A device master record is a collection of every document needed to manufacture, package, and possibly service a medical device. The device master record is a regulatory requirement for all medical device companies. | medical device validation, regulation,. 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 food and drug administration (fda) requires manufacturers of medical devices to create and maintain a device master record (dmr).
