UL announces the withdrawal of the First edition of the Standard for Electrical Equipment for Laboratory Use; Part 1: General Requirements, UL 61010A-1 and its' Part 2 standards; the First... read more →
On August 5, 2013, the U.S. FDA announced the extension of the transition date for IEC 60601-1 3rd edition from June 30, 2013 to December 31, 2013. This means FDA... read more →
Products today must meet a diverse spectrum of certification and compliance requirements, and there is a growing need to provide more transparency into products in the marketplace. In response to... read more →
European Union (EU) General Standard June 1, 2012 European Union (EU) Particular Standards Varies* Canada General Standard June 1, 2012 Canada Particular Standards Varies* United States of America (FDA) July... read more →
UL has recently been accredited by the Standards Council of Canada (SCC) as one of only two standards development organizations based outside of Canada. The accreditation enables UL to create... read more →
The IEC 60601-1 standard is a globally recognized standard for electro-medical equipment safety, and a parent standard over 60 particular device standards. The third edition (3rd), issued in 2005, has... read more →