Additional Feedback (The FDA requires all adverse events related to medical devices to be reported to http://www.fda.gov/Safety/MedWatch/default.htm. Per the required New Hire Training Course "WAO-MDR-Sales", all DePuy Sales Representatives are required to submit a Device Experience Report form to The Complaints Handling Unit within 48 hours of learning of an adverse event. The approved version of the DER form can be found on DePuy Edge. | 
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