Show results for
Refine by
Class Iii Ce Certified Medical Devices Articles & Analysis
2 articles found
The US Food and Drug Administration (FDA) requires that all medical devices are identified with a unique device identifier (UDI), in both human and machine-readable forms. These UDI regulations were put in place to enable healthcare providers and manufacturers to more quickly identify flawed devices, leading to faster recalls, and a reduction in medical errors. UDI regulations UDIs are unique ...
Medical device manufacturers are constantly looking to improve their device designs to increase their performance levels. There are a number of different trends in the medical device industry that manufacturers will have to consider when bringing a product to market. One of the most common trends in the medical device industry is to connect metals and plastic. Another is to enable “real ...