Difference between revisions of "CE"
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The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. | The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. | ||
The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure. | The mark consists of the CE logo and, if applicable, the four digit identification number of the [[Notified Body]] involved in the conformity assessment procedure. | ||
Author: [[User:Laschober Gerhard|Laschober Gerhard]] 05:37, 12 February 2016 (CET) | Author: [[User:Laschober Gerhard|Laschober Gerhard]] 05:37, 12 February 2016 (CET) | ||
Revision as of 07:53, 12 February 2016
- high-resolution terminology - matching measurements at high-resolution
CE
Description
CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA).
Reference: http://ec.europa.eu/growth/single-market/ce-marking/
MitoPedia concepts: "MitoFit Quality Control System" is not in the list (MiP concept, Respiratory state, Respiratory control ratio, SUIT concept, SUIT protocol, SUIT A, SUIT B, SUIT C, SUIT state, Recommended, ...) of allowed values for the "MitoPedia concept" property.
MitoFit Quality Control System"MitoFit Quality Control System" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property.
The CE marking is also found on products sold outside the EEA (EU plus Iceland, Norway, Liechtenstein, Switzerland, Turkey) that are manufactured in, or designed to be sold in, the EEA.
"CE" originated as an abbreviation of Conformité Européenne, meaning European Conformity, but is not defined as such in the relevant legislation.
The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.
The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure.
Author: Laschober Gerhard 05:37, 12 February 2016 (CET)
