Stylet, Ureteral

FDA product code EYA · Class 1 · 19 devices · 142 reports · 0 devices named in recalls

• ZIPwire™ M0066802220

  Lake Region Medical · Stylet, Ureteral
  46 reports
• ZIPwire™ M006630222B0

  Lake Region Medical · Stylet, Ureteral
  21 reports
• OLYMPUS GWH3505R

  Gyrus ACMI, LLC · STYLET, URETERAL
  16 reports
• ZIPwire™ M006630205B0

  Lake Region Medical · Stylet, Ureteral
  10 reports
• ZIPwire™ M0066802050

  Lake Region Medical · Stylet, Ureteral
  9 reports
• ZIPwire™ M0066802080

  Lake Region Medical · Stylet, Ureteral
  9 reports
• OLYMPUS GWH3505RA

  Gyrus ACMI, LLC · STYLET, URETERAL
  5 reports
• ZIPwire™ M006630209B0

  Lake Region Medical · Stylet, Ureteral
  5 reports
• OLYMPUS GWH3805R

  Gyrus ACMI, LLC · STYLET, URETERAL
  4 reports
• SureGlide 35BX

  Gyrus ACMI, LLC · STYLET, URETERAL
  3 reports
• ZIPwire™ M006630208B0

  Lake Region Medical · Stylet, Ureteral
  3 reports
• ZIPwire™ M0066802060

  Lake Region Medical · Stylet, Ureteral
  2 reports
• ZIPwire™ M0066802230

  Lake Region Medical · Stylet, Ureteral
  2 reports
• ZIPwire™ M0066802160

  Lake Region Medical · Stylet, Ureteral
  2 reports
• ZIPwire™ M0066802210

  Lake Region Medical · Stylet, Ureteral
  1 report
• SUREGLIDE 41BX

  Gyrus ACMI, LLC · STYLET, URETERAL
  1 report
• ZIPwire™ M006630206B0

  Lake Region Medical · Stylet, Ureteral
  1 report
• ZIPwire™ M006630200B0

  Lake Region Medical · Stylet, Ureteral
  1 report
• ZIPwire™ M006630216B0

  Lake Region Medical · Stylet, Ureteral
  1 report