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 from other than human power (electrical, hydraulic, pneumatic, etc.).

‘Lifting accessories’ which, among some other products (which will be the subject of later articles), are not ‘machinery’ as defined in Article 2 (a) and can be as simple as a C-hook or a purpose-built piece of metal used to prop open and hold a cowling on an aircraft during maintenance. Lifting accessories that are permanently attached to lifting machinery are not considered as lifting accessories, the definition is meant to encompass the device between the lifting machinery and the load itself.

Lifting accessories are defined in Article 2 (d):

Another example is an engineered hook used to attach to something to lift it up: such as an engine or an engine part. An engineered piece of metal used in this way, though with no moving parts or electrical components, would require a full evaluation against the requirements of the Machinery Directive 2006/42/EC, Annex I, plus a CE marking, declaration of conformity, and a Technical File.

This means that in order to claim compliance and put a CE marking on your lifting accessory you will need to contact a laboratory experienced with EN ISO 12100:2010 and probably at least one other standard, possibly falling on the C-type standards list as published by the European Commission. For the example immediately above, this is likely the harmonized C-type Machinery Directive EN standard:

EN 13155:2003+A2:2009 Cranes – Safety – Non-fixed load lifting attachments

The EU Commission has published some information for your review if you are unsure regarding where your equipment fits, as pertains to Article 2 (d). See some helpful links below.

F2 Labs is here to help. Have a question or a comment? We can be contacted via this link. We can be reached by phone at 877-405-1580 and are here to help you.

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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) (0.1%)
  • Polybrominated diphenyl ethers (PBDE) (0.1%)

The change is Commission Delegated Directive (EU) 2015/863 published in the Official Journal of the European Union on March 31, 2015.

This new Directive makes the following change to the above list of restricted substances by adding four new substances:

  • Bis(2-ethylhexyl) phthalate (DEHP) (0.1%)
  • Butyl benzyl phthalate (BBP) (0.1%)
  • Dibutyl Phthalate (DBP) (0.1%)
  • Diisobutyl phthalate (DIBP) (0.1%)

The Directive is very short, only three pages, and below are three notable sections.

  • Article 2 – 2015/863 is applicable to all RoHS products effective July 22, 2019
  • Annex II – medical devices, including in vitro medical devices, and monitoring and control instruments, including industrial monitoring and control instruments are exempted from these new restrictions until July 22, 20121
  • Annex II – some of the substance restrictions indicated in 2015/863 are current substance restrictions applicable to toys per the REACH Regulation 1907/2006.

Finally, note that Article 2 of the new Directive requires that all EU Member States adopt this Directive and publish “…laws, regulations and administrative provisions necessary to comply with this Directive.”

F2 Labs is here to help. Have a question or a comment? We can be contacted via this link. We can be reached by phone at 877-405-1580 and are here to help you.

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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 and the Machinery Directive 2006/42/EC. Besides the LVD’s relationship with the MD, a question that comes up over and over is the need to comply with the Low Voltage Directive 2014/35/EU for some products that are seemingly not in the scope of this law at all.

The Low Voltage Directive 2014/35/EU scope of applicability is indicated in Annex I, paragraph 2, and is:

This Directive shall apply to electrical equipment designed for use with a voltage rating of between 50 and 1 000 V for alternating current and between 75 and 1 500 V for direct current, other than the equipment and phenomena listed in Annex II.

This means that electrical equipment with an input power of from 50 to 1,000 volts AC and from 75 to 1,500 volts DC are within the scope of the law. Battery powered devices that operate with an input power of 12 volts DC are therefore excluded from the law.

Unfortunately, it is not that simple. For example, if you have a product that operates on 12 volts DC power but you supply an AC/DC adapter with your product when you ship to the EU then your product is operating with an input power of 230 volts AC and it is within the scope of the Low Voltage Directive. Similarly, if you do not supply the power supply with the product but you specify that an AC/DC power supply must be used with your product then it is considered an AC powered product and therefore will operate at 230 volts AC power and is within the scope of the LVD.

Also note that both the Radio and Telecommunications Terminal Equipment Directive 1999/5/EC and the Radio Equipment Directive 2014/53/EU require compliance with Annex I of the LVD no matter the voltage.

See below Article 3 (1.) (a) from the R&TTE Directive 1999/5/EC:

  1. The following essential requirements are applicable to all apparatus: (a) the protection of the health and the safety of the user and any other person, including the objectives with respect to safety requirements contained in Directive 73/23/EEC, but with no voltage limit applying;

 Note that Directive 73/23/EEC was the Low Voltage Directive in effect when 1999/5/EC was written. By law that refers to, now, the Low Voltage Directive 2014/35/EU.

See below Article 3 (1.) (a) from the Radio Equipment Directive 2014/53/EU (also called the “RED”):

  1. Radio equipment shall be constructed so as to ensure: (a) the protection of health and safety of persons and of domestic animals and the protection of property, including the objectives with respect to safety requirements set out in Directive 2014/35/EU, but with no voltage limit applying;

 It is informative at this point to also point out that both the R&TTE 1999/5/EC and the RED 2014/53/EU exclude the Low Voltage Directive from being applicable to the equipment if either R&TTE or RED are applicable.

