Amendment Of The Act Concerning The Conditions Of Placing Of Biocidal Products On The Market

Original Language Title: změna zákona o podmínkách uvádění biocidních přípravků na trh

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136/2010 Sb.



LAW



of 21 June 1999. April 2010,



amending Act No 120/2002 Coll., on conditions for the placing of biocidal

products and active substances on the market and amending some related

laws, as amended



Parliament has passed the following Act of the United States:



Article. (I)



Act No 120/2002 Coll., on conditions for the placing of biocidal products and

active substances on the market and amending certain related laws, in

amended by Act No. 186/2004 Coll., Act No. 127/2005 Coll. and Act No.

297/2008 Coll., is amended as follows:



1. Footnote 1 is added:



"1) European Parliament and Council Directive 98/8/EC of 16 December 2002. February 1998

concerning the placing of biocidal products on the market.



Commission Directive 2006/140/EC of 20 May 1999. in December 2006, amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance sulfurylfluorid in annex I to that directive.



Commission Directive 2006/50/EC of 29 April 2004. May 2006 amending

Annex IVA and IVB European Parliament and Council Directive 98/8/EC on the

placing of biocidal products on the market.



Commission Directive 2007/20/EC of 3 June 2003. April 2007 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance dichlofluanid in annex I to that directive.



Commission Directive 2007/69/EC of 29 April 2004. November 2007 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance difethialone in annex I to that directive.



Commission Directive 2007/70/EC of 29 April 2004. November 2007 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance carbon dioxide in annex IA to the directive.



Commission Directive 2008/75/EC of 24 July 2003. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance carbon dioxide in annex I to that directive.



Commission Directive 2008/77/EC of 25 March 2002. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance thiamethoxam in annex I to that directive.



Commission Directive 2008/78/EC of 25 March 2002. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance in annex I to that Propiconazole directive.



Commission Directive 2008/79/EC of 28 June 1999. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance to the IPBC annex I to that directive.



Commission Directive 2008/80/EC of 28 June 1999. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance cyklohexyl (hydroxy) diazen-1-oxide, potassium salt (K-HDO) into

Annex I to that directive.



Commission Directive 2008/81/EC of 29 April 2004. July 2008 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance difenakum in annex I to that directive.



Commission Directive 2008/85/EC of 5 July 2004. September 2008 amending Directive

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active substance

thiabendazole in annex I to that directive.



Commission Directive 2008/86/EC of 5 July 2004. September 2008 amending Directive

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active substance

tebukonazol in annex I to that directive.



Commission directive 2009/84/EC of 28 June 1999. July 2009 amending

Annex I to the directive of the European Parliament and Council Directive 98/8/EC in order to

sulfurylfluorid as active substance in annex I to that directive.



Commission directive 2009/85/EC of 29 April 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance kumatetralyl in annex I to that directive.



Commission directive 2009/86/EC of 29 April 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance in annex I to that fenpropimorph directive.



Commission directive 2009/87/EC of 29 April 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

indoxacarb in annex I to that directive.



Commission directive 2009/88/EC of 30 March 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substances thiacloprid in annex I to that directive.



Commission directive 2009/89/EC of 30 March 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance nitrogen in annex I to that directive.



Commission directive 2009/91/EC of 31 October. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance tetraboritan disodium in annex I to that directive.



Commission directive 2009/92/EC of 31 October. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance bromadiolon in annex I to that directive.



Commission directive 2009/93/EC of 31 October. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance and-chloralose, in annex I to that directive.



Commission directive 2009/94/EC of 31 March 2004. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

boric acid substances in annex I to that directive.



Commission directive 2009/95/EC of 31 October. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

Aluminium phosphide releasing fosfin substances in annex I to that directive.



Commission directive 2009/96/EC of 31 October. July 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

disodium oktaboritan tetrahydrate substances in annex I to that directive.



Commission directive 2009/98/EC of 4 April 2003. August 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

substance boron trioxide in annex I to that directive.



Commission directive 2009/99/EC of 4 April 2003. August 2009 amending

European Parliament and Council Directive 98/8/EC for the purpose of inclusion of the active

the substance chlorofacinon in annex I to that directive.



European Parliament and Council directive 2009/107/EC of 16 December 2002. September 2009,

amending Directive 98/8/EC concerning the placing of biocidal products on the market,

as regards the extension of certain time limits ".



2. In article 16(1). 2 (a). (b)) item 1:



"1. to 14. may 2014, with the exception of data protected under specific

laws on inventions, rationalization proposals and industrial

patterns and their protection ^ 10), which will continue the protection of the

information to the time specified by the special legislation,

up to 14. may 2014, ".



3. in article 16 paragraph 1. 2 (a). d) point 1 shall read:



"1. to 14. may 2014, with the exception of data protected under specific

laws on inventions, rationalization proposals and industrial

patterns and their protection ^ 10), which will continue the protection of the

information to the time specified by the special legislation,

up to 14. may 2014, ".



4. In section 35 para. 3 (b). and that is the word ")" shall be replaced by the word "which" and

the words "14. May 2010 "shall be replaced by the words" 14. may 2014 ".



