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GUIDE NAWI - Cyprus Organization for the Promotion of Quality

GUIDE NAWI - Cyprus Organization for the Promotion of Quality

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Guide on <strong>NAWI</strong> DirectiveEuropeAid /114385/D/SV/CYInstruments shall bear no characteristics that can cause, directly or indirectly, indications whoseinterpretation is not easy or straight <strong>for</strong>ward.Instruments shall safeguard customers against incorrect sales transactions due to <strong>the</strong>irmalfunctioning.Auxiliary indicating devices and extended indicating devices are not permitted.Supplementary devices are permitted only if <strong>the</strong>y cannot lead to fraudulent use.Instruments similar to those normally used <strong>for</strong> direct sales to <strong>the</strong> public which do not satisfy <strong>the</strong>requirements <strong>of</strong> this section must carry near to <strong>the</strong> display <strong>the</strong> indelible marking ‘Not to be used<strong>for</strong> direct sales to <strong>the</strong> public’.15. PRICE LABELLING INSTRUMENTSPrice labeling instruments shall meet <strong>the</strong> requirements <strong>of</strong> price indicating instruments <strong>for</strong> directsales to <strong>the</strong> public, as far as applicable to <strong>the</strong> instrument in question. The printing <strong>of</strong> a price labelshall be impossible below a minimum capacity.EC TYPE-EXAMINATIONApplications <strong>for</strong> EC type-examination are to be made by <strong>the</strong> manufacturer or by his authorisedrepresentative established within <strong>the</strong> Community to a single notified body.They are to include:• <strong>the</strong> name and address <strong>of</strong> <strong>the</strong> manufacturer; and, if <strong>the</strong> application is being lodged by <strong>the</strong>authorised representative, also his name and address,• a written declaration that an application has not been lodged with any o<strong>the</strong>r notified body,• <strong>the</strong> design documentation described in Annex III <strong>of</strong> <strong>the</strong> Directive.The applicant must place at <strong>the</strong> disposal <strong>of</strong> <strong>the</strong> notified body a prototype instrument, representative <strong>of</strong> <strong>the</strong>production envisaged.The notified body is to• examine <strong>the</strong> design documentation and verify that <strong>the</strong> prototype has been manufactured inaccordance with that documentation,• agree with <strong>the</strong> applicant where <strong>the</strong> examinations and/or tests are to be carried out;• where <strong>the</strong> manufacturer has not used <strong>the</strong> relevant specified standards, per<strong>for</strong>m, or haveper<strong>for</strong>med, <strong>the</strong> appropriate examinations and/or tests to check whe<strong>the</strong>r <strong>the</strong> solutions adopted by<strong>the</strong> manufacturer meet <strong>the</strong> essential requirements; and,• where <strong>the</strong> manufacturer has used <strong>the</strong> relevant specified standards, per<strong>for</strong>m, or have per<strong>for</strong>med,<strong>the</strong> appropriate examinations and/or tests to check whe<strong>the</strong>r those standards have been appliedeffectively, <strong>the</strong>reby assuring con<strong>for</strong>mity with <strong>the</strong> essential requirements.

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