Amendment Of The Biocides Act Old Active Ingredient Regulation For The Third Time

Original Language Title: Änderung der BiozidG-Altwirkstoffverordnung zum dritten Mal

Read the untranslated law here: https://www.global-regulation.com/law/austria/2997451/nderung-der-biozidg-altwirkstoffverordnung-zum-dritten-mal.html

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199. Regulation of the Federal Minister for agriculture and forestry, environment and water management, modifies the biocides Act old active ingredient regulation for the third time



On the basis of section 4 paragraph 2 of the biocidal products act - the biocidal products Act, Federal Law Gazette I no. 105/2000, as amended by Federal Law Gazette I no. 151/2004 and the 2009 amendment to the Federal Ministry of law, Federal Law Gazette I no. 3/2009, is prescribed:

The biocidal products act old active ingredient regulation, Federal Law Gazette II No. 353/2008 in the version of regulation BGBl. II No 94/2011, is amended as follows:

1. paragraph 2 paragraph 5:

"(5) If an authorisation for a biocidal product that is subject to the authorisation requirement described in paragraph 1 and 2 and the"



1. a notice referred to in paragraph 1 is reached, or 2.
an application for marketing authorization pursuant to section 11 para 1, 13 or 15 of the biocidal products act has been made, not granted, because the communication referred to in paragraph 1 has not been complemented, or because the request is withdrawn, rejected or dismissed, the admissibility of the placing on the market of the affected biocidal product with the final closure of proceedings or with entry of the legal force of the rejection or refusal of the application ends. When together with a such decision, a the sales period is set within the meaning of article 17, paragraph 6 for the biocidal product concerned biocidal products Act, so the placing of the biocidal product concerned remains authorised yet until the end of that the sales period."

2. paragraph 4 section 5:

"(5) If a registration of a biocidal product with low risk potential, which is subject to the registration obligation described in paragraph 1 and 2 and for the"



1. a notice referred to in paragraph 1 is reached or for the 2nd an application for registration in accordance with article 11 paragraph 2, 14 or 15 of the biocidal products act has been made, does not occur, because the communication referred to in paragraph 1 has not been complemented, or because the request is withdrawn, rejected or dismissed, the admissibility of the placing on the market of the affected biocidal product with low risk potential with the final closure of proceedings or with entry of the legal force of the rejection or refusal of the application ends. When together with a such decision, an off sale period is set within the meaning of § 17 paragraph 6 for the affected low risk biocidal product biocidal products Act, so the placing of the biocidal product with low risk potential remains allowed however until the end of this the sale deadline."

3. in article 8, paragraph 2, the word is 'or' replaced 8 by a comma at the end of the Z; a comma is attached at the end of the Z 9. Following Z 10 to 12 shall be inserted:



"10 the decision of the Commission by July 1, 2011, about the non-inclusion of certain active substances in annex I, IA or IB of to Directive 98/8/EC of the European Parliament and of the Council on the placing on the market of biocidal products (2011/391/EEC), OJ" No. L 175 of the 02.07.2011 p. 28, 11 in the Commission decision of 9 February 2012 concerning the non-inclusion of Flufenoxuron in annex I, IA or IB of to Directive 98/8/EC of the European Parliament and of the Council on the placing on the market of biocidal products for the product-type 18 (2012/77/EEC), OJ No. L 38 of the 11.02.2012 p. 47 or 12 in the Commission decision of 9 February 2012 over the non-inclusion of certain active substances in annex I, IA or IB of to Directive 98/8/EC of the European Parliament and of the Council on the placing on the market of biocidal products (2012/78/EC), OJ No. L 38 of the 11.02.2012 page 48 "4. In section 9 is the word "and" at the end of the Z 36 by a comma replaced; a comma is attached at the end of the Z 37. Following Z 38 to 51 shall be inserted:



"38. the policy 2011/10/EC amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance of Bifenthrin in annex I under the product-type 8, OJ No. L 34 of the 09.02.2011 p. 4, 39. Policy 2011/11/EC amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance (Z, E)-tetradeca-9,12-dienylactetat in annex I under the product type 19, OJ No. L 34 of the 09.02.2011 S. 45, 40 policy 2011/12/EC amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance Fenoxycarb in annex I under the product-type 8, OJ No. L 34 of the 09.02.2011 p. 49, 41st 2011/13/EU directive amending Directive 98/8/EC of the European Parliament and of the Council to nonanoic acid active substance in annex I under the product type 19, OJ No. L 34 of the 09.02.2011 S. 52, 42. 2011/66/EU directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance 4,5 Dichloro 2-octyl-2 H-isothiazol-3-one in annex I under the product-type 8, OJ No. L 175 of the 02.07.2011 p. 10, 43 2011/67/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance abamectin in annex I under the product-type 18, OJ No. L 175 of the 02.07.2011 p. 13, 44. Policy 2011/69/EC amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance imidacloprid in annex I under the product-type 18, OJ No. L 175 of the 02.07.2011 p. 24, 45. 2011/71/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance creosote in annex I under the product-type 8, OJ No. L 195 of the 27.07.2011 p. 46, 46. 2011/78/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance of Bacillus thuringiensis subsp. Israelensis in annex I under the product-type 18, OJ No. L 243 of September p. 7, 47 2011/79/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance fipronil in annex I under the product-type 18, OJ No. L 243 of September p. 10, 48. 2011/80/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance lambda-cyhalothrin in annex I under the product-type 18, OJ No. L 243 of September p. 13 and 49. Policy 2011/81/EC amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance of deltamethrin in annex I under the product-type 18, OJ No. L 243 of September p. 16, 50 2012/2/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council to Kupfer(ii)-OXID, active substances copper(ii) and copper(ii) carbonate in annex I under the product-type 8, OJ No. L 37 of 10.02.2012 S. 60 and 51. 2012/3/EC Directive amending Directive 98/8/EC of the European Parliament and of the Council for the purpose of inclusion of the active substance bendiocarb in annex I under the product-type 18, OJ No. L 37 of 10.02.2012 p. 65 ' 5. The annex is: (see facilities)

Berlakovich