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Recent Posts
- Authorized EU Representative Requirement for EU Shipments
- UKCA mark and CE marking – September 2020 update from F2 Labs
- F2 Labs customer receives US FDA approval for a device used in the battle against COVID-19
- RoHS 2011/65/EU and (EU)2015/863 – What is the difference?
- NOTICE: We are offering PRO-BONO services – Can we help you?
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Tag Archives: EU
CE marking Onsite Consulting and Training
F2 Labs is able to send a CE marking expert to your facility to provide overview training to your business – sales and engineering. We can quickly dig into the Directives that apply to your specific products and show your … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EN 60601-1, General Product Safety Directive 2001/95/EC, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Directive 93/42/EEC, PPE Regulation (EU) 2016/425, Pressure Equipment Directive 2014/68/EU, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU, REACH, RoHS Directive 2011/65/EU
Tagged CE, CE mark, CE marking, EU, European Commission, European Union
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