Example – Post Market Surveillance Report

A Post Market Surveillance Report on a device manufacturer or device provides Product Liability Insurance Companies with the comprehensive adverse event metrics and trends they need to write better policies and reduce their risk.  Researching adverse events with FDA MAUDE is a nightmare, time consuming and you’re never sure you have all the information.  Device Events is superior to FDA MAUDE reporting allowing users to Search for adverse events by Device Manufacturer, Device Name, Brand, Model Number, Generic Name, etc. and have comprehensive metrics available in seconds.  Metrics include:

  • Adverse Event Reports; GUDID Records; Recalls
  • Report Type (Death, Injury, Malfunction, Other)
  • Report Source; Reporter Occupation
  • Company Name; Brand Name; Device Name; Generic Name
  • Product Code; Device Problem; Medical Specialty
  • Country Code; Time Period

VIEW EXAMPLE REPORT