See below an excerpt from recital (46) from the R&TTE Directive 1999/5/EC:

…whereas Directives 73/23/EEC and 89/336/EEC will no longer apply to apparatus within the scope of this Directive, with the exception of protection and safety requirements and certain conformity assessment procedures,

And also see below recital (7) from the RED 2014/53/EU:

(7) The objectives with respect to safety requirements laid down in Directive 2014/35/EU are sufficient to cover radio equipment, and should therefore be the reference and made applicable by virtue of this Directive. In order to avoid unnecessary duplications of provisions other than those concerning such requirements, Directive 2014/35/EU should not apply to radio equipment.

 This can be confusing unless you read it a few times. What it means, in the cases of both the R&TTE Directive 1999/5/EC and the RED 2014/53/EU, is this:

  1. Annex I from the Low Voltage Directive is applicable to equipment within the scope of either “radio” Directives regardless of the power input. Therefore if your device has a tiny coin cell battery and a wireless module and no connection to AC mains power you must comply with Annex I of the LVD.
  1. In these cases only Annex I from the LVD is applicable and nothing else from the LVD.
  1. The LVD will not be referenced on the EU declaration of conformity for the product because compliance with Annex I of the LVD is presumed when compliance to either R&TTE or RED are claimed. Therefore the LVD itself is excluded, only Annex I is applicable and that is through Article 3 (1.) (a) of both the R&TTE Directive 1999/5/EC and the RED 2014/53/EU.

So, the next question is, “What is Annex I of the LVD?” See below:


Compliance with Annex I of the LVD will require, in most cases, testing using an applicable harmonized EN standard from the official list published in the Official Journal of the European Union. The latest available list was published on July 8, 2016 and is published here: LVD standards OJ List.

F2 Labs is here to help. Have a question or a comment? We can be contacted via this link. We can be reached by phone at 877-405-1580 and are here to help you.

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

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:

The option for the appointing of an Authorized Representative is made available in all of the above indicated CE marking Directives, but it is not the same for each, and whether or not it is required can also be dependent upon the compliance path of the product. We will investigate and summarize these requirements for the above EU laws in the following article.

Machinery Directive 2006/42/EC

The Machinery Directive (MD) 2006/42/EC defines what an authorized representative is as it pertains to the Machinery Directive in Article 2 (j): ‘authorised representative’ means any natural or legal person established in the Community who has received a written mandate from the manufacturer to perform on his behalf all or part of the obligations and formalities connected with this Directive;

That is pretty broad. Essentially, it means that an Authorized Representative can be assigned all or some of the duties, as applicable. For the Machinery Directive, you could appoint someone to handle the whole compliance process, just a small part of it, or anything in between. An important note is that there must be a written mandate (legal agreement) between the parties.

Low Voltage Directive 2014/35/EU

The Low Voltage Directive (LVD) 2014/35/EU, Article 1 (4) indicates the definition:

(4) ‘authorised representative’ means any natural or legal person established within the Union who has received a written mandate from a manufacturer to act on his behalf in relation to specified tasks;

Note that the definition in the LVD is not as broad. The definition includes ‘specified tasks’ and not ‘all or part’ as in the MD.

Next we move to Article 7 of the LVD which addresses specifically the role of the Authorized Representative as it pertains to the Low Voltage Directive.


Immediately we see that Article 6 (1) is referenced. That is below:


It is worth noting that Article 3 and Annex I are the requirements for the manufacturer in the LVD to make the product safe for use, i.e., the testing and evaluation.

Additionally, the technical file is referenced in Article 7 and explicitly states that the Authorized Representative cannot be responsible for compiling that, but can be the holder of the Technical File. This layer of separation between the compliance responsibilities (that may be assigned) as an LVD Authorized Representative is in contrast to the myriad of duties assignable as an MD Authorized Representative. To highlight this, attention should now be drawn to the minimum duties for an LVD Authorized Representative. For that see (above) Article 7 (2.) – (a), (b), & (c).

Annex III of the LVD is the sole conformity route available to LVD products. Annex III (4) shows the requirement for a CE marking and the EU declaration of conformity:


You may add these responsibilities to the Authorized Representative mandate, if you choose, by way of Annex III (5):


Electromagnetic Compatibility Directive 2014/30/EU

The Electromagnetic Compatibility Directive (EMCD) 2014/30/EU also allows the use of an Authorized Representative and since the EMCD, like the LVD, is a New Legislative Framework Directive the definition and duties of an Authorized Representative are the same. The New Legislative Framework of 2008, or “NLF” as it is referred, is the collection of a number of Directives that were written in order to streamline the responsibilities that overlap among the various Directives it encompasses. The responsibilities of an Authorized Representative under the LVD and EMCD (and others) are an example of this. Article 7 in the LVD is repeated perfectly as Article 7 in the EMCD.

