Results 5 found
September 25th, 2017
European Access for Industrial Control Panels

Manufacturers of Industrial Control Panels (ICP) who intend to sell their products into Europe must comply with applicable Directives and “Self-declare” by applying the CE Mark. Based on the ICP’s intended use, a manufacturer determines which of the following three directives is most appropriate: Low Voltage, Electromagnetic Compatibility (EMC), or Machinery. Engaging with a trusted… read more

March 3rd, 2017
Regulatory Changes to the EU Low Voltage Directive

To achieve regulatory compliance, it’s important for manufacturers to understand how various (and changing) standards apply to their products.  UL’s worldwide network of compliance experts helps manufacturers navigate national and regional standard requirements to quickly access more markets. Manufacturers and marketing teams experience first-hand the frustration associated with understanding the complexities of selling products worldwide…. read more

October 3rd, 2014
European Market Access

Certification Marks for European Market Access UL helps to provide access to multiple strategic markets around the world through the acceptance of the UL Mark. The CE Mark and UL-EU Mark For manufacturers focused on European markets, UL can provide all the testing and assessment services in one single evaluation, resulting in the UL-EU Mark… read more

April 25th, 2014
European Market Access

Certification Marks for European Market Access UL helps provide access to multiple strategic markets around the world through the acceptance of the UL Mark. The CE Mark and UL-EU Mark For manufacturers focused on European markets, UL can provide all the testing and assessment services in one single evaluation, resulting in the UL-EU Mark to… read more

January 29th, 2014
UL’s Notified Body Toolkit

The EU is one of the most attractive markets for medical device and IVD sales. UL’s Notified Body toolkit provides 34- pages of information on the EU regulatory system, including the classification rules, process for approvals and conformity assessment procedures. It also is a valuable reference document, with links to guidance documents, Interpretive documents and… read more