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03 03(nFtCDCQo cu n c Eu '0F1ieP,r1rt 0 LD 'DP CD(u CLIDaR1 m0F arntCLiv1CI6: a25R0 rtP0 3R(up 1 'did 1 0Ldb9R8 4(u CL(DCcn0m 'due. RTL? 0(Dr t!CLP.(u(DMC'd raid 0P rt1rt10 'DP a 0ID(Dirt! Fsr0 DR0,r.
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What is c e?
CE stands for Conformité Européene, which translates to European Conformity. It is a mandatory conformity marking for certain products sold within the European Economic Area.
Who is required to file c e?
Manufacturers or authorized representatives of products that fall under the scope of CE marking are required to file CE.
How to fill out c e?
Filling out CE involves conducting the necessary conformity assessments, ensuring compliance with relevant European Union directives, creating a technical file, and affixing the CE marking to the product.
What is the purpose of c e?
The purpose of CE is to indicate that a product conforms to the essential requirements of relevant EU directives, ensuring its safety, health, and environmental compliance before it is placed on the market.
What information must be reported on c e?
CE marking does not require specific reporting. However, the product's technical documentation must be available, including information about the conformity assessment procedure, test reports, and other relevant data.
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