The EMCD, unlike the LVD, does have mechanisms for the involvement of a Notified Body in the additional conformity modules besides Module A, Internal Production Control. The other conformity modules are indicated in Annex III, Part A, Module B, EU-type examination and Module C: conformity to type based on internal production control. These two additional conformity modules, unavailable in the LVD, allow for the interface of the appointed Authorized Representative with a Notified Body who may be involved in the EMCD compliance process by lodging the application with the Notified Body on behalf of the manufacturer.

ATEX Directive 2014/34/EU

The Equipment and Protective Systems intended for use in Potentially Explosives Atmosphere Directive (ATEX) 2014/34/EU follows the same path as the EMCD previously referred to.

Regarding ATEX, the European commission has published a complimentary document, the purpose of which is to elaborate, in plain English, the intent of the requirements listed in the ATEX Directive 2014/34/EU. The link for this document is here (it is a direct download link) and it is a free download, like all of the European Commission documents pertaining to CE marking. The document is titled ATEX 2014/34 EU Guidelines and section 3.5, below, elaborates on the role of the Authorized Representative.


Note that there is another paragraph to section 3.5 which is not pasted above. That paragraph deals with the role of the Authorized Representative responsibilities for equipment already in the EU and having used the expired ATEX Directive 94/9/EC instead of 2014/34/EU. This will not be discussed in this article.

Radio Equipment Directive 2014/53/EU

The Radio Equipment Directive (RED) 2014/53/EU follows the same path as the EMCD ATEX Directive previously referred to.

Medical Device Directive 93/42/EEC

The Medical Devices Directive (MDD) 93/42/EEC has perhaps the most requirements and responsibilities as compared to the other Directives referenced in this article. A manufacturer of medical devices, with the intention of making their products available in the EU, should also read and understand the very comprehensive overhaul of the MDD with the amendment to the MDD in Directive 2007/47/EU. The MDD makes requirements for the involvement of an Authorized Representative and the amendment elaborates on these roles and adds more. See below for further explanation.

There are twenty mentions of the term “authorised representative” in Directive 2007/47/EC. This article will focus on the most important aspects of the amended requirements.

First, we note that the installation of a required Authorized Representative for manufacturers without a physical EU footprint is now codified in the MDD by the addition of recital (14), below.


The definition of Authorized Representative, as pertains to the MDD, is added to Article 1 (2.) (j).


Article 10 (a) (2.) mandates the requirement for an Authorized Representative, physically located in the EU when the manufacturer does not have an office or location in the EU.


The MDD 93/42/EC, Article 14 paragraph two, displayed below…



…is replaced by this section from the new Directive 2007/47/EC.


To sum this article up, please see the below bulleted points.

  • The MD does not require an Authorized Representative but you may appoint one to handle some of the duties, some of which may be difficult to satisfy. For instance, the requirement for a European address on the declaration of conformity.
  • The LVD, EMCD, ATEX, and RED do not require an Authorized Representative but if you assign one there is a minimum list of required duties that must be ascribed.
  • The MDD requires an Authorized Representative if you are putting your products in the EU but do not have a physical location in the EU.
  • All Authorized Representatives, for assistance in meeting compliance requirements for any of the aforementioned CE marking Directives, will require a written mandate or agreement in place that designates duties and responsibilities.

F2 Labs is here to help. Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.





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

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 period for the RED so until June 2017 you can choose an appropriate compliance path, or compliance module, from either Directive. There are a few changes with the new Directive that will be discussed in this article.


First, let’s define the type of equipment that is within the scope of both Directives.

The scope and definitions of the R&TTE Directive 1999/5/EC is below.

R&TTE 1999/5/EC, Article 1 (Scope and Aim) (1.)

  • This Directive establishes a regulatory framework for the placing on the market, free movement and putting into service in the Community of radio equipment and telecommunications terminal equipment

R&TTE 1999/5/EC, Article 2 (Definitions) (b) & (c)

(b) ‘telecommunications terminal equipment’ means a product enabling communication or a relevant component thereof which is intended to be connected directly or indirectly by any means whatsoever to interfaces of public telecommunications networks (that is to say, telecommunications networks used wholly or partly for the provision of publicly available telecommunications services);

(c) ‘radio equipment’ means a product, or relevant component thereof, capable of communication by means of the emission and/or reception of radio waves utilising the spectrum allocated to terrestrial/ space radiocommunication;

Radio Equipment Directive 2014/53/EU, Article 1 (Subject matter and scope) (1.)

  • This Directive establishes a regulatory framework for the making available on the market and putting into service in the Union of radio equipment.

Radio Equipment Directive 2014/53/EU, Article 2 (Definitions)

(1) ‘radio equipment’ means an electrical or electronic product, which intentionally emits and/or receives radio waves for the purpose of radio communication and/or radiodetermination, or an electrical or electronic product which must be completed with an accessory, such as antenna, so as to intentionally emit and/or receive radio waves for the purpose of radio communication and/or radiodetermination;

From the outset, as demonstrated above, we can see that the R&TTE Directive covers radio equipment and telecommunications terminal equipment (read that as “wired”) while the RED us for radio equipment, only. There are three other ‘major differences’, please read on.

