Author Archives: Peter Jolles

Safety Fences and the Machinery Directive 2006/42/EC

Posted on October 10, 2017 by Peter Jolles

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 →

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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

Posted on September 19, 2017 by Peter Jolles

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 →

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ATEX Directive 2014/34/EU and the ATEX Directive 99/92/EC

Posted on September 5, 2017 by Peter Jolles

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 →

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Net Neutrality, what is it?

Posted on August 15, 2017 by Peter Jolles

I have been hearing a lot about “net neutrality” lately but I did not really know what it means, probably the same as most people, so I decided to find out. Read on. Basically, net neutrality means that no place … Continue reading →

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RoHS Directive 2011/65/EU – Article 4 (3) – expired

Posted on August 8, 2017 by Peter Jolles

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 , , , , | Leave a comment

Safety Components and the Machinery Directive 2006/42/EC

Posted on June 20, 2017 by Peter Jolles

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 →

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CE marking and the ATEX Directive 2014/34/EU

Posted on May 17, 2017 by Peter Jolles

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 →

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The EU declaration of conformity

Posted on May 10, 2017 by Peter Jolles

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 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 | Tagged , , , , , , , , , , , , , , , | Leave a comment

CE marking and the Technical File

Posted on April 7, 2017 by Peter Jolles

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 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 | Tagged , , , , , , , , , , , , | Leave a comment

Repeal of the Affordable Care Act and the Medical Device Tax

Posted on March 7, 2017 by Peter Jolles

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 →

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