M.I.Tech Co., Ltd.

9 devices · 13 adverse event reports · 0 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-120-180

  Prosthesis, Esophageal
  3 reports
• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-150-230

  Prosthesis, Esophageal
  3 reports
• HANAROSTENT LowAxTM Duodenum/Pylorus(NNN) DNJF-22-120-230

  Stent, Metallic, Expandable, Duodenal
  1 report
• HANAROSTENT® LowAxTM Duodenum/Pylorus(NNN) DNJF-22-120-230

  Stent, Metallic, Expandable, Duodenal
  1 report
• HANAROSTENT® Esophagus TTS(CCC) ECBA-18-060-180

  Prosthesis, Esophageal
  1 report
• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-060-180

  Prosthesis, Esophageal
  1 report
• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-080-180

  Prosthesis, Esophageal
  1 report
• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-080-230

  Prosthesis, Esophageal
  1 report
• HANAROSTENT® Esophagus TTS(CCC) ECBA-20-100-180

  Prosthesis, Esophageal
  1 report