- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (31/01/2020)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance)
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1.An authorisation shall stipulate the terms and conditions relating to the making available on the market and use of the single biocidal product or the biocidal product family and include a summary of the biocidal product characteristics.
2.Without prejudice to Articles 66 and 67, the summary of the biocidal product characteristics for a single biocidal product or, in the case of a biocidal product family, the biocidal products within that biocidal product family, shall include the following information:
(a)trade name of the biocidal product;
(b)name and address of the authorisation holder;
(c)date of the authorisation and its date of expiry;
(d)authorisation number of the biocidal product, together with, in the case of a biocidal product family, the suffixes to apply to individual biocidal products within the biocidal product family;
(e)qualitative and quantitative composition in terms of the active substances and non-active substances, knowledge of which is essential for proper use of biocidal products; and in the case of a biocidal product family, the quantitative composition shall indicate a minimum and maximum percentage for each active and non-active substance, where the minimum percentage indicated for certain substances may be 0 %;
(f)manufacturers of the biocidal product (names and addresses including location of manufacturing sites);
(g)manufacturers of the active substances (names and addresses including location of manufacturing sites);
(h)type of formulation of the biocidal product;
(i)hazard and precautionary statements;
(j)product-type and, where relevant, an exact description of the authorised use;
(k)target harmful organisms;
(l)application doses and instructions for use;
(m)categories of users;
(n)particulars of likely direct or indirect adverse effects and first aid instructions and emergency measures to protect the environment;
(o)instructions for safe disposal of the product and its packaging;
(p)conditions of storage and shelf-life of the biocidal product under normal conditions of storage;
(q)where relevant, other information about the biocidal product.
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