Arazy Group

Medes Limited – EU: CE Authorized Representative – Arazy Group

If you want to know more about regulatory issues of Medical Devices, click here.

All Non-European manufacturers of medical equipment who wish to market their products in the EU market under their own name must designate a Regulatory Authorized Representative in order to meet CE requirements.

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Authorized Representative Services

In order to assist you, or to provide you a quote for our Authorized Representative services, please fill-in the following form:

The fields marked with asterisk (*) are mandatory

Contact Information

Name: *

E-Mail: *

Company Information

Company Name: *

Type: *

Country: *

URL: www. *

Telephone/Fax: *

Product Information

Please fill-in the following table to the best of your knowledge. Do not fill-in what you are not sure of. Feel free to add more information on the “free text zone” at the end of the form.

CE Product Name	Class	CE Marked	CE# †

† If the product is already CE marked please fill with the Notified Body number.

What do you need? (*)

AR services for already CE marked products

AR services and assistance in CE marking of Class I products

CE marking of new Class I products

Others

Additional Information

Free text zone

If you use Internet Explorer the free text zone might be restricted to 160 characters. Other navigators do not have this limitation. If you need to send us a longer text, please e-mail it to medes@arazygroup.com. Do not forget to mention your contact information in such e-mail. Thank you!