The second big difference between the R&TTE is the lowering of the frequency limit. The R&TTE applied to radio equipment from 9 kHz to 3,000 GHz (see 1999/95/EC, Article 2 (d)) while the RED applies to radio equipment operating below 3,000 GHz (see 2014/53/EU, Article 2 (1. (3)).

Thirdly, the R&TTE Directive allowed the manufacturer to choose to comply with either the R&TTE Directive or the Low Voltage Directive and the EMC Directive, as long as the radio module used in the device was suitably approved to the R&TTE Directive (see Article 10 (2.)). What this means is that if your product incorporated a wireless module that was already tested, evaluated, found to be compliant, and had a CE marking with a claim to the R&TTE Directive then you could follow the conformity modules available in the Low Voltage Directive and the EMC Directive instead of the R&TTE Directive for the overall apparatus. This option is not available in the RED.

Finally, the RED has a new requirement for the registration of products that fall into a product type that is commonly non-compliant. See Article 5 below.


There are other changes and some differences not addressed in this article. Many are the same changes in the other NLF Directives. Another is the introduction of the simplified EU declaration of conformity. We will publish more articles regarding the new Radio Equipment Directive 2014/53/EU in the future and will discuss more changes brought in with the Radio Equipment Directive 2014/53/EU and others.

Before I close this article I want to discuss one more issue regarding the RED. That issue is the use of harmonized EN standards for the proof of compliance to the Directive. For now (as of September 15, 2016) there are only eight official, harmonized EN standards for proving compliance to the RED. By ‘official’ I mean they were published in the Official Journal of the European Union. That list is here: RED harmonized EN standards.

There are a number of harmonized EN standards that are applicable to the R&TTE Directive. The official list is here: R&TTE harmonized EN standards. We suggest you bookmark that link because the list has been removed and from the official European Commission  page for radio equipment. The R&TTE Directive is three months into its 12-month final tour and so the EU has removed reference to the R&TTE standards and replaced it with the list of eight RED standards. This is important because between now (September 2016) and the end (June 2017) the guidance we have received from the EU RED Notified Body we partner with for EU-type examinations (the formal review process for technical documentation and reports that is required for some radio products) is that you are able to use either the R&TTE standards or the RED standards to prove compliance to the RED. It is expected that the official RED list will be populated with most or all of the R&TTE standards by next June anyway.

F2 Labs is here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.


Posted in CE marking, R&TTE Directive 1999/5/EC, Radio Equipment Directive 2014/53/EU | Tagged , , , , , , , , , , , , , , , , , , , | Leave a comment

CE markings, Ex markings, and other EU markings claiming product compliance

ce_1st pic

Manufacturers who build equipment for sale to customers in the European Union may spend a lot of time learning about and understanding the process that is required in order to sell their products with a CE marking on it.

Placing a CE marking on your equipment is your claim to the European Union that your product complies with any applicable CE marking Directive. This is an important point because there are many CE marking Directives and any that are applicable (meaning: your product is covered under their scope(s)) must be addressed and complied with. Neglecting to comply with a CE marking Directive because you did not know it is applicable to your product does not reduce or negate your obligations.

A list of CE marking Directives for which we provide technical and consultative support is below:

Radio & Telecommunications Terminal Equipment Directive 1999/5/EC


There are many EU Directives and regulations that, although look like CE marking Directives, are not CE marking Directives. These may be laws and they must be complied with but they are not attached to your CE marking. The difference is that the non-CE marking Directives and Regulations make no mention or reference to the CE marking or the declaration of conformity. Some examples are below:

The WEEE Directive has its own mark:


And so does Regulation (EC) 1935/2004:


The General Product Safety Directive 2001/95/EC has no mark and compliance to it is not indicated by CE marking. It is implied simply by placing your product on the market in any of the EU member nations.

To top the above three examples, the ATEX Directive 2014/34/EU requires a CE marking and an Ex mark:


The Ex mark is interesting because it is a mark that is required in addition to the CE marking. We do not see that in other CE marking Directives. The Ex mark is mentioned throughout the ATEX Directive 2014/34/EU.

Notably, see 2014/34/EU, Article 6, Obligations of manufacturers, (6.)


See also 2014/34/EU, Article 38 (abbreviated), Formal non-compliance, (1.) (c)


Finally, we see the requirement stated in 2014/34/EU, Annex II (1.0.5.) (6th indent)


The Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU is a CE marking Directive. This means that only the CE marking is recognized as showing that the product is in compliance with the RoHS Directive. Furthermore, if your product is within the scope of the RoHS Directive and you place a CE marking on it then that means that you are claiming that your product complies with the RoHS Directive 2011/65/EU – even if you did not even know that your product is within its scope.

See below RoHS 2011/65/EU, Article 16 (1.)


