5. The information referred to in the second subparagraph of paragraph 4 shall include all available details, in particular the data necessary for the identification of the non-compliant product, the origin of the product, the nature of the non-compliance alleged and the accessibility requirements with which the product does not comply, the nature and duration of the national measures taken and the arguments put forward by the relevant economic operator. In particular, the market surveillance authorities shall indicate whether the non-compliance is due to either:
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(a)
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the failure of the product to meet the applicable accessibility requirements; or
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(b)
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the shortcomings in the harmonised standards or in the technical specifications referred to in Article 15 conferring a presumption of conformity.
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