CE conformity assessment

We advise on all aspects of CE marking

Thanks to the European single market, companies can make their CE-marked products available in all EU countries (and even beyond). The manufacturer uses a conformity assessment procedure to ensure that it has complied with all necessary EU regulations and documents this in the EU Declaration of Conformity. This procedure is also required for products that are only used in your own company.

We will be happy to advise you on all CE marking issues and support you with legally compliant documentation.

5 steps to CE conformity

What we can offer you

Expert advice from certified CE coordinators
Conformity assessment according to current EU regulations
Search for applicable harmonized standards
Risk assessment according to EN ISO 12100
Preparation of the EU Declaration of Conformity ready for signature
Checking that regulations and standards are up to date
Fast processing of your declaration
Always up-to-date regulations and standards as a basis
If desired, acting as an authorized representative for representation before national authorities

Your contact at ED-Technik GmbH

Do you have any questions?
We are also happy to advise you personally by e-mail or telephone.

Martin Tillmann
Managing Director
Dipl.-Ing. Mechanical Engineering
DIN EN ISO / IEC 17024 certified expert for
CE conformity assessment and technical documentation

Our services in the field of CE conformity assessment

Classification of the product in the applicable EU directives
Research of the relevant harmonized standards
Product analysis, risk analysis, hazard analysis incl. Determination of the necessary measures before commissioning
Requirements for external and internal documentation
Coordination and implementation of required measurements
Preparation of the CE declaration (declaration of conformity, declaration of incorporation)
Compilation of external and internal technical documentation
Preparation of expert opinions and technical reports for conformity assessment

In addition, we offer to act as an“authorized representative” within the meaning of the “Blue Guide” (Chapter 3.2 Official Journal C 272).

We would then have to carry out the following (additional) tasks:

to keep the EU Declaration of Conformity and the technical documentation available for the national supervisory authorities and to cooperate with them on request;
at the reasoned request of a competent national authority, provide that authority with all the information and documentation necessary to demonstrate the conformity of a product;
cooperate with the competent national authorities, at their request, on any action taken to eliminate the risks posed by products falling within their remit.

Depending on the conformity assessment procedure and the relevant Union harmonization legislation, the authorized representative may also be designated for this purpose, for example,

affix the CE marking (and any other markings) and the number of the notified body to the product;
to draw up and sign the EU Declaration of Conformity.

Managing Director Dipl.-Ing. Martin Tillmann is a DIN EN ISO 17024 certified expert for CE conformity assessment

Our risk assessment tool

The TÜV-certified Safexpert software supports us with the following functions:

Standards Manager, which is automatically updated on an ongoing basis and checks projects for up-to-dateness.
Tabular assessment of risks, structured according to hazard class, hazard location and phase of life
Separate compilation of safety information for the user for inclusion in the instructions for use
Interface to Sistema, the IFA program for validating the performance level for functional safety in accordance with DIN EN ISO 13849-1 and DIN EN ISO 13849-2