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Ask Your QuestionFrequently Asked Questions
Which products are not regarded as EEE (Electrical Electronic Equipment) in the scope of the RoHS Directive 2011/65/EU?
Check the list of products that do NOT fall within the scope of the RoHS Directive 2011/65/EU.
What is the significance of 014/003/002 etc. in the ATEX 014 X certificate number?
Typically, EU Type Certificates such as ATEX certificates which are issued by a notified body contain a reference number which relate to an internal reference and/or test report which is correlated to that specific certificate.
Which are the current CE marking Directives and Regulations?
Seize the opportunity and gain an in-depth overview of the scopes of the applicable EU Directives and Regulations and contact us with any request.
Is CE a quality mark?
A CE marking is not regarded as a quality mark. but it is often referred to as a CE quality mark.
Who is responsible for testing the CE marking?
Stating that a CE marking will be tested, is not correct. The CE marking is affixed to a product (by the manufacturer).
Latest questions
What is the significance of 014/003/002 etc. in the ATEX 014 X certificate number?
Typically, EU Type Certificates such as ATEX certificates which are issued by a notified body contain a reference number which relate to an internal reference and/or test report which is correlated to that specific certificate.
Which are the current CE marking Directives and Regulations?
Seize the opportunity and gain an in-depth overview of the scopes of the applicable EU Directives and Regulations and contact us with any request.
What is the risk class of my medical device?
Medical devices are divided into four categories or classes, from the lowest to the highest risk class: I*, IIa, IIb and III. The higher the risk for the patient/end-user, the higher the risk category. Read more about the classes of the medical devices and the changes as of May 2021.