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CE marking is a mandatory legal conformity requirement for certain products sold into the European Union which fall within the scope of CE marking Directives. By affixing the CE marking to a product and by signing the Declaration of Conformity, you are declaring to the EU authorities that the requirements of all applicable Directives have been met. Depending on the Directive, involvement of a ‘Notified Body’ may be required particularly for higher risk products. We can assist you in demonstrating your products’ compliance with the requirements by offering consultancy, training, testing and certification in line with these requirements. To those unfamiliar with the CE marking process, the EU Directives can seem confusing and the simple steps appear complex when addressing requirements in detail. Our advice and technical testing services will speed up the process, getting you to market quickly and will ensure your products are safe, reliable and compliant. We are appointed as a Notified Body against the following CE marking Directives: Low Voltage Directive 2006/95/EC EMC Directive 2004/108/EC Radio and Telecommunications Terminal Equipment Directive 1999/5/EC Machinery Directive 98/37/EC In-vitro Diagnostic Medical Devices Directive 98/79/EEC Active Implantable Medical Devices Directive 90/385/EEC Medical Devices Directive 93/42/EEC CE marking Choose certainty. Add value. TÜV SÜD Product Service Octagon House, Concorde Way, Segensworth North, Fareham, Hampshire, PO15 5RL +44 (0)1489 558100 [email protected] www.tuv-sud.co.uk 2013 © TUV SUD Ltd | UK-MKG-CE-Marking-en-UK CE MARKING IN FIVE STEPS Decide which Directives are applicable to your product Ensure your product is compliant with the applicable Directives by testing and apply the relevant conformity assessment procedures Compile and retail a technical file, which satisfies the require- ments of the Directives Write and sign the Declaration of Conformity and keep the original with the technical file Apply CE marking to the equipment in accordance with the requirements of the Directive Your passport to Europe Your Business Benefits You can sign your Declaration of Conformity with confidence that your products are compliant You receive comprehensive support in following the CE marking procedures Our wide-ranging knowledge of EU directives Our fully accredited and expert testing facilities

CE marking - your passport to Europe

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CE marking is a mandatory legal conformity requirement for certain products sold into the European Union which fall within the scope of CE marking Directives. By affixing the CE marking to a product and by signing the Declaration of Conformity, you are declaring to the EU authorities that the requirements of all applicable Directives have been met. Depending on the Directive, involvement of a ‘Notified Body’ may be required particularly for higher risk products.

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CE marking is a mandatory legal conformity requirement for certain products sold into the European Union whichfall within the scope of CE marking Directives. By affixing the CE marking to a product and by signing the Declaration of Conformity, you are declaring to the EU authorities that the requirements of all applicable Directives have been met. Depending on the Directive, involvement of a ‘Notified Body’ may be required particularly for higher risk products. We can assist you in demonstrating your products’compliance with the requirements by offering consultancy, training, testing and certification in line with these requirements.

To those unfamiliar with the CE marking process, the EUDirectives can seem confusing and the simple stepsappear complex when addressing requirements in detail.Our advice and technical testing services will speed upthe process, getting you to market quickly and willensure your products are safe, reliable and compliant.

We are appointed as a Notified Body against the following CE marking Directives: Low Voltage Directive 2006/95/EC EMC Directive 2004/108/EC Radio and Telecommunications Terminal Equipment

Directive 1999/5/EC Machinery Directive 98/37/EC In-vitro Diagnostic Medical Devices Directive

98/79/EEC Active Implantable Medical Devices Directive

90/385/EEC Medical Devices Directive 93/42/EEC

CE marking

Choose certainty.Add value.

TÜV SÜD Product Service Octagon House, Concorde Way, Segensworth North, Fareham, Hampshire, PO15 5RL +44 (0)1489 558100 [email protected] www.tuv-sud.co.uk

2013

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CE MARKING IN FIVE STEPS

Decide which Directives are applicable to your product

Ensure your product is compliant with the applicable Directives by testing and apply the relevant conformity assessment procedures

Compile and retail a technical file, which satisfies the require-ments of the Directives

Write and sign the Declaration of Conformity and keep the original with the technical file

Apply CE marking to the equipment in accordance with the requirements of the Directive

Your passport to Europe

Your Business Benefits

You can sign your Declaration of Conformity with confidence that your products are compliant

You receive comprehensive support in following the CE marking procedures

Our wide-ranging knowledge of EU directives

Our fully accredited and expert testing facilities