Conformity Assessment according to the MDR

We are Authorized Body No. SKTC-113 and Notified Body No. 2265 for:

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices as amended.

For a better overview of how the conformity assessment process of medical devices takes place, you can consult the following chart: Flowchart of MD Conformity Assessment in NB2265.

In case of interest in our services in the field of Conformity Assessment of medical devices, please, send filled document "Questions for Quoting" on e-mail address stated in the form.

If you are interested in our services, please, contact our office.

Confirmation that we are authorised to perform the Conformity Assessment of Medical Devices in accordance with the mentioned regulation and the scope of activities can be found on official NANDO website.

One of the most important aspect of our work is independence, impartiality and objective assessment of evidence. Therefore NB2265 Top Management issued Declaration of impartiality which represents our commitment and best intention.

Download files

Questions for Quoting

DOC 184,50 kB

Minimal Requirements for Content of the Technical Files of MD according to the MDR

PDF 130,07 kB

General terms and conditions of 3EC International a.s. (GTC)

PDF 288,50 kB

Policy of CE marking use

PDF 40,77 kB

Pricelist for Conformity Assessment of MD

DOC 95,00 kB

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