Human Factors and Ergonomics

Unique device identifier

Stories

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Briefs: IoMT
September 2023 marked the 10-year anniversary of the day the FDA’s Unique Device Identification (UDI) requirement first took effect. In that time, UDI went from an idea to a framework to a law; its GUDID database now uniquely identifies and holds data on more than 4 million medical devices and is the foundation for thousands of daily lookups and transactions.
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Briefs: Connectivity
As the industry continues to implement new supply-chain solutions like RFID for improved visibility, patients can look forward to a future where timely access to critical drugs and medical devices is assured, and the quality of care is greatly enhanced.
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Ask the Expert

Ralph Bright on the Power of Power Cords
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Understanding power system components and how to connect them correctly is critical to meeting regulatory requirements and designing successful electrical products for worldwide markets. Interpower’s Ralph Bright defines these requirements and explains how to know which cord to select for your application.

Inside Story

Inside Story: Trends in Packaging and Sterilization
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Eurofins Medical Device Testing (MDT) provides a full scope of testing services. In this interview, Eurofins’ experts, Sunny Modi, PhD, Director of Package Testing; and Elizabeth Sydnor, Director of Microbiology; answer common questions on medical device packaging and sterilization.

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