Device master record template $ 150.00 form/template used to organize and consolidate product information intended to provide the technical documentation details associated with a. The device master record contains current device specifications and. Going by the fda’s definition a dmr is: 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,. A device master record is a collection of every document needed to manufacture, package, and possibly service a medical device.