The CE marking is the only marking that is the legal representation of RoHS compliance for your product. It’s interesting to perform a Google image search for “RoHS marking”:


None of those RoHS markings mean anything legally. The EU RoHS markings are the result of marketing, drawn up by an artist and put on a product to convey RoHS compliance but they are not legal marks. Some of the other markings convey Chinese RoHS compliance, which is not related to EU RoHS compliance in any way.

The staff at F2 Labs can help you sort out these requirements, the markings you will need, and how to perform the necessary testing and evaluation required prior to the application of the correct markings.

We are here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.


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 | Leave a comment

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 means that you have to check, once in a while, to make sure that the product you are sending to the EU was tested and evaluated using the current, relevant EN standards and claim compliance to the current Directive(s).  F2 Labs suggests that you check the status of your CE marking Directives and EN standards at least once per quarter if you are actively shipping products to the EU. We will show you how in this article.

There are two parts to the compliance of your product when you get it ready for the CE marking. The first is to determine which CE marking Directive(s) is (are) applicable. You must comply with whatever laws (CE marking Directives) apply to your product. The second part is to determine which standards you will use to prove that your product complies with the law(s). In other words: you comply with the Directives using the EN standards.

This means that you really need to check two things regarding the compliance of your product, from time to time, if you sell to the EU in an ongoing basis.

  1. The status of the CE marking Directives. These are the laws. They change from time to time.
  2. The status of EN standards. These are the technical requirements and testing used to prove compliance to the CE marking Directives. They also change periodically.

Fortunately, the EU puts this information at your fingertips on the world wide web. In this article we are going to work towards checking the status of EN ISO 13849-1, which was recently updated and replaced by a newer version of itself and we will detail how this will impact your project.

The European Commission has a page for all of the CE marking Directives. The page for the Machinery Directive 2006/42/EC is at this link. Looking at this page we first see the chart in the middle of the page which gives us some basic information about the Machinery Directive and some useful links.


Scrolling down the page, we then get to the list of harmonized standards.  Before we look at this list let’s discuss the role of harmonized standards and your project….

Let’s take a quick time-out to ask and answer a very common question –

  • Question: “What does the term “harmonized standard” mean?”
  • Answer: Harmonized standards are the standards that have special status in that they confer, “presumption of conformity,” to products to which they are applied when used to prove that a product complies with a CE marking Directive to which they are harmonized (meaning, officially connected or attached).

…In other words, before you place a CE marking on your product it must be in compliance with any applicable CE marking Directives and in order to do so you need to show that you have selected appropriate harmonized EN standards and tested/ evaluated your product according to those standards.

Yes, the standards are voluntary, but they usually provide the quickest route to compliance. Any deviation from the application of a harmonized standard during the compliance process for machinery will require a full risk assessment for each Annex I Essential Health and Safety Requirement not covered by the applicable standard. The standards route is the way to go if possible.

Continuing, let’s take a look at the next part of the European Commission’s Machinery Directive page, the display of the harmonized EN standards.


The link at the top of that screen-grab is to the official list of harmonized EN standards for the Machinery Directive. The list that follows (not in the above view) is taken from the linked list but only the list at that link is the ‘official’ list. I want to note that because sometimes, rarely, the list on the European Commission page we are discussing in this article is not identical to the official list. In order to get on the official list, and then published to the European Commission’s Machinery Directive page, it must first be published in the Official Journal of the European Union.

Below is the start of the list on the European Commission page. This is the page we at F2 Labs refer to for direction when selecting harmonized EN standards for consideration by our customers for their EU projects.


Let’s take a very close look at this chart so we can understand the information that it is giving to us. First, notice the reference to ESO. This is for the European Standards Organization responsible for making the standard a ‘harmonized’ standard. Frequently these standards are taken from the IEC or ISO. Usually the standards are the same as the IEC or ISO versions – but many times they are not. This is why you must reference to the EN version of the standard. EN 60204-1 is not the same as IEC 60204-1, for the purposes of CE marking. The EU has committees of engineers who decide on the standards and these groups are CEN and CENELEC.

Moving right across the chart we see the reference to the particular standard. There are many, many standards on this list and the task for you or, better yet, your accredited 3rd party testing organization (for instance, F2 Labs) is to select the standards from this list that are applicable to your product and help to prove that the product complies with the Essential Health and Safety Requirements from Annex I of the Machinery Directive.

Next we see the reference to the first publication date and then the superseded standard, and finally the date of cessation of presumption of conformity for the superseded standard. These dates cause a lot of confusion, all the time.

Looking at EN ISO 12100:2010 we see that it was first published on April 8, 2011 (note: in the EU the month is listed second when looking at a date in the format dd/mm/yyyy). April 4, 2011 was the date that this standard was officially unveiled to the world as an acceptable standard to use for risk assessment for products falling within the scope of the Machinery Directive.

Then we see three other standards: EN ISO 12100-1:2003, EN ISO 12100-2:2003, and EN ISO 14121-1:2007. Looking to the right of those standards we see a date of November 30, 2013. That date, November 30, 2013, is the date at which a product could no longer claim compliance using those three standards. From that date forward only EN ISO 12100-1:2010 could be used as the risk assessment standard.

