CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985. CE marking on a product is the manufacturer’s declaration that the product complies with the essential requirements of all the Directives that apply to it. It indicates to the appropriate bodies that the product may be legally offered for sale in their country. The requirements for CE marking differ across all the Directives and may also vary for different products within a Directive. Depending on the criticality of product, CE marking may be as simple as formulating aonly technical file, or as complex as having to submit your products on regular basis to independent scrutiny. Third party testing, systems assessment, and technical file assessments may be mandatory, but sometimes the manufacturer’s unverified claim is all that’s asked for.
CE originated as an abbreviation of ConformitéEuropéenne, meaning European Conformity, but is not defined as such in the relevant legislation. The CE marking is a symbol of free marketability in the European Economic Area
How can USL International help you with CE marking?
USL International will help you gain easier access to the European market by ensuring your product meets all the CE mark requirements. If you manufacture or import products which fall within the scope of one or more of the New Approach Directives you will then need professional guidance on how to meet all the essential requirements of these directives. USL International has the capabilities and expertise for professional guidance –
Identification of Directive
Identification of applicable Harmonized standard
Testing and evaluation of your products
Evaluation and preparation of Technical File
GAP analysis and pre-certification audit
Certification audit
USL International Deals In Following Directives
| Low Voltage Directives (LVD) 2006/95/EC | (View Details) |
| Machine Directive – 2006/42/EC | (View Details) |
| Construction Products Regulations (CPR) 305/2011 | (View Details) |
| Personal Protective Equipment (PPE) 89/686/EEC | (View Details) |
| Medical Devices (MDD) 93/42/EEC | (View Details) |
| Lifts 95/16/EC | (View Details) |
| Electromagnetic compatibility (EMC) 2004/108/EC | (View Details) |
| Pressure Equipment Directive (PED) 97/23/EC | (View Details) |
| Simple Pressure Vessels 2009/105/EC | (View Details) |
| In Vitro Diagnostics Directive (IVDD) 98/79/EC | (View Details) |
| Safety of toy- 2009/48/EC | (View Details) |
| Gas Appliance Directive 2009/142/EC | (View Details) |
| ATEX Directive – 2014/34/EU | (View Details) |
| R&TTE Directive – 1999/5/EC | (View Details) |
What’s involved in product certification?
Gap analysis : If you need our help at the outset, we can advise on any areas that may need attention.
Pre-Assessment : If you wish to be reassured that you are ready for full assessment
Technical support during the certification process by some of the best trained and most competent staff available.
Dedicated team always available by email or telephone.
Technical advice; on interpretation and requirements of standards and Directives
Timescale and project management
Product certification
Why Choose USL International for Product Certification
Experience- have a good and big team of expertise and experience in helping its customers through these often complex processes.
Accessible & ready-our dedicated team is ready and waiting to help you comply with your chosen product certification needs
Speed to marke tour specialist expertise means that USL can deliver one of the fastest speed-to-market services available giving you the advantage and head start over your competitors.
Accreditation & collaborations
USL International has the collaborations and Dealing with different EU notify body for different Directives as per customer needs.