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Category Archives: CE marking
Safety Fences and the Machinery Directive 2006/42/EC
While reading the new Guide to application of the Machinery Directive 2006/42/EC, Edition 2.1, I was interested to see that the last sentence in section 42, dealing with Safety Components and their status under the Machinery Directive, is this: Specific … Continue reading
Posted in CE marking, Machinery Directive 2006/42/EC
Tagged CE conformity, CE mark, CE marking, Machinery, Machinery Directive 2006/42/EC, Machinery Guide, Machinery Working Group, MD 2006/42/EC, Safety components, Safety Fences
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Guide to application of the Machinery Directive 2006/42/EC, Edition 2.1 – published in July 2017 and EN 61010-1 equipment
The Guide to application of the Machinery Directive 2006/42/EC, Edition 2.1, was published by the EC Commission in July. The link to the document is here. Be advised that is a direct download link. The “guideline” is extremely useful and … Continue reading
Posted in CE marking, Machinery Directive 2006/42/EC
Tagged CE marking, EN 60204-1, EN ISO 12100:2010, EN ISO 13849-1, Essential Health and Safety Requirements, Machinery Directive 2006/42/EC, MD 2006/42/EC
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ATEX Directive 2014/34/EU and the ATEX Directive 99/92/EC
The ATEX Directive 2014/34/EU applies to equipment used in mines and potentially explosive atmospheres. It is very common for the sales staff at F2 Labs to receive a request for technical assistance to comply with ATEX but it is not … Continue reading
Posted in CE marking
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The Exemption for Medical Devices Under the RoHS Directive Has Expired
The RoHS Directive 2011/65/EU, Article 4 (3) exclusion for industrial monitoring and control instruments expired on Saturday, July 22, 2017. That exclusion was used by quite a few manufacturers to delay RoHS compliance, but Article 4 (3) is now gone. … Continue reading
Posted in CE marking, EMC Directive 2014/30/EU, Low Voltage Directive 2014/35/EU, RoHS Directive 2011/65/EU
Tagged CE, CE consulting, CE marking, RoHS, RoHS 2011/65/EU
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Safety Components and the Machinery Directive 2006/42/EC
From time to time we are presented with a device that seemingly “fits” into the Low Voltage Directive 2014/35/EU because it only has electric function and no moving components. This would lead most to apply the Low Voltage Directive instead … Continue reading
Posted in CE marking, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC
Tagged CE mark, CE marking, EN 60204-1, EN 61010-1, EN ISO 12100:2010, Low Voltage Directive 2014/35/EU, LVD, LVD 2014/35/EU, Machinery Directive, Machinery Directive 2006/42/EC, MD 2006/42/EC, Safety components, Safety components for machinery
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CE marking and the ATEX Directive 2014/34/EU
Many times, we receive a request for assistance from a customer for a project that involves, “CE marking and ATEX.” While there is nothing wrong with calling ATEX out separately from other CE marking requirements, we note that the ATEX … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, Product Testing
Tagged ATEX, ATEX 2014/34/EU, ATEX Directive 2014/34/EU, ATEX Directive 94/9/EC, CE marking, CE product testing, Declaration of conformity, EC declaration of conformity, EMC 2014/30/EU, EMC Directive 2014/30/EU, EU declaration of conformity, Low Voltage Directive 2006/95/EC, Low Voltage Directive 2014/35/EU, LVD 2014/35/EU, Machinery Directive, Machinery Directive 2006/42/EC, MD 2006/42/EC
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The EU declaration of conformity
A frequent source of confusion for exporters of products to the EU is the EU declaration of conformity. Many customers that we assist are vaguely familiar with the concept and the role of the “DoC”. The EU declaration of conformity … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, EN 60601-1, General Product Safety Directive 2001/95/EC, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Regulation (EU)2017/745, 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
Tagged ATEX 2014/34/EU, ATEX 94/9/EC, CE marking, Declaration of conformity, EC declaration of conformity, EMC 2004/108/EC, EMC 2014/30/EU, EU declaration of conformity, EU-type Examination Certificate, Low Voltage Directive 2006/95/EC, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, New Legislative Framework, New Legislative Framework 2008, NLF 2008, Technical File
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CE marking and the Technical File
Manufacturers who send equipment into the EU are required to send a CE compliant product in most cases. This means that if you are making an electromechanical device, chances are that you will need to comply with at least one, … 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 Regulation (EU)2017/745, 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
Tagged ATEX 2014/34/EU, CE, CE marking, EMC 2014/30/EU, EMC Directive 2014/30/EU, EN 61326-1, Low Voltage Directive 2014/35/EU, RED 2014/53/EU, RoHS, RoHS 2011/65/EU, RoHS compliance, RoHS Directive 2011/65/EU, Technical File
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Repeal of the Affordable Care Act and the Medical Device Tax
Yesterday afternoon, March 6th, the House Republicans released the bill to repeal (most of) the Affordable Care Act, also known as Obamacare. Since F2 Labs is a safety compliance laboratory, helping many companies comply with regulatory issues when bringing their … Continue reading
Posted in EN 60601-1, Medical Devices Regulation (EU)2017/745, Product Testing
Tagged ACA, EN 60601-1, Medical Device, Medical device excise tax, Medical Device tax, Obamacare, Obamacare repeal bill
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Compliance Requirements for Lasers in the EU
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 CE, CE Certification, CE marking, CE marking lasers, EN 60825-1, F2 Labs, IEC 60825-1, Laser safety
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