So, from April 4, 2011 until November 30, 2013 you could use either EN ISO 12100-1:2010 or EN ISO 12100-1:2003, EN ISO 12100-2:2003, and EN ISO 14121-1:2007 for the risk assessment for your machine. Starting on November 30, 2013 only EN ISO 12100-1:2010 was acceptable.

You may be asking yourself this after reading the above: “How does this affect my product if I used a third party (like F2 Labs) to test and evaluate a machine I built in 2012 and started shipping to the EU, and I am still shipping it to the EU?

That is a good question and the purpose for this article. Let’s say you manufacture a machine and have a few orders per year for the EU. Chances are your machine will be within the scope of EN ISO 13849-1, which is a B-type Machinery Directive 2006/42/EC EN standard. (B-type standards are, “family standards,” meaning they are likely applicable to a wide-range of products.)

See EN ISO 13849-1 as displayed currently on the previously referenced Machinery Directive site:


EN ISO 13849-1 is a standard for control systems on machines – it is applicable to most types of machinery. Notice that it is also an ISO standard, ISO 13849-1. Note that for European projects you must reference the European version, EN ISO 13849-1.

Looking at the above graphic we see that there is a new version of the standard: EN ISO 13849-1:2015. Moving right, we can see that it replaced EN ISO 13849-1:2008, and the date of cessation of presumption of conformity for EN ISO 13849-1:2008 was on June 30, 2016.

Understanding what was written previously in this article we know that means that European machinery designed and evaluated using EN ISO 13849-1, could use EN ISO 13849-1:2008 until June 30, 2016. Starting on that date you must show that your machines complied with EN ISO 13849-1:2015. Therefore, on your declarations of conformity you must reference the 2015 version of the standard, if you used it, for shipments on or after June 30, 2016.

Just as important, you must be able to prove that you used that standard. It is not enough to list the correct standards. Behind the declaration of conformity, you should have a compiled Technical File to be able to prove to the European Authorities that your product actually complies with the current, relevant standards. Otherwise your product does not comply with the Directive.

The Technical File is your proof that the machine was actually compliant with the applicable CE marking Directives at the time you sent it to the EU. Further, you must be able to compile it and send it to the authorities, upon request, for ten years after you ship. Following is Annex VII from the Machinery Directive 2006/42/EC which is the Annex for the Technical File. Note in particular the highlighted sections.


Without application and compliance with the relevant, current, harmonized EN standards your machine is not in compliance with the Directive – and that means that technically you are breaking the law.

How can this impact me? Good question. Let’s take a look at a hypothetical situation that can show the ramifications for taking short cuts.

Widget Machine Company builds an industrial press and sells it to a company in France. The French company uses it for seven years and then decides to upgrade its machine. In order to fund the purchase of the new machine they sell the Widget Machine Company industrial press and use an auction company to do it. The auctioneer sells it to a Romanian company and the machine is shipped to Romania from France.

No translations are performed on any of the manuals from French to Romanian and after a few weeks a worker decides to service the machine for some issue. He removes a guard and cannot figure out how to reattach it. The next shift starts, the guard is on the floor next to the machine, and a new worker crushes part of his hand. The authorities will be involved and will make contact with Widget Machine Company to make a request for the Technical File. This will come by court order.

It is at this point you will either be glad you followed the correct procedure, used the right standards, and put your Technical File together at the time you built the machine and kept it updated or you will be looking for a lawyer to represent you in a European court.

A quick search of the Official Journal of the European Union yields many examples of court cases involving companies that did not follow the correct procedure or were unable to prove that they did.


Looking at the first case in that list (there are many, many more), we see it is titled Commission Implementing Decision (EU) 2015/1377. Opening that document and reviewing it tells us that a company in Sweden manufactured and sold log splitting equipment. It somehow came to the attention of the authorities and now the company is barred from placing a CE marking on the equipment… and barred from the entire EU.

Making sure that your equipment is appropriately compliant with the current Directives by using currently applicable harmonized EN standards will prevent this.

F2 Labs is here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.


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

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. Really, that is the point of the NLF: to make it easier for manufacturers to sell in Europe. The RED replaces the R&TTE Directive for equipment with radio communication ability and the new Directive offers an easier way to show compliance as pertains to the declaration of conformity.

In the other technical Directives we work with on a daily basis, there was no major change to the format or structure of the document. The RED is different because of the introduction of the simplified EU declaration of conformity.

A ‘simplified’ EU declaration of conformity? What is that?

To answer that question, let’s use the opportunity to briefly explain the concept of the declaration of conformity and what it is. A declaration of conformity is what sets the CE marking Directive apart from all other Directives, Regulations, and Decisions we see when understanding what our clients must do to send their products to the EU.

Broadly, if the Directive requires a CE marking, then it also requires that the product has a declaration of conformity. On the other hand, if an applicable Directive requires that the manufacturer must compile a declaration of conformity, then it will also make a requirement for a CE marking. They go hand-in-hand.

