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Medical Instruments and Devices

2018
Medical instruments and devices are all instruments, apparatus, devices, substances or other objects designed by the manufacturer for diagnostic or therapeutic use destined for the following purposes:1. Detection, prevention, monitoring, treatment or alleviation of diseases 2.
Elisabeth Presterl   +4 more
openaire   +2 more sources

Using Medical Device Logs for Improving Medical Device Design

2013 IEEE International Conference on Healthcare Informatics, 2013
User interfaces that employ the same display and buttons may look the same but can work very differently depending on exactly how they are implemented. In healthcare, it is critical that interfaces that look the same are the same. Hospitals typically have many types of visually similar infusion pumps, but with different software versions and variation ...
Abigail Cauchi   +3 more
openaire   +1 more source

The Medical Profession and the Medical Device Law

Archives of Surgery, 1978
The Medical Device Amendment of May 28, 1976, to the Food and Drug Act empowers the Food and Drug Administration to regulate and set standards for all medical devices from tongue blades to dialysis units. The FDA has set up "advisory panels" with consumer, industry, and professional representation to offer it advice as to whether particular devices ...
M S, Karlan, M B, Habal, D, Leake
openaire   +2 more sources

Medical device development

2009 Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2009
The development of a successful medical product requires not only engineering design efforts, but also clinical, regulatory, marketing and business expertise. This paper reviews items related to the process of designing medical devices. It discusses the steps required to take a medical product idea from concept, through development, verification and ...
openaire   +2 more sources

Medical device error

Critical Care Nursing Clinics of North America, 2002
This article discusses principal concepts for the analysis, classification, and reporting of problems involving medical device technology. We define a medical device in regulatory terminology and define and discuss concepts and terminology used to distinguish the causes and sources of medical device problems. Database classification systems for medical
openaire   +2 more sources

Medical devices.

Health Affairs, 2008
P. Bhatia
semanticscholar   +1 more source

Medical Device Security

The 26th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2005
Medical device security represents a growing problem within the healthcare industry. An increasing number of medical devices and systems contain critical health related information for which integrity, availability, and confidentiality must be maintained.
openaire   +2 more sources

The NCCLS and Medical Devices

JAMA: The Journal of the American Medical Association, 1980
Few practicing physicians are aware of the activities of the National Committee for Clinical Laboratory Standards (NCCLS), which was founded in 1968 when it grew out of a committee of the College of American Pathologists (CAP) as an interdisciplinary nonprofit organization. It provides a forum in the private sector that promotes the development and use
openaire   +2 more sources

A comprehensive review on additive manufacturing of medical devices

Progress in Additive Manufacturing, 2021
L. D. da Silva   +7 more
semanticscholar   +1 more source

Sales of Medical Devices – SAP Supply Chain

International Journal of Computer Trends and Technology, 2022
Pradeep Verma
semanticscholar   +1 more source

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