Import / Export Location World Wide
To export product to European Union countries you require CE mark certified product. To get CE mark from European Union Approved Notified Bodies, we can help you to get certified your products to easily export to European Union Countries. CE mark products certification work like passport to European Union Market.
CE Marking
Export To Portugal
DCS provides services of CE certification according to the following EU Directives:
* Construction products directive (CPD) 89/106/EEC
* Electrical equipment designed for use within certain operating voltages directive 73/23 EEC
* ATEX Directive 94/9/ EC (for the products for use in potentially explosive atmospheres)
* Pressure equipment directive 97/23/EC (PED)
* The medical device directive 93/42/EEC (2007/47/EC)
* The active implantable medical device directive 90/385/EEC
* The In-Vitro Diagnostic Directive 98/79/EC, * Personal protective equipment directive 89/686/EEC
* The measuring instruments Directive 2004/22/EC (MID)* The toy safety Directive 88/378/EEC
* electromagnetic compatibility Directive 2004/108/EC (EMC)
* machinery Directive 2006/42/EC (MD), * low-voltage Directive 2006/95/EC (LVD)
* The radio communications and telecommunications terminal equipment Directive 1999/5/EC (R&TTE)
* The non-automated weighing nstruments Directive 90/384/EEC (NAWI) (93/68/EEC)
* The Directive on efficiency requirements for new hot-water boilers (water heaters), working on liquid or gaseous fuel92/42/EEC, The Directive on the elevators and hoisting mechanism 95/16/EC
*The simple pressure vessels directive 2009/105/EC (SPVD), The gas appliances directive 2009/142/EC
The stages of further work, expected results and timeframe for completion of the European certification on the European certificate of conformity.
STAGE 1 – «CONSULTING» (realization terms: 20-25 working days)
Consulting services on the EU Directives, necessary for the assessment of conformity of products to the requirements of the European Union, a translation of the necessary documentation (Specifications, instructions for use), as well as the determination of the value of the certification by europeon notified body.
The expected outcome is a report, which reflects the EU Directive, the certification scheme, the list of harmonized standards and other documents, on the basis of which products must be evaluated to the requirements of the European Union.
STAGE 2 – «TESTING» (realization terms: 15-20 working days)
Carrying out tests in the laboratory. This stage involves testing of samples of production declared on certification in the Laboratory (it is possible to provide on the territory of India in the presence of experts of Notified Bodies, or in the laboratory in EU).The expected Result is the receipt of testing protocol.
STAGE 3 – «PREPARATION OF DOCUMENTATION FOR THE AUDIT OF THE ENTERPRISE» (realization terms: 5 – 7 working days)Involves the collection and filing of the necessary documentation, the list of which is provided to the customer on the first stage and the preparation of the plan of the certification audit.
STEP 4 – «AUDIT IN THE WORKPLACE» (realization terms: 10 – 14 working days)
Audit in the workplace. Experts of Notified Bodies and two representatives of the DCS visit the enterprise.
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