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Which are the current CE marking Directives and Regulations?

What is the risk class of my medical device?

In which countries is it required to affix a CE marking?

When is CE marking required?

How much does CE certification cost?

Is CE a quality mark?

On which part of the medical device must the CE marking be affixed?

Who is responsible for affixing the CE marking?

Is a CE marking mandatory?

Who carries out the CE approval process?

What is a CE standard?

How can I apply for CE certification?

Where can I apply for a CE marking for machinery and installations?

What is an EC Marking?

Who is responsible for testing the CE marking?

Who is responsible for the CE marking of machinery and installations?

Which institute issues the CE marking?

Where to find the CE requirements for a User Manual?

Which products are not regarded as EEE (Electrical Electronic Equipment) in the scope of the RoHS Directive 2011/65/EU?

Which products are considered EEE within the scope of the RoHS Directive 2011/65/EU?