Category Archives: REACH

The EU REACH Regulation and US manufacturers… here is what you need to know.

F2 Labs assists manufacturers around the world with compliance obligations. Historically we have been an accredited test laboratory for electrical, electro-mechanical, EMC, and radio testing. We expanded to offer services to our customers for the EU RoHS Directive 2011/65/EU in … Continue reading

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What Now?

A comprehensive guide into the listing standards that are required after testing to compliance marks. Continue reading

Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, FCC, FDA, Field Label, GPSR, GPSR (EU)2023/988, International Testing, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Machinery Regulation (EU)2023/1230, Medical Devices Regulation (EU)2017/745, PPE Regulation (EU) 2016/425, Pressure Equipment Directive 2014/68/EU, Prop 65, Radio Equipment Directive 2014/53/EU, REACH, RoHS Directive 2011/65/EU, SPE-1000, UKCA, US Field Label | Comments Off on What Now?

Great Britain Changed the UKCA Deadline for Implementation, Again

The COVID-19 pandemic has thrown us all for a loop. Effects of the pandemic have been seen across many industries, supply chains, and more, including the extension of deadlines for product compliance regulations. In a statement on August 24th, 2021, … Continue reading

Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, EN 60601-1, General Product Safety Regulation (EU) 2023/988, GPSR, GPSR (EU)2023/988, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Machinery Regulation (EU)2023/1230, Medical Devices Regulation (EU)2017/745, Pressure Equipment Directive 2014/68/EU, Product Testing, Radio Equipment Directive 2014/53/EU, REACH, RoHS Directive 2011/65/EU | Tagged | Comments Off on Great Britain Changed the UKCA Deadline for Implementation, Again

RoHS 2011/65/EU and (EU)2015/863 – What is the difference?

Understanding the requirements for compliance to RoHS 2011/65/EU is not difficult (and we can help you), but ignoring them can get your product stopped upon entry into the EU. RoHS stands for the “restriction of hazardous substances”. Initially, it restricted … Continue reading

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Rapid Alerts and RoHS in the European Union

I get an email from RAPEX every Friday morning that details products stopped in customs in the EU for various issues. These are not all of the of the products stopped, just the most dangerous ones. RAPEX is an acronym … Continue reading

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Is the CE marking still valid now that Brexit has happened?

Yes, for now. CE marking will be accepted until at least the end of 2020 and then the UKCA mark will be the replacement mark for products sent to the UK. The link to the official UK page regarding this … Continue reading

Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, EU Battery Regulation (EU)2023/152, General Product Safety Regulation (EU) 2023/988, GPSR, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Machinery Regulation (EU)2023/1230, Medical Devices Regulation (EU)2017/745, Pressure Equipment Directive 2014/68/EU, Radio Equipment Directive 2014/53/EU, REACH, RoHS Directive 2011/65/EU | Comments Off on Is the CE marking still valid now that Brexit has happened?

Important CE Marking Questions and Answers

Frequently at F2 Labs we get deep into various topics regarding CE marking and other compliance requirements. I can only imagine the sinking feeling that a manufacturer must feel when seeing this on a request for bid: CE marking required. … Continue reading

Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EMC Directive 2014/30/EU, EMC Testing, General Product Safety Directive 2001/95/EC, GPSR, 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, RoHS Directive 2011/65/EU | Comments Off on Important CE Marking Questions and Answers

F2 sorts out Compliance Requirements for you

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

RoHS 2011/65/EU – New Restrictions July 2019

RoHS 2011/65/EU presently requires compliance for electrical and electronic equipment to these six substances indicated in Annex II: We note that RoHS 2011/65/EU was amended by Commission Delegated Directive (EU) 2015/863 in March of 2015. The new restrictions are highlighted … Continue reading

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RoHS 2011/65/EU and a Tale of Three Guitars

The world has many good guitar manufacturers but it is commonly accepted that the very best guitars are made in the United States. Few guitar players will dispute that. In the world of acoustic guitars there are three ‘big’ manufacturers … Continue reading

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