Application materials
1. The name and address of the manufacturer (EU authorized representative (EU authorized agent)), product name, model, etc .;
2. Product instruction manual;
3. Safety design documents (including key structural drawings, that is, design drawings that can reflect the climbing distance, clearance, number of insulation layers and thickness);
4. Product technical conditions (or enterprise standards), establish technical data;
5. Product electrical schematic diagram, block diagram and circuit diagram, etc .;
6. List of key components or raw materials (please choose products with European certification mark);
7. Testing Report;
8. Relevant certificates issued by the EU authorized certification body NB (for modes other than Mode A);
9. Registration certificate of the product within the EU (for some products such as Class I medical devices, general IVD in vitro diagnostic medical devices);
10. CE Declaration of Conformity (DOC);
