1. The name and address of the manufacturer (EU authorized representative (EU authorized agent) AR), product name, model, etc.;

2. Product instruction manual;

3. Safety design documents (including key structural drawings, that is, design drawings that can reflect the creeping distance, gap, number of insulation layers and thickness);

4. Product technical conditions (or enterprise standards), establish technical data;

5. Product electrical schematic, block diagram and circuit diagram, etc.;

6. List of key components or raw materials (please select products with European certification marks);

7. Testing Report (Testing Report);

8. Relevant certificates issued by the EU authorized certification body NB (for models other than model A);

9. The product registration certificate in the EU (for some products such as: Class I medical devices, general IVD in vitro diagnostic medical devices);

10. CE Declaration of Conformity (DOC);