The CE (Conformite Europeenne) mark is a safety certification mark and is regarded as a passport for manufacturers to open and enter the European market. CE-RED certification is referred to as Red certification (European wireless product certification), and the purpose is that wireless products in Europe must pass this test certification.

In the EU market, the CE mark is a compulsory certification mark. All products with the CE mark can be sold in the member states of the European Union (EU CE certification) without meeting the requirements of each member state, thus realizing the scope of the goods in the EU member states. free circulation within.

RED certified product range

TV and radio receivers, digital set-top boxes, network set-top boxes, digital satellite receiver top boxes, network signal receiver top boxes, network satellite receiver top boxes, and terrestrial receiver top boxes, all belonged to the scope of the EMC directive before, but now fall into the scope of the RED directive. Such as: AM/FM/ATV/DTV/DVB-T/DVB-S and other equipment that can realize radio and television signal reception fall into the scope of RED instructions, while DVB-C/CATV and other equipment that can only achieve their functions through cable are not. Included in the RED scope. Such as: CD/DVD/AUXIN and other non-wireless receiving functions do not belong to the RED directive.

EN62368 routine test items

1. Basic requirements (component structure, labeling and description, energy level, energy classification and protection, safety, explosion)

2. Injuries caused by electricity (electrical energy source protection, insulating structural materials and requirements, safety protection system components)

3. Electrical ignition (classification of power and potential ignition sources, safety protection, internal and external wiring)

4. Injury caused by harmful substances

5. Mechanical damage

6. Hot burning

7. Radiation (gradation of radiation energy sources, safety protection of laser technology radiation, safety of acoustic energy sources)

Information to be prepared for the EU RED Directive EN62368 test

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

2. Product instruction manual;

3. Safety design documents (including key structure design drawings of key structure layer spacing, clearance, quantity and thickness);

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

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

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

7. Test report;

8. Relevant professional certificates issued by the EU-authorized certification and testing agency NB (for other teaching modes other than Mode A);

9. Certificate of registration of the product in the European Union (applicable to certain products, such as Class I medical instruments, in vitro diagnostic medical instruments);

10. CE Declaration of Conformity (DOC).

EU RED directive EN62368 test processing process

1. Provide product specifications and operating instructions

2. The customer fills in the test application form and provides product information

3. Confirm testing standards; arrange baseline testing

4. Customer product rectification and testing arrangements

5. After the test is completed, organize the draft report

6. The customer confirms the report information, confirms "OK", and issues a sealed report

Please contact our company ZRLK for EU RED Directive EN62368 testing. We will provide you with professional and efficient testing and certification services with favorable prices and considerate service. If you provide us with product pictures and specifications, we will give you corresponding cycles, quotations and specific solutions according to your products. You are welcome to inquire!