This oversight can be costly to the medical manufacturer in terms of product design expenses, compliance testing and certification turnaround time, and the device approval process. Medical products ...

UL evaluates more than 19,000 types of products, components, materials and systems annually with 20 billion UL Marks appearing on 72,000 manufacturers' products each year. UL's worldwide family of ...

The DPL series dc/dc converters offer 6-W of regulated output power with an industry standard DIP footprint and features UL 60601 medical approval. The series offers a 2:1 input range with nominal ...

Signal Transformer, a division of Bel Fuse Inc., recently announced that its high efficiency M4L Series of International Power Isolation Transformers has certified to numerous UL Safety Standards, ...

Given that the EU and FDA definitions of what constitutes a medical device encompass a large majority of medical products other than drugs, it is small wonder that the collective term ‘medical ...

Earlier this year the US followed the EU and Canada in moving to the3 rd edition of the IEC 60601-1 medical device standard. This change presents several challenges and adds layers of complexity for ...

IEC/EN 60950 is a set of guidelines for the electrical safety of equipment connected to the public power grid, or mains. Now in its 3rd edition, IEC/EN 60601-1 is a further series of technical ...