As medical devices continue to get smaller in size, the assembly of the internal electronics becomes more critical. Like a puzzle, fitting all the necessary pieces together in a smaller space is no simple task. When outsourcing is involved, synergy between teams is critical. The earlier a medical device manufacturer’s design team and their contractor’s team begin working together, the better.
Selecting the best contract manufacturing partner can be a tricky process, especially for start-ups or companies new to the process. Since significant cost savings can be realized from working with a quality service provider, it is important for OEMs to identify key areas to make the process more efficient. This article outlines eight criteria to use during selection proceedings.
The Society of Women Engineers, along with the American Society of Mechanical Engineers recently honored Noha S. El-Ghobashy with the Kenneth Andrew Roe Award. El-Ghobashy is an inspiring humanitarian working tirelessly to bring opportunities and advancement to underdeveloped nations.
With the 3rd Edition of IEC 60601-1 impacting U.S. design engineers in June, it is critical they are aware of the implications to their medical device designs. For home healthcare devices, there is a collateral standard that will have a specific effect. This article focuses in on powering these products and the items in the standard of significance for that aspect.
As balloon catheters are used in critical therapeutic applications, they simply must work as they are intended. Therefore, testing these devices must ensure that failure will not occur. This article looks at the testing process for balloon catheters and what decisions manufacturers need to consider.
Medical electronic devices are no longer a trend; they are the reality of today’s healthcare environment. Seemingly, the number of powered medical devices far exceeds their non-powered counterparts. Even devices that had traditionally not been powered, such as the stethoscope, are now either being replaced by more effective electronic devices or being updated with electronics to function more efficiently and, more simply, better.
Design and development of a medical device is an exacting process, to say the least, and it assumes even more complexity because it almost always extends across years that encompass multiple iterations of the device. As a result, small things that were satisfactory in the prototype and first production run can grow to be problems that must be solved as production volume rises.
Given the number of device applications that involve the transfer of a gas or liquid, it is no wonder pump technology is such a significant part of many healthcare-related products. In addition, pumps are not exempt from the trends of miniaturization and cost reduction. As such, this article takes a look at how today’s medical device demands are being answered by advanced pump technology.
Much like other medical technology, implants are adapting to a post-depression economy brimming with new materials, new ideas, and ambitious plans for the future. The result is a focus on designing safer, more bio-compatible products for local markets.
To meet the needs of today’s healthcare professionals, medical instrumentation is getting smaller and made to be portable. That means the components in them need to be smaller, while still maintaining a high level of precision. This article will look at micro valve technology in portable medical devices.
Regardless of the indication, the technology, or the manufacturing process, all medical devices face thorough testing regimens to ensure they function as designed. There’s no room for error with any medical device, whether a low-tech orthopedic knee brace or a life saving pacemaker. The patient relying on the device they are using needs it to work perfectly.
A new formulation of synthetic, biochemically absorbable polymers is creating opportunities in the medical device and pharmaceutical fields. These “bioabsorbable polymers” are materials designed to dissolve into compounds that the body can safely absorb or eliminate.
New unique device identification labeling rules are on the way for medical devices, so it’s best for engineers to be aware of what impact they may have prior to them being mandatory. This article looks at the main points behind the coming rule and the considerations for ensuring proper symbol quality and label/mark verification.
Medical adhesives are often relied upon to provide the critical linkage between the body and a medical device. To effectively interface the two, adhesives are called upon to manage a host of factors at play at the skin/device interface, such as moisture and movement, and also control the environment with respect to things like microbial flora, odor, or skin hydration.
Diagnostic technology covers a broad range of equipment, tests, and medical fields, and recent advancements in technique and materials means that innovations are widespread and growing rapidly. Though economic conditions are preventing huge advancements in diagnostic imaging—if hospitals can’t afford the new technology, there is no point in designing it—the medical imaging community is focusing on refinement, rather than redesign.