Publication year: 2012
Source:Nurse Education Today
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Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.733056?ai=1lgu&mi=3s94u5&af=R
Source: http://www.tandfonline.com/doi/abs/10.1080/10401334.2012.715254?ai=16j&mi=3deric&af=R
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Source: http://www.tandfonline.com/doi/abs/10.1080/10401334.2012.715255?ai=16j&mi=3deric&af=R
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Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.733058?ai=1lgu&mi=3s94u5&af=R
Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.728672?ai=1lgu&mi=3s94u5&af=R
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Source: http://www.tandfonline.com/doi/abs/10.1080/10401334.2012.715264?ai=16j&mi=3deric&af=R
The medical industry’s continued technological progress with electronics integration requires consideration of a broad range of new connector parameters. Between smaller, more portable diagnostic equipment with advanced functionality, and ever-evolving complex machines like MRI, CAT, and other diagnostic and monitoring applications, choosing an effective connector solution takes time and careful selection of new parameters. Moving beyond contact resistance, current rating, and working voltage, following are several new ones to add to the old list.
Source: http://www.mdtmag.com/articles/2012/12/interconnect-considerations-demanding-medical-equipment
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Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.728673?ai=1lgu&mi=3s94u5&af=R
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Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.745908?ai=1lgu&mi=3s94u5&af=R
Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.744169?ai=1lgu&mi=3s94u5&af=R
MEDICAL TECHNOLOGY AT HOME: SAFETY-RELATED ITEMS IN TECHNICAL DOCUMENTATION.
Int J Technol Assess Health Care. 2013 Jan 7;:1-7
Authors: Hilbers ES, de Vries CG, Geertsma RE
Abstract
Objectives: This study aimed to investigate the technical documentation of manufacturers on issues of safe use of their device in a home setting. Methods: Three categories of equipment were selected: infusion pumps, ventilators, and dialysis systems. Risk analyses, instructions for use, labels, and post market surveillance procedures were requested from manufacturers. Additionally, they were asked to fill out a questionnaire on collection of field experience, on incidents, and training activities. Results: Specific risks of device operation by lay users in a home setting were incompletely addressed in the risk analyses. A substantial number of user manuals were designed for professionals, rather than for patients or lay carers. Risk analyses and user information often showed incomplete coherence. Post market surveillance was mainly based on passive collection of field experiences. Conclusions: Manufacturers of infusion pumps, ventilators, and dialysis systems pay insufficient attention to the specific risks of use by lay persons in home settings. It is expected that this conclusion is also applicable for other medical equipment for treatment at home. Manufacturers of medical equipment for home use should pay more attention to use errors, lay use and home-specific risks in design, risk analysis, and user information. Field experiences should be collected more actively. Coherence between risk analysis and user information should be improved. Notified bodies should address these aspects in their assessment. User manuals issued by institutions supervising a specific home therapy should be drawn up in consultation with the manufacturer.
PMID: 23290519 [PubMed - as supplied by publisher]
Source: http://www.ncbi.nlm.nih.gov/PubMed/23290519?dopt=Abstract
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Dip molding may not be a term that readily comes to mind when surgeons begin complicated procedures. Yet, without this sophisticated, highly controllable process, many medical devices used daily in hospitals could not meet stringent certification requirements.
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Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.733057?ai=1lgu&mi=3s94u5&af=R
Source: http://informahealthcare.com/doi/abs/10.3109/03091902.2012.728676?ai=1lgu&mi=3s94u5&af=R