The device master record contains current device specifications and. The document defines four types of records that are important for medical device development and manufacturing: 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,. Device master record index for amylase. The food and drug administration (fda) requires manufacturers of medical devices to create and maintain a device master record (dmr).
