Dublin, Nov. 21, 2024 (GLOBE NEWSWIRE) -- The "Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Training Course" conference has been added to ResearchAndMarkets.com's ...

Labeling Labeling techniques have undergone many changes since 1979. As a result, the industry has been required to develop new regulations and attitudes toward medical device labels. Dave Olson Dave ...

A number of healthcare groups are urging FDA to mandate the labeling of polyvinyl chloride (PVC) devices that contain di-2-ethylhexyl phthalate (DEHP). In a petition and letter sent to FDA in late ...

The medical device industry is evolving and expanding with every passing year, with new devices being developed to save lives and treat an array of ailments and health conditions. At the same time, ...

A medical device is an umbrella term for any instrument, software, or other article used alone or in combination for a medical purpose in humans. An estimated 2 million different kinds of medical ...

In furthering its efforts to modernize radio frequency (RF) equipment regulations, the Federal Communications Commission (FCC) recently codified rules that permit the electronic labeling (e-labeling) ...

The House on Thursday unanimously passed a bill to update federal device labeling rules, sending the legislation to the president’s desk. The E-Label Act would allow electronics manufacturers to meet ...

Singapore has widened a cybersecurity labelling initiative to include all consumer Internet of Things (IoT) devices such as smart lights, smart door locks, smart printers, and IP cameras. The scheme, ...