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PESTICIDES CONTROL ACT (CAP. 430)Biocides (Amendment) Regulations, 2009
IN exercise of the powers conferred by articles 4 and 5 of the Pesticides Control Act, the Minister for Resources and Rural Affairs, in consultation with the Prime Minister and with the Minister for Social Policy, has made the following regulations:-
Title and scope. L.N. 294 of 2004
.
1. (1) The title of these regulations is the Biocides (Amendment) Regulations, 2009 and they shall be read and construed as one with Biocides Regulations, 2004, hereinafter referred to as “the principal regulations”.(2) The scope of these regulations is to transpose Commission Directive 2007/47/EC of the European Parliament and of the Council
of 5 September 2007 amending Council Directive 90/385/ EEC on the approximation of the laws of the Member States relating to active
implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing
of biocidal products on the market, Commission Directive
2008/15/EC of 15 February 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include clothianidin as
an active substance in Annex IA thereto, Commission Directive
2008/16/EC of 15 February 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include etofenprox as an
active substance in Annex I thereto, Commission Directive
2008/75/EC of 24 July 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include carbon dioxide as an
active substance in Annex I thereto, Commission Directive
2008/77/EC of 25 July 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include thiamethoxam as an
active substance in Annex I thereto, Commission Directive
2008/78/EC of 25 July 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include propiconazole as an
active substance in Annex I thereto, Commission Directive
2008/79/EC of 28 July 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include IPBC as an active substance
in Annex I thereto, Commission Directive 2008/80/ EC of 28 July 2008 amending Directive 98/8/EC of the European Parliament and of
the Council to include cyclohexylhydroxydiazene
1-oxide, potassium salt (K-HDO), Commission Directive 2008/81/
EC of 29 July 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include difenacoum as an active substance in Annex I thereto, Commission Directive 2008/85/EC of 5 September 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include thiabendazole as an active substance in Annex I thereto, and Commission Directive 2008/86/EC of 5 September 2008 amending Directive 98/8/EC of the European Parliament and of the Council to include tebuconazole as an active substance in Annex I thereto.
2. (1) In regulation 2(2) of the principal regulations, immediately after item (r) thereof, there shall be added the following:-“(s) provisions concerning in vitro diagnostic medical devices.”
3. In Schedule III to the principal regulations, immediately after item 3 thereof, there shall be added the following new items:-B 45
Amends regulation
2 of the principal regulations.
Amends Schedule III to the principal regulations.
B 46 VERŻJONI ELETTRONIKA
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Ippubblikat mid-Dipartiment tal-Informazzjoni (doi.gov.mt) — Valletta — Published by the Department of Information (doi.gov.mt) — Valletta
Mitbugħ fl-Istamperija tal-Gvern fuq karta riċiklata — Printed at the Government Printing Press on recycled paper <.. image removed ..>
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URL: http://www.worldlii.org/mt/legis/laws/pca430br200916o2009538