Medical Device Vigilance decision tree for Japan for class 2 devices.

Hi everyone...I am trying to put together Medical Device Vigilance decision tree for Japan for class 2 devices..i have couple of information on when to file a 15 day report and a 30 day report, but still struggling to get more information to put a flowchart....please share flowcharts/questionnaire/decision trees
 
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Also looking for what type of reports needs to be submitted to PMDA, like FSCA report? Electrical safety issue report something on those lines?
 
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