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the identification number of the notified body involved in conformity assessment The Measuring Instruments Directive was published on 30 April 2004 in the Official Journal of the EU , but not applied until after 30 October 2006 and there will be a 10-year transition period.
These notified bodies act as Independent Inspection organizations and carry out the procedures as listed in the relevant Modules applied as stated by the relevant directives and regulations. A manufacturer can choose any notified body (notified for the certain directive or regulation and relevant Modules) in any Member State of the European Union.
Additionally, the EU member state accrediting the notified body will then inform the European Commission that the product complies with the essential requirements (or not). [1] [2] [3] More generally, a notified body is an independent, accredited body which is entitled by an authorized accrediting body. Upon definition of standards and ...
The CE marking must appear in a visible, legible and indelible form on the product or, in the case of small components, its packaging. Where relevant, it should be accompanied by the identification number of the Notified body that carried out the conformity assessment procedures. Notified bodies are appointed at the national level by EU Member ...
Define the role and responsibilities of manufacturers, distributors, importers, notified bodies, technical assessment bodies, market surveillance and Member States' authorities as regards the application of this EU regulation. Introduce simplified procedures enabling cost reductions for businesses, especially SMEs.
In Europe the label must show the CE mark and the code number of the certifying/notified body). The CE mark is complemented with the Ex mark: A yellow-filled hexagon with the Greek letters εχ (epsilon chi), followed by the Group, Category, and, if Group II, G or D (gas or dust). Specific types of protection being used will also be marked.
CE number of the certification body (only FFP3) + EN 149: 2009 + the mask class (FFP1, FFP2 or FFP3) + acronym (NR or R) (Note: in case of FFP1 the conformity assessment procedures are done by the manufacturer itself as per Annex IV (Module A) The marking must comply with European Union Directive 89/686 / EEC [8] on PPE.
CE or UKCA; Goods placed on the market in Northern Ireland: CE (if using an EU notified body) CE and UKNI (if using a UK conformity assessment body) [d] Qualifying goods from Northern Ireland placed on the market in Great Britain CE, or CE and UKNI [d] Goods placed on the market in the European Economic Area: CE [e]