So, what is a declaration of conformity? A declaration of conformity is a one-page (usually) document that indicates at a minimum the name and address of the manufacturer, product information (model, description, serial number or range of serial numbers), the Directives complied with, the EN standards applied to prove conformity, and a sentence declaring sole responsibility by the manufacturer for the compliance of the product.

There is no mystery or magic to the declaration of conformity. The manufacturer even has a simple list to refer to in the Directive. See the RED 2014/53/EU, Annex VI.


Please note that there is no place for a 3rd party lab to sign or stamp the EU declaration of conformity. There is instruction regarding indicating that a Notified Body has been involved, however, in those cases it would be unlikely that the 3rd party test lab would be the same as the Notified Body because of the inherent of conflict of interest. Indeed, involvement by a Notified Body is as much a check on the manufacturer as it is on the technical intervention of the test lab.

Looking at the document, it seems simple enough and if you were making only a handful of products it would be pretty simple to draft a declaration of conformity each time you make a product or a handful of products. But, what if you make a bunch of products and in high quantities? It might be more challenging to draft and sign the documents in those cases.

The simplified EU declaration of conformity can make that easier. In the RED 2014/53/EU we first see the mention of it in recital (31).


It is mentioned again in Article 10 (9) and provides the instruction that it can be referred to by internet address.


And, finally, we see in Annex VII it is listed on its own.


This allows for a manufacturer to ease the compliance burden for a product by putting the declaration of conformity on the web, instead of printing it in a manual.  Additionally, we note that you can indicate a range of serial numbers on a single declaration of conformity. That means you can indicate, using one web address, the sole declaration of conformity to prove compliance for an unlimited number of products to which the declaration of conformity applies – and you can update the document to indicate new serial numbers and even new compliance methods (for instance new testing if a standard is revised, etc.).

I want to note that although I have known about the simplified declaration of conformity for two years it was not until I read a similar requirement in the new PPE Regulation (EU) 2016/425, recital (24) that I decided to point this new trend out in a blog article.


You may consider it a good idea to adopt the simplified EU declaration of conformity format, even for products that don’t require it (for instance, medical devices, or products under the Low Voltage Directive) because it could ease the overall burden of keeping the document in order: One document in one place.

F2 Labs is here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.

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

What is IP testing?

At F2 Labs, our IP testing chambers are constantly filled with projects undergoing testing to IEC 60529. Since I work in the sales department at F2 Labs I field a lot of questions, every day, about IP testing, what it is, what we look for after the testing, and how the ratings work. This article will focus on these topics.

IP stands for ingress protection and tests the ability of your product to withstand everything from finger tips to a high pressure jet of high temperature water. The testing is by enclosure and your product does not have to be populated with the electronics in order to undergo the testing. However, it can be populated and we can test the functionality of the product, before and after the testing, by request.

You have probably noticed that there are two numbers usually displayed in an IP rating, for instance: IP65. The first number is for the ingress of solid foreign objects. This can be anything from finger tips to dust in a chamber. The second number is the water test.

The tests corresponding to the individual ratings for solid foreign objects are below.

Solid Foreign Objects

IP1X – objects ≥ 50mm
IP2X – objects ≥ 12mm
IP3X – objects ≥ 2.5mm
IP4X – objects ≥ 1mm
IP5X – dust protected
IP6X – dust tight

I walked out to our lab and took a photograph of our IP probes for the IP1X – IP4X tests.

Please see below, from left to right, IP4X, IP3X, IP2X, IP1X.

ip probes

IP5X and IP6X are different tests and require a higher degree of protection for your enclosure. Both ratings involve your product being placed in an airtight chamber and then subjected to circulating dust (talcum powder) blown over and on the product for hours. That is where the similarity stops.

The IP5X test may or may not require the installation of a vacuum barb. That is determined by the category in which your product falls. Category 1 enclosures do  require a barb while category 2 enclosures do not require an installed barb for the IP5X test. The purpose of the barb is for the lab technician to connect an air hose to your product. That air hose is connected to a vacuum pump on the other end, outside the chamber, and we will try to draw air into the enclosure, pulling dust with it. Dust may enter the enclosure during the IP5X test but in order to pass there may be no dust on any conductive surface.

How are the categories defined? Category 1 enclosures are enclosures which may heat up during operation (for example: if electronic components are inside). Category 2 enclosures do not experience a temperature change.

I mentioned above that the similarity between the IP 5X and IP6X testing stopped at the dust chamber. That is because the IP6X test requires a vacuum barb and makes no distinction between category 1 or 2. Most importantly, the IP6X test allows for no dust to enter the enclosure. Simply, if dust is visible anywhere in the enclosure at the conclusion of the testing the product fails.

Before we proceed I want to show a picture of a vacuum barb because while everyone knows what they are my experience is that people refer to them differently.


Many times I will discuss the vacuum barb issue with the customer and the need to install it. The standard calls for it if your product is an IP5X category 1 enclosure and any time you want an IP6X test. We are an A2LA accredited lab and follow the standard, directly. The test sample must come to us with the barb installed unless previously agreed upon. We can install the barb in your product for an additional fee but it is best for the manufacturer to provide the test sample to us in a state that is ready to immediately undergo the testing.

