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CE stands for Conformité Européenne and means that a product conforms to any applicable European regulations for that product.

The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure. Please find below a list of the CE Marking Directives and regulations (European Union directives/regulations that require the affixing of a CE mark to the products covers by them)

Machinery Directive (MD) – 2006/42/EC
Low Voltage Directive (LVD) – 2014/35/EU
Electromagnetic Compatibility Directive (EMC) – 2014/30/EU
Toys Directive - 2009/48/EC
Simple Pressure-vessels Directive (SPVD) - 2014/29/EC
Medical Devices Directive (MDD) – 93/42/EEC
Personal Protective Equipment Directive (PPE) - (EU) 2016/425
Radio Equipment Directive (RED) – 2014/53/EU
Explosive Atmosphere Directive (ATEX) - 2014/34/EU

EAC MARKING ERTIFICATION (EURASIAN ECONOMIC UNION)

An EAC mark is essential if consumer products and industrial equipment are sold into Eurasian Economic Union (EAEU). It demonstrates compliance with health and safety legislation and allows the sell into Russia, Belarus, Kazakhstan, Armenia, Kirghistan.

There are two methods to EAC certification depending on product type.

- Certification of Conformity (CoC) which must be issued by an accredited certification body.

- Declaration of Conformity (DoC), which is similar as CE DoC.