A voluntary agreement (link in Dutch) was consummated by the Dutch Ministry of Health, industry, and hospitals. According to an Emergo blog post, under the terms of the agreement, the Netherlands will ...
Device-specific information must be included on Medicare claims forms or patient safety will not improve, says Cybele Bjorklund, a Distinguished Visitor at the O'Neill Institute for National and ...
Global data centre operator DayOne, affiliated with China's GDS Holdings , is planning to list simultaneously in Singapore and the U.S. in a move that is set to raise $5 billion, the Financial ...
The FDA’s device center has posted a draft guidance that addresses unique device identifier (UDI) code requirements applied to low-risk products. The select update offers enforcement discretion in ...
Every medical device has its own unique code, allowing manufacturers to keep track of their products once they enter the market. But while these codes are critical for recalling faulty devices or ...
(Reuters) - The U.S. Food and Drug Administration issued a long-awaited rule on Friday requiring companies to include codes on medical devices that will allow regulators to track the products, monitor ...
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