CE MarkingIt is a **European market safety certification**, regarded as a passport for manufacturers to enter the European market.CE represents Conformité Européenne (European Conformity)Products bearing the CE mark can be sold in all member states of the European Union without the need to comply with additional requirements.Each member state requires the CE certification, which is a mandatory certification in the EU.

CE MarkingBased on the product variations, certification categories differ, mainly including the following types:

Low-voltage products.This category mainly includes electrical and similar products, such as televisions, computers, ceramic valves, ballasts, and the like.
Electromagnetic Compatibility Products.Including residential environment equipment, power semiconductor converters, and household heating appliances.
Medical Device CE CertificationMedical devices used in the European healthcare system are subject to CE certification.Medical device certifications encompass the safety of the product itself as well as requirements for labeling, and also include related services such as installation, operation, adjustment, and maintenance of the medical devices.
Pressure Equipment CE CertificationMainly includes high-pressure pressure vessels, high-pressure boilers, medical equipment, fluid pipeline equipment, etc. Pressure equipment requires regular inspections and testing to ensure normal operation.。

In addition, there are CE certifications for toys, IT equipment, and more.The specific certification categories must be determined based on the type of product and the EU directive.