CATHETER, PERITONEAL

FDA product code GBW · Class 1 · 10 devices · 11 reports · 1 devices named in recalls

• ARROW IPN036986

  Teleflex Incorporated · CATHETER, PERITONEAL
  2 recalls0 reports
• ARROW IPN032635

  Teleflex Incorporated · CATHETER, PERITONEAL
  2 reports
• CARDINAL HEALTH 30414-025

  Cardinal Health 200, LLC · CATHETER, PERITONEAL
  2 reports
• Cook G05262

  Cook Incorporated · CATHETER, PERITONEAL
  1 report
• Cook G05267

  Cook Incorporated · CATHETER, PERITONEAL
  1 report
• Tenckhoff G09085

  Cook Incorporated · CATHETER, PERITONEAL
  1 report
• Cook G09269

  Cook Incorporated · CATHETER, PERITONEAL
  1 report
• Super Sheath CBDE (CBDE) CI12L25TP0038

  Togo Medikit CO.,Ltd. · CATHETER, PERITONEAL
  1 report
• CORE DYNAMICS CD8190

  Conmed Corporation · CATHETER, PERITONEAL
  1 report
• Medline DYND50428

  Medline Industries, Inc. · CATHETER, PERITONEAL
  1 report