The second part of the testing is for the intrusion of water. The passing criteria for the water test is the same for all nine water tests: broadly, no water can settle on any conductive surfaces. We carefully open the product following the testing and take clear photographs throughout. We will see if water has entered your enclosure and determine the impact to your product. Our techs are extremely careful when opening the product because water can settle at the bottom and unless there are live wires or boards at the bottom, in water, your product may still pass the testing.


IPX1 – Vertically dripping water
IPX2 – 75° to 90° dripping water
IPX3 – Sprayed water
IPX4 – Splashed water
IPX5 – Water jets
IPX6 – Powerful water jets
IPX7 – Effects of immersion
IP8 – Immersion, by agreement, must be more strenuous than IPX7
IPX9 – Increasing high pressure, high temperature water jetting

The tests listed above are self-explanatory but the IPX7, IPX8, and IPX9 testing merit further discussion.

IPX7 calls for your product to be immersed in a water tank for 30 minutes. The depth depends upon the enclosure size. Enclosures with a height less than 850 mm must have the lowest point of the enclosure 1,000 mm below the surface. For enclosures with a height equal to or greater than 850 mm the top of the enclosure must be 150 mm below the water surface. Note that the enclosure is measured in its working position and is situated in the tank in its working position as well.

The IPX8 test is the same as the IPX7 test except the depth and or duration of the testing is by agreement between the manufacturer and the testing laboratory. The testing must be more severe than the IPX7 testing. For instance, an IPX8 test for an enclosure may be for 35 minutes instead of 30 minutes and the depth may be the same as is called for in the IPX7 test. Or, the testing may be for 30 minutes but the depth for a product that is less than 850 mm may be 1,050 mm during the testing. We have performed testing at greater depths and for much longer periods of time. Let us know what you want – we creatively determine solutions on a daily basis.

IPX9 testing is the most strenuous of all. It requires that your product is sprayed with a high pressure stream of water (8,000 to 10,000 kPa) heated to 80° C. This testing is done at multiple angles (30 second dwell per position) on a turn table in our water chamber.

One question which is frequently asked by new customers is whether or not each test must be passed in succession in order to achieve a rating. For instance, to attain IP65 status does the product need to pass IP1X, IP2X, IP3X, IP4X, IP5X, IPX1, IPX2, IPX3, IPX4? The answer is no. In fact, passing IP65 allows the claim of all IP ratings below IP65. This question then, many times, leads to a discussion regarding how to plan this testing, since the manufacturer may not be confident regarding the ability of the product to pass. Some manufacturers ask us to start with lower tests and work up to the desired rating while others work from the toughest test and down. This is the decision of the manufacturer.

I hope this article has been helpful and we are at your service if you have additional questions or want to schedule IEC 60529 IP testing for your products.

F2 Labs is here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.

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FCC Labeling Requirements


Recently the F2 Labs sales department was presented with a question from a call-in customer who wanted to know about the requirements from the FCC to label equipment. Specifically, she asked about e-labelling. She relayed that the FCC’s rules regarding this are not very clear.

You can read the FCC’s E-Label guidance here – Link – or you can do what we did – we asked F2 Labs’ Director of EMC & Wireless Operations and then read his response (below):

Here are the rules from the FCC:

(d) In order to validate the grant of equipment authorization, the nameplate or label shall be permanently affixed to the equipment and shall be readily visible to the purchaser at the time of purchase.

(1) As used here, permanently affixed means that the required nameplate data is etched, engraved, stamped, indelibly printed, or otherwise permanently marked on a permanently attached part of the equipment enclosure. Alternatively, the required information may be permanently marked on a nameplate of metal, plastic, or other material fastened to the equipment enclosure by welding, riveting, etc., or with a permanent adhesive. Such a nameplate must be able to last the expected lifetime of the equipment in the environment in which the equipment will be operated and must not be readily detachable.

(2) As used here, readily visible means that the nameplate or nameplate data must be visible from the outside of the equipment enclosure. It is preferable that it be visible at all times during normal installation or use, but this is not a prerequisite for grant of equipment authorization.

(e) A software defined radio may be equipped with a means such as a user display screen to display the FCC identification number normally contained in the nameplate or label. The information must be readily accessible, and the user manual must describe how to access the electronic display.

So in order for the display screen clause to be used, it has to be a software defined radio, and it must be on the actual equipment and not show up on the cell phone that is accessing it.

Subsequently I asked him if I could have the link to this rule on the FCC website. Below is the link

FCC Rule 2.925 (d)

This question is one of the reasons we started our blog. There are so many rules for manufacturers that identifying what your responsibilities are as pertains to the many rules that could apply can be a daunting task. We are making an effort to note some of these questions and offer guidance on our blog.

F2 Labs is here to help.

Have a question or a comment? We can be contacted via this link. We can be reached by phone at 855-652-7281 and are here to help you.

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