class III medical device Articles
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Keeping Your Business Compliant with FDA’s UDI Regulations
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 ...
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Why PTFE Tubing is the Tubing of Choice for Many Medical Device Manufacturers
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 ...
By Fluorostore
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