Often we get a question similar to this:
“Our product already has a UL and/or CSA approval. Does that mean that we automatically qualify for the CE marking?”
Unfortunately, that is not the case.
The CE marking requirements covers different aspects of a product’s design, production and distribution. Typically, various companies are involved in the design, manufacturing, distribution and placing on the market of products. The contributions of each single of these links in the production chain and distribution chain may affect the CE compliance of a product. For example, a product may be designed in accordance with the requirements, but may in the end not comply because during the production stage there was a deviation from the design. Or an electronic component may have been tested and approved for the requirements for electromagnetic interference, but can start to emit illegitimate disturbance when installed incorrectly. This raises the question of who is responsible for the CE marking.
Unfortunately, the process of determining whether the CE marking applies to a product is rather complex. The European legislator does not provide product lists or nomenclatures which indicate the appropriate CE marking directives.
The European CE certification procedure has been mainly set up to:
I have to admit it: I’ve used this lame joke. But I have heard other CE marking consultants use it on many occasions. In fact, I think it is one of the most used jokes in presentations about CE marking:
“What do the letters CE in CE marking stand for?”