CE Marking In Chennai
Eurotech Providing CE Marking Certification Service In Chennai City .
The CE Marking / formerly EC mark, is a mandatory conformity mark for certain products sold within the European Economic Area (EEA) since 1985. The CE mark certification is also found on products sold outside the EEA that are manufactured in / designed to be sold in the EEA for more information
The CE Marking certification, which is for a product or its packaging is considered proof that a product has met the requirements of the harmonized Europe standard. The Europe Commission, which administers the program, describes the CE Marking certification as a passport for goods to be sold freely within the internal Europe Market. It is required by law if the product falls under one of the New Access Directives. It is not a quality Marking nor is it a marking for consumers. Intended for Member State authorities, it is the visible icon to those authorities that your product is in compliance with the New Approach Directives. All manufacturers are required to paste the CE marking to products that are governed by New Approach Directives. CE mark on a product indicates to all authorities that the product is in compliance with the essential health & safety requirements of all directives that apply to the product.
Eurotech providing CE Marking Certification in 6 Steps :
- Identify the applicable directive(s)
- Identify the applicable requirements of the directive(s)
- Identify an appropriate route to conformity
- Assessment of the product’s conformity
- Compile the technical documentation
- Make a declaration and affix the CE Marking
Benefits of CE Mark
The CE Mark is a kind of trade passport for the European marketplace: it allows the manufacturer to freely circulate their product throughout the Eighteen countries of the European Economic Area EEA.
There is only one set of requirements & procedures to comply with in designing & manufacturing a product for the entire EEA. Various conflicting national regulations are eliminated. As a result, the product no longer needs to be adapted to the specific requirements of the different member states of the EEA. In addition, it may be considered a benefit that by implementing the requirements, the product will be safer for the user & this may also reduce damage & liability claims
CE Mark is a conformity marking consisting of the letters CE & taking the form as shown here. CE certification is an abbreviation, French for 'European Conformity'. The CE mark symbolizes that a product it is affixed to is in conformity with all relevant essential requirements of the European technical regulations Directives, & that the product compliance has been established using the appropriate conformity assessment procedures. The 'essential requirements' are requirements related to product safety, public health & consumer protection.
CE Mark is obligatory for any product covered by one / more of the European technical regulations requiring the affixing of the CE marking. Without the CE Mark, these products are not allowed to be placed or to be put into service in Europe. In this regard, the CE Mark sometimes is called a 'trade passport', because like carrying a passport when entering a country, the CE Mark is required for market access.
Eurotech European CE Mark certification procedure has been mainly set up to:
1.Identify the Directives that are applicable to your product. You can download these directives free of charge from the European Union website
2.Identify the conformity assessment procedure that must be taken. This could be self declaration, involve testing, inspection or quality system assessment from a Notified Body or a combination of these. The conformity assessment procedure will differ depending on your product and the Directive in respect of which you will be CE mark.
3.Determine the dates by which you must take action. This will be the date that the Directive comes into force. The majority of directives are already in force. In these cases, it is an offence to place a product on the market without CE mark because it indicates a presumption of conformity with all relevant Legislation
4.Identify if there are any Harmonised European Standards applicable to your product. These are not always mandatory for manufacturers although there is a presumption that conformity to these standards will give conformity with the relevant part of the Directive. Whenever possible or appropriate, manufacturers should follow harmonised standards.
5. Ensure the product complies with all the essential requirements of the Directives. Take appropriate measures to comply or identify existing data & test reports.
6.Identify whether independent assessment of your conformity to the Directive, or some aspects of it, is required from a Notified Body. This will be stated in the directive and is dependent upon the product you are CE mark. You must not affix CE mark to your product until all necessary certifications have been obtained from the Notified Body.
7.Maintain Technical Documentation required by the Directives. Your technical documentation should support your compliance with the requirements of the Directive. It is essential to retain this documentation.
8.Prepare the Declaration of Conformity & the required supporting evidence. The Declaration of Conformity along with the Technical Documentation should be available to Competent Authorities EU Members upon request.
9. Check that no other purely national requirements exist in the countries where the product will be sold. These may include national standards, labeling or packaging requirements.
10.Affix CE mark on your product /or its packaging & accompanying literature as stated in the directive.
With the help of the European conformity assessment procedures, the authorities can ascertain that the products that are placed on the market comply with the requirements as stated in the regulations of the directives. The CE mark is consequently largely for the benefit of the authorities. However, safe products are also necessary for the end user in the work or consumer environment.
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CE Mark Certification Code of Directives and Titles provided by Eurotech:
Title of Directive | No. / Code of Directive | |
1 | Low voltage | 73/23/EEC |
2 | Simple pressure vessels | 87/404/EEC |
3 | Safety of toys | 88/378/EEC |
4 | Electromagnetic compatibility | 89/336/EEC |
5 | Personal protective equipment | 89/686/EEC |
6 | Non-automatic weighing instruments | 90/384/EEC |
7 | Active implantable medical devices | 90/385/EEC |
8 | Appliances burning gaseous fuels | 90/396/EEC |
9 | Explosives for civil uses | 93/15/EEC |
10 | Medical devices | 93/42/EEC |
11 | Equipment and protective systems intended for use in potentially explosive atmospheres | 94/9/EC |
12 | Recreational craft | 94/25/EC |
13 | Lifts | 95/16/EC |
14 | Interoperability of the Trans-European high-speed rail system | 96/48/EC |
15 | Pressure equipment | 97/23/EC |
16 | Machinery | 98/37/EC |
17 | In vitro diagnostic medical devices | 98/79/EC |
18 | Radio and telecommunications terminal equipment | 99/5/EC |
19 | Construction Products | 89/106/EEC |
20 | Hot Water Boilers fired with liquid or gaseous Fuels | 88/378/EEC |
21 | Cableway Installations | 2000/9/EC |
Kindly send us your testing requirements with the product technical details to submit you our testing charges.
We are waiting for your earliest reply.
You can call or write us for any clarification.
Thanks & Regards,For, Eurotech ACS Pvt. Ltd.
Puneet Sharma
M: +91.8196980555
ce.marking.certification@gmail.com
Offices : - INDIA,OMAN, UK, US, CANADA, IRELAND.
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