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Recent Posts
- Proposed Updates to MDR and IVDR for Europe
- NFPA 790 vs. NFPA 791: A Field Evaluator’s Guide to This Dynamic Duo
- Why Does EMC Testing of a Medical Device to IEC 60601-1-2, AIM 7351731, and/or Common EM Emitters Testing Have to be Conducted in Both Charging and Battery Modes? (Even When the Device Is Basically Just Napping on the Charger)
- Is My Specially Designed Equipment in the Scope of RoHS?
- Why ISO/IEC 17025 Accreditation Matters for Electrical Safety & EMC Testing | F2 Labs
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Author Archives: Peter Jolles
My product connects by USB, why do I need to comply with the Low Voltage Directive?
The question in the title of this blog article is frequently asked by our customers. Let’s break it down. See the LVD 2014/35/EU, Article 1, para 2: The Low Voltage Directive 2014/35/EU applies to products with a power input of … Continue reading
Posted in CE marking, EMC Directive 2014/30/EU, EU Battery Regulation (EU)2023/152, General Product Safety Regulation (EU) 2023/988, GPSR, GPSR (EU)2023/988, Low Voltage Directive 2014/35/EU, Product Testing, RoHS Directive 2011/65/EU
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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
Posted in CE marking, Product Testing, REACH, RoHS Directive 2011/65/EU
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Here is why it is important to select the right Power Supply
Most of our customers must comply with the EMC Directive 2014/30/EU prior to application of a CE marking to their products. This is because the EMC Directive is applicable to almost everything with active electronics. Unlike North American EMC compliance … Continue reading
Posted in CE marking, EMC Directive 2014/30/EU, General Product Safety Regulation (EU) 2023/988, GPSR, GPSR (EU)2023/988, Low Voltage Directive 2014/35/EU, Product Testing, Radio Equipment Directive 2014/53/EU, RoHS Directive 2011/65/EU, UL 94
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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
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Fender Guitars and EU compliance, interesting read
In the interest of full disclosure, I own a Fender American Professional Telecaster, in butterscotch blonde of course, and a Fender Custom ’57 Champ Amp. I love Fender products. If it says “Fender” on it… I am usually considering the … Continue reading
Posted in CE marking
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Machinery Directive 2006/42/EC – The text and the harmonized EN standards
Complying with any EU CE marking Directive will require a trip to one of many European Commission websites to assist with the process. They are great sources of information, I have them bookmarked, and one or more are open on … Continue reading
Posted in CE marking, Machinery Directive 2006/42/EC, Machinery Regulation (EU)2023/1230
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EN 60950-1 is still acceptable for EU compliance… for now.
We are starting to feel some effects of the upcoming replacement of EN 60950-1 by EN 62368-1. This is causing some confusion in the compliance world as well and we wanted to share a recent example that we were contacted … Continue reading
Posted in CE marking, General Product Safety Regulation (EU) 2023/988, GPSR, Low Voltage Directive 2014/35/EU, Radio Equipment Directive 2014/53/EU
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RoHS 3 and the new (EU)2015/863 Substances
Now that we have been under the ‘new’ EU RoHS for a few months I thought it would be a good time to write a brief article to cover some of the most commonly asked questions. What changed? RoHS 2011/65/EU … Continue reading
Posted in CE marking, RoHS Directive 2011/65/EU
Tagged (EU)2015/863, 2015/863, RoHS, RoHS3
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On The Need For Translations
This is an often-asked question, “Do I need to translate the manual for the EU and what do I need to translate?” The answer is everything that is needed top assemble, safely operate, maintain, and eventually dispose of the equipment … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, Consulting, EMC Directive 2014/30/EU, Low Voltage Directive 2014/35/EU, Pressure Equipment Directive 2014/68/EU, Radio Equipment Directive 2014/53/EU
Tagged CE marking, EU declaration of conformity
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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
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