Division A Any undertaking intending to manufacture or import into a Member State consumer products for which the intended use is likely to lead to a new class or type of practice, shall provide the competent authority of this Member State with all relevant information, as to the:

intended use of the product;

technical characteristics of the product;

in the case of products containing radioactive substances, information as to their means of fixation;

dose rates at relevant distances for the use of the product, including dose rates at a distance of 0,1 m from any accessible surface;

expected doses to regular users of the product.