Eucert ICSPL is a leading certification body in the field of product certification and CE Marking certification is a core area of Eucert. We are having a great experience in the field of CE Marking. We deliver our best possible efforts to complete all the requirements of CE compliance as per European Harmonized EN/IEC Standards. We are working in following scope of CE Marking Certifications (As per European Directives and standards):
- Machinery Directive (2006/42/EC) – MD
- Pressure Equipment Directive (97/23/EC) – PED
- Construction Products Regulation (EU) No. 305/2011 – CPR
- Low Voltage Directive (Electrical Equipment) (2006/95/EC) – LVD
- EMC Directive (2004/108/EC) – EMC
- General Product Safety Directives(2001/95/EC) – GPSD
- Medical Device Directive (93/42/EEC) – MDD
- In-vitro Diagnostic Medical Device Directive (98/79/EC) – IVD
Often CE marking described as a trade passport to enables the free movement of products within the European market.
The CE marking is a key indicator of a product’s compliance with European Union health, safety and regulations and environmental protection directives.
If your product comes under the scope of a directive requiring CE marking you must ensure that the product complies with the applicable requirements of harmonized standards and affix the CE mark before placing it in the market in the European Economic Area.
Second hand or old used products from outside the EEA that are placed in the EEA market for the first time, also require CE marking.
You cannot affix the CE mark logo to the products which are not covered by the relevant European directives;
By affixing the CE marking, you are responsible for your product’s compliance with the requirements of the relevant directives and harmonized standards.
The CE mark is a marking that consist of the initials ‘CE’ in the following form:
The CE marking is not required for items like :
- chemicals
- cosmetics
- foodstuffs
- pharmaceuticals