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Shenzhen Bory Technology Service Co.,Ltd.

Products >> How to achieve CE mark approval, CE testing and meet all CE mark

How to achieve CE mark approval, CE testing and meet all CE mark

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Product Name: How to achieve CE mark approval, CE testing and meet all CE mark
Supply Ability: 2014
Related proudcts ce testing,
Specifications How to achieve CE mark approval, CE testing and meet all CE mark
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here are a series of steps outlined below for CE mark approval. Depending upon your product and the nature of the risks it presents:
***ermine if any directives apply to your product. If more than one applies you will have to comply with all of them.

***ermine the extent to which your product complies with the essential requirements for design and manufacturing in the applicable directive(s).

Choose the conformity assessment procedure from the options (modules) called out by the directive for your product. There are several modules available for the Conformity Assessment Procedures as listed below:

Module A: internal production control
Module Aa: intervention of a Notified Body
Module B: EC type-examination
Module C: conformity to type
Module D: production quality assurance
Module E: product quality assurance
Module F: product verification
Module G: unit verification
Module H: full quality assurance

The directives often use a series of questions about the nature of your product to classify the level of risk and refer to a chart called "Conformity Assessment Procedures". The chart includes all of the acceptable options available to a manufacturer to certify their product and affix the CE Marking.
Minimal RiskOptions for products with minimal risk include self certification where the manufacturer prepares a Declaration of Conformity and affixes the CE Marking to their own product.
Greater RisksMany directives require products/systems with greater risks to be independently certified; this must be done by a "Notified Body". This is an organization that has been nominated by a Member Government and has been notified by the European Commission. Notified bodies serve asindependent test labs and perform the steps called out by directives. They must have the necessary qualifications to meet the testing requirements set forth in the directives. Notified bodies may be a private sector organization or a government agency. Manufacturers may choose a notified body in any member state of the European

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