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Frequently Asked Questions

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Frequently Asked Questions

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

Date: 15.10.2015

Check the list of products that do NOT fall within the scope of the RoHS Directive 2011/65/EU.


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What is the significance of 014/003/002 etc. in the ATEX 014 X certificate number?

Date: 10.02.2022
 (from Dinesh Kumar Pappula)

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.


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Which are the current CE marking Directives and Regulations?

Date: 24.07.2021

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.


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Is CE a quality mark?

Date: 15.05.2018

A CE marking is not regarded as a quality mark. but it is often referred to as a CE quality mark.


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Who is responsible for testing the CE marking?

Date: 10.12.2015

Stating that a CE marking will be tested, is not correct. The CE marking is affixed to a product (by the manufacturer).


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Latest questions

What is the significance of 014/003/002 etc. in the ATEX 014 X certificate number?

Date: 10.02.2022
 (from Dinesh Kumar Pappula)

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.


Read more

Which are the current CE marking Directives and Regulations?

Date: 24.07.2021

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.


Read more

What is the risk class of my medical device?

Date: 08.05.2021

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.


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