What does DHR stand for?

Device History 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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Double H Quarter Horses (Dover, OH) Division of Healthcare Quality Promotion (Centers for Disease Control and Prevention) Deficiency of Heart Qi Syndrome Danaher Motion Saro, AB De Heer (Dutch: Mister) Decay Heat Removal Department of Historic Resources (Virginia) Department of Human Resources Design History Record Développement des Hommes et de Leurs Ressources (French: Development of Women and Their Resources)		Digital Hardcore Records (record label) Digital Health Record Dihydrorhodamine Director of Human Resources Disaster Housing Resources Dong Hae Industrial Company (South Korea) Foreningen for Kortvuxna (Association for People of Short Stature in Sweden) Drosophila Hormone Receptor 3 de Havilland Residents Association (UK) Defense Human Resources Activity

Samples in periodicals archive:

The firm also failed to include the primary identification label and labeling for each device in the device history record.

PMA/IDE required for multiple IVD Research devices

The company also fell short in maintaining both device history records (DHRs) and device master records (DMRs.

FDA cites Healthline for issues with quality system, device records, ...

The firm had not maintained a complete device history record for the recent lot of the wound dressings received in September, including the dates of manufacturing, batch records of the anti-microbial drugs, records of inspection or testing of the wound dressings being produced and packaged by contractors, and records of the company's receiving inspection and labeling examination of the wound dressings.

Retro-Tech

The new company is expected to perform prototype building, pilot projects and device history records management.

Coghlin creates medical device Manufacturing Company

The firm did not retain identification labels for the MiniCAT CT System in the Device History Record (DHR) as required, nor did it maintain procedures to control document approval and distribution.

Xoran Technologies

Tmed, Columbia, TN, Nashville, TN, District Tmed, Columbia, TN, received a five-item 483 because its device history record (DHR) did not include complete acceptance records, and because of inadequate CAPA procedures.

Tmed nets 5-item 483 for inadequate device history record and CAPAs

Camstar, which first entered into the Medical Device market 18 months ago, provides quality and paperless device history record (DHR) systems to medical device manufacturers, such as drug eluting stents, defibrillators and optical equipment and lenses.

Camstar Hits $20 Million Milestone in Medical Device Market in the ...

Retro-Tech warned for QS, device design procedures