Tag Archives: EN 60825-1

F2 sorts out Compliance Requirements for you

Posted on July 30, 2019 by Peter Jolles

Manufacturers contact F2 Labs from around the world for assistance with EU regulations. While F2 Labs primarily focuses on electro-mechanical devices, including medical devices, we have also assisted many people with an understanding of what is legally required. An example … Continue reading →

Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EMC Directive 2014/30/EU, EU Battery Regulation (EU)2023/152, General Product Safety Regulation (EU) 2023/988, GPSR, Lasers, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Regulation (EU)2017/745, Pressure Equipment Directive 2014/68/EU, Radio Equipment Directive 2014/53/EU, REACH | Tagged , , , | Comments Off on F2 sorts out Compliance Requirements for you

Compliance Requirements for Lasers in the EU

Posted on February 24, 2017 by Peter Jolles

Laser devices sent to Europe are subject to specific safety requirements. Some of these requirements are applicable even if the rest of the device is seemingly innocuous. To start with, we will present a case where a device appears to … Continue reading →

Posted in CE marking, General Product Safety Directive 2001/95/EC, Lasers, Product Testing | Tagged , , , , , , , | Comments Off on Compliance Requirements for Lasers in the EU