Search F2 TechNotes
Categories
- ATEX Directive 2014/34/EU
- CE marking
- Consulting
- EMC Directive 2014/30/EU
- EN 60601-1
- FCC
- General Product Safety Directive 2001/95/EC
- IP Testing
- Lasers
- Listing
- 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
- Product Testing
- R&TTE Directive 1999/5/EC
- Radio Equipment Directive 2014/53/EU
- REACH
- RoHS Directive 2011/65/EU
- UL 60335-1
- UL 61010-1
- UL 62368-1
- UL 94
-
Recent Posts
- 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?
- My product recharges or powers from a USB cable, do I need to comply with the Low Voltage Directive 2014/35/EU?
Daily Archives: September 8, 2016
CE markings, Ex markings, and other EU markings claiming product compliance
Manufacturers who build equipment for sale to customers in the European Union may spend a lot of time learning about and understanding the process that is required in order to sell their products with a CE marking on it. Placing … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, 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, Product Testing, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU, RoHS Directive 2011/65/EU
Leave a comment