What does DMR stand for?

Device Master Record

This definition appears very rarely and is found in the following Acronym Finder categories:

Information technology (IT) and computers

Other Resources:

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Department of Mental Retardation Depot Maintenance Review Derived Market Return Design Maturity Review Design Modification Request Designated Marksman Rifle Desktop Maintenance Required Detailed Mission Requirements Deuteron Magnetic Resonance Développement, Modernisation et Recherche (French: Development, Modernization and Research)		Dexy's Midnight Runners (band) Differential Microwave Radiometer Diffuse Microwave Radiation Diffuse Microwave Radiometer (Instrument aboard the Cosmic Microwave Background Explorer, COBE spacecraft) Digital Media Receiver Digital Media Remastering (IMAX Corp.) Digital Microwave Radio Digital Mobile Radio (open radio standard) Digital Modular Radio Dimensionally-Modeled Relational (data structure)

Samples in periodicals archive:

IVD did not establish and maintain procedures to ensure that device history records for each batch, lot or unit are maintained to demonstrate that the device is manufactured in accordance with the device master record and the Quality System regulations, the warning letter stated.

PMA/IDE required for multiple IVD Research devices

The inspection also revealed that the device master records "for all devices manufactured here do not identify the location (specific controlled document) where the specifications may be found.

Gebauer nets 7-item 483 for complaint handling and procedure failures

The firm did not have a Device Master Record that contained or referenced all of the drawing and production specifications, production procedures, quality assurance procedures, packaging and labeling specifications for each type of device manufactured.

Torbot Group/Jobskin Division

The company did not maintain a complete Device Master Record (DMR) that includes all the elements required.

Xoran Technologies

FDA also found there was a failure to include in the company's device history records complete acceptance records that demonstrated the device was manufactured in accordance with the device master records.

Validation failures trip up Troy Innovative Instruments

Specifically, the device master record for the ExamWorks D product has not been updated to reflect the correct version of the bill of materials and software version.

Merge Technologies hit with 7-item 483 and warning letter for not ...

QS/QC; Val; 14271W Troy Innovative Instruments: * Devices not in conformance with GMP/QS regulation * Failed to validate manufacturing processes * Did not include complete acceptance records to show the device was manufactured in accordance with device master records * Failure to ensure CAPA were effective

Troy Innovative Instruments Middlefield, OH, Nov. 1 (Cincinnati, OH)

For example, it did not have a Device Master Record for the Transilluminator that contained or identified the location of the device and component specifications, and other required information for the manufacturing processes.

Chiu Technical warned for CAPAs