It's a tool to build:
- economic growth
- trade, free movement of goods
- transparency
- public policies
On the european territory, the "new approach" directives were agreed in 1985, and the harmonized standards now give presumption of conformity to general requirements of the directive.
There are 2 european directives for PPEs:
- Directive for end users : 89/656 (use of PPEs marked CE)
- Directive for manufacturers : 89/686 (conception and placing on the market of products marked CE)
Article 8 of the directive defines 3 categories of PPEs. Those categories define the documentation which must be linked to the product, and the level of tests to be reached.
- categoryI : minor risks (superficial lesions)
- category II : intermediate risks
- category III : mortal risks or irreversible lesions
Those tests are done by Notified Bodies than can be chosen in a european list of certified laboratories. According to the results of the tests, the NB can deliver a CE Type Examination, can validate the user's manual and the technical file of the product. It will then have a specific marking and will be sold with its user's manual. The end user can also ask for the technical data sheet and the Certificate of Conformity.
For products category III an annual quality control of the production will also be done by a NB (CE marking + 4 numbers).
Marking examples :
Do you want to test your knowledge ?<iframe src="https://spreadsheets1.google.com/embeddedform?formkey=dHh6VUNoTENFVktBd1lFWUVfbEswbWc6MQ" width="760" height="1222" frameborder="0" marginheight="0" marginwidth="0">Chargement en cours...</iframe>
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