A device master record is a collection of every document needed to manufacture, package, and possibly service a medical device. A lot of the documents are not in the device master record, but are referenced in the dmr as to where the document is located (document control office, engineering library,. Going by the fda’s definition a dmr is: Okay, here is a generic example of a dmr template for a medical device. The document defines four types of records that are important for medical device development and manufacturing: