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Tag Archives: CE marking
The Machinery Directive 2006/42/EC and lifting accessories
The Machinery Directive 2006/42/EC, broadly, is applicable to machinery, defined in Article 2 (a) as an assembly fitted or intended to be fitted with a drive assembly to perform a function. The power, unless used for lifting purposes, must come … Continue reading
New RoHS restrictions, substances added to Annex II
There is a change on the horizon for manufacturers used to complying with RoHS based on the restriction of the six substances indicated in RoHS 2011/65/EU (Annex II): Lead (0.1%) Mercury (0.1%) Cadmium (0.01%) Hexavalent chromium (0.1%) Polybrominated biphenyls (PBB) … Continue reading
Compliance with the Low Voltage Directive 2014/35/EU, Annex I
F2 Labs is constantly working to help customers better understand their responsibilities in complying with CE marking Directives that may or may not apply to their equipment. Previously we published an article about the relationship between the Low Voltage Directive 2014/35/EU … Continue reading
Posted in CE marking, Low Voltage Directive 2014/35/EU, Product Testing, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU
Tagged CE, CE mark, CE marking, EN 60950-1, EN 61010-1, EN 62368-1, Low Voltage Directive 2006/95/EC, Low Voltage Directive 2014/35/EU, LVD, LVD 2014/35/EU, R&TTE, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU, RED 2015/53/EU
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CE marking Directives and the Authorized European Representative
The CE marking is placed on products after compliance with all applicable EU CE marking Directives. Some typical examples of CE marking Directives that F2 Labs provides technical support for are indicated below: Machinery Directive 2006/42/EC Low Voltage Directive 2014/35/EU … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Directive 93/42/EEC, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU
Tagged ATEX Directive 2014/34/EU, Authorized EU Representative, Authorized European Representative, Authorized Representative, CE, CE marking, Declaration of conformity, EC declaration of conformity, Electromagnetic Compatibility Directive 2014/30/EU, EMC Directive 2014/30/EU, EU declaration of conformity, EU Rep, EU Representative, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Radio Equipment Directive 2014/53/EU, RED 2014/53/EU
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EN standards and the Radio Equipment (RED) Directive 2014/53/EU and the Radio and Telecommunication Terminal (R&TTE) Directive 1999/5/EC
The Radio Equipment Directive 2014/53/EU, or RED, came into force in June of this year. This new Directive replaced the Radio and Telecommunications Terminal Equipment Directive 1999/5/EC for wireless equipment, also called the R&TTE Directive. There is a one-year transition … Continue reading
Posted in CE marking, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU
Tagged 2014/53/EU, CE, CE mark, CE marking, EC declaration of conformity, EN 300 328, EN 301 489-1, EN 301 489-17, EN standards, EU declaration of conformity, EU-type examination, Harmonized EN standards, R&TTE, R&TTE 1999/5/EC, R&TTE Directive 1999/5/EC, Radio and Telecommunications Terminal Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU, RED 2014/53/EU, RTTE Directive, SAR testing
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Harmonized EN standards, CE marking Directives and your European projects
Silently and slowly – but inexorably… the Directives and standards we use for CE marking are updated, revised, and replaced – and we must account for them. They must be correct when referenced on your declarations of conformity and that … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, Low Voltage Directive 2014/35/EU, Machinery Directive 2006/42/EC, Medical Devices Directive 93/42/EEC, PPE Regulation (EU) 2016/425, Product Testing, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU, RoHS Directive 2011/65/EU
Tagged CE, CE consultation, CE marking, CE product testing, CEN, CENELEC, EN ISO 12100:2010, EN ISO 13849-1, EN ISO 13849-1:2008, EN ISO 13849-1:2015, EN standards, Harmonized EN standards, IEC, ISO, Machinery Directive, Machinery Directive 2006/42/EC, MD 2006/42/EC
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The Radio Equipment Directive and the Simplified EU Declaration of Conformity
I first read the new Radio Equipment Directive 2014/53/EU (aka the “RED”) in 2014 when it was published and noted its similarity to the other NLF Framework Directives as it pertains to the documentation compliance process and the conformity modules. … Continue reading
Posted in ATEX Directive 2014/34/EU, CE marking, EMC Directive 2014/30/EU, 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 CE, CE Certification, CE consulting, CE marking, CE marking certification, CE product testing, Declaration of conformity, EC declaration of conformity, EU certification, EU compliance, EU declaration of conformity, European compliance, Radio Equipment Directive 2014/3/EU, RED 2014/53/EU, RED CE marking
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CE marking and the China Export mark
There are two commonly used markings on equipment that are very similar in appearance but mean different things. The CE marking is a European compliance marking and indicates compliance to all applicable European CE marking Directives (like the Machinery Directive … Continue reading
The EMC Directive and “Fixed Installations”
A common discussion point with manufacturers is the notion of the “fixed installation”. Probably mostly due to recital (36) in the beginning of the EMC Directive 2014/30/EU: Fixed installations are clearly defined in Article 3 (1.) (3.) of the EMC … Continue reading
RoHS Directive 2011/65/EU – Equipment for Research and Development
The understanding of many CE marking Directives is enhanced oftentimes by comparing a specific product to the recitals, articles, and annexes of the Directive and a detailed reading of the accompanying guidance document that is usually available to read alongside … Continue reading