FG-0001

  Renata Medical, Inc. · Aortic Stent
  1 death10 reports
• CP Stent™ 614311

  B Braun Interventional Systems, Inc · Aortic stent
  6 reports
• CP Stent™ 614308

  B Braun Interventional Systems, Inc · Aortic stent
  3 reports
• CP Stent™ 614309

  B Braun Interventional Systems, Inc · Aortic stent
  3 reports
• CP Stent™ 614310

  B Braun Interventional Systems, Inc · Aortic stent
  3 reports
• Minima Stent System - 8mm FG-0002

  Renata Medical, Inc. · Aortic Stent
  2 reports
• CP Stent™ 614516

  B Braun Interventional Systems, Inc · Aortic stent
  2 reports
• CP Stent™ 614376

  B Braun Interventional Systems, Inc · Aortic stent
  2 reports
• CP Stent™ 614478

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614497

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614509

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• G-ARMOR STENT® 614761

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614307

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614363

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614367

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614368

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614371

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614375

  B Braun Interventional Systems, Inc · Aortic stent
  1 report
• CP Stent™ 614380

  B Braun Interventional Systems, Inc · Aortic stent
  1 report