5. In annex 2, the following item No. 1, 6 to 15, 17 to 25, 27 and 28,

shall be added:

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

(I) the number and the generic name and IUPAC name and MinimálníI released and the time limit for compliance with (I) the date of (I) the product-type and the specific conditions and

I I I the identification numbers and I and all of the requirements as well as the validity of the I I I

I I I I I I effective (with the exception of (I) the inclusion of I I I

I I I I I I the substance in products I I I I

I I I I I in biocidal products containing more than I I I I

I I I I přípravkuI even than the one active I I I I

I I I I I I substance, for which I I I I

I I I I I I will be putting the deadline I I I I

I I I I I I on the market set out in I I I I

I I I I I I I I I I last

I I I I I I I I I decision and the

I I I I I I the inclusion, if I I I I

I I I I I I of I I I I

I I I I I I s) I I I I

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I 1 I sulfurylfluorid I sulfurylfluorid I 994 g/kg and 1. 30 July 2011. 30 June 2013. June 2021 and 18 I 1) products may also sell

I I I EC No: 220-281-5 I I I I I I only trained professionals and even

I I I the CAS number: 2699-79-8 I I I I I I používányrovněž I may be


I I I I I I I I I only trained experts. (I)

I I I I I I I I I 2) it is necessary to take appropriate and

I I I I I I I I I measures to protect people and

I I I I I I I I I carrying out fumigation and I

I I I I I I I I I the ventilation of buildings and

I I I I I I I I I and other enclosed areas. (I)

I I I I I I I I I 3) labels and/or

I I I I I I I I I product and safety data sheets

I I I I I I I I I States that všechnypotraviny and

I I I I I I I I I I must be removed from the

I I I I I I I I I the room before her and

I I I I I I I I I furmigací. (I)

I I I I I I I I I 4) the permit holder must also

I I I I I I I I I monitor the concentration and

I I I I I I I I I sulfurylfluoridu in the remote and

I I I I I I I I I the troposphere, and every fifth year, and

I I I I I I I I I starting with the last five I

I I I I I I I I I years ago after vystaveníoprávnění and

I I I I I I I I I držiteléoprávnění I served

I I I I I I I I I to be placed on the market directly and

I I I I I I I I I the Commission reports on the control. (I)

I I I I I I I I I the limit of detection for the analysis is the

I I I I I I I I I at least 0.5 ppt (equivalent to (I)

I I I I I I I I I sulfurylfluoridu 2.1 ng/m3 and

I I I I I I I I I in the remote troposphere). (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I 6 I tebukonazol I l-(4-chlorophenyl)-I 950 g/kg and 1. April 2010 I 31. March 2012 and 31. March 2020 and 8, even when using the product and

I I I 4.4-dimethyl-I I I I I I legal or business and

I I I 3-[(lH-l, 2,4-triazole-1-I I I I I I or the nonentrepreneurial natural and

I I I yl) methyl] pentan-3-ol I I I I I I a person, because I krizikům

I I I EC No: 403-640-2 I I I I I I for the soil and the aquatic compartment, and

I I I CAS No: 107534-96-3 I I I I I I take appropriate measures to mitigate and

I I I I I I I I I the risks in order to protect and

I I I I I I I I I the environment. The Holder And The

I I I I I I I I I the authorisation and shall in particular indicate

I I I I I I I I I on the label and/or even

I I I I I I I I I I a safety data sheet

I I I I I I I I I of the biocidal product and

I I I I I I I I I allowed for industrial and

I I I I I I I I I use freshly treated and

I I I I I I I I I the wood must be poošetření and

I I I I I I I I I stored under the protective and

I I I I I I I I I cover or on impermeable and

I I I I I I I I I hard bedrock, so that

I I I I I I I I I avoid direct spills and

I I I I I I I I I soil or water, and that is also

I I I I I I I I I leaking biocidal product and

I I I I I I I I I I must shromažďovatpro

I I I I I I I I I reuse or even

I I I I I I I I I for destruction. (I)

I I I I I I I I I the Ministry of health and

I I I I I I I I I will not allow for even

I I I I I I I I I in situ in the treatment of wood and

I I I I I I I I I outdoor environment or for

I I I I I I I I I I budevystaveno wood

I I I I I I I I I a permanent působenívody, even

I I I I I I I I I unless I předloženéúdaje

I I I I I I I I I demonstrate that I

I I I I I I I I I the basis of the evaluation under paragraph 6 (I)

I I I I I I I I I will fulfill the requirements of section 7 (2). 1 I

I I I I I I I I I to 4 with the use of reasonable and

I I I I I I I I I measures to mitigate the risks, and

I I I I I I I I I will if necessary. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And 7 and carbon dioxide and carbon dioxide and 990 ml/l and 1. November 2009 and 31. October 2011 and 31. October 2019 and 14 as well as the Ministry of health, and

I I I EC No: 204-696-9 I I I I I I I the Ministry of

I I I CAS No: 124-38-9 I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for authorisation and

I I I I I I I I I a particular product in the I

I I I I I I I I I accordance with the § 6 and 7hodnotí and

I I I I I I I I I population that can be

I I I I I I I I I exposed his work and I

I I I I I I I I I use, or even

I I I I I I I I I exposure that were not even

I I I I I I I I I presentable represented

I I I I I I I I I I risk assessment

I I I I I I I I I the level of European and

I I I I I I I I I the community, if it is even

I I I I I I I I I needed. At the annual and

I I I I I I I I I I the authorisation of

I I I I I I I I I the Ministry of health and

I I I I I I I I I will evaluate the risks and laying down and

I I I I I I I I I the appropriate measures or even

I I I I I I I I I a special podmínkyke and

I I I I I I I I I to alleviate the identified risks. (I)

I I I I I I I I I shall for products can be even

I I I I I I I I I, grant only if (I)

I I I I I I I I I the request shows that the risks and

I I I I I I I I I it is possible to cut down on even

I I I I I I I I I to an acceptable level. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I


I 8 I I l-Propiconazole {[2-(2,4-dichlorfeny-I 930 g/kg and 1 April 2010 and 31 March 2012 and March 31, 2020 and 8 I relative to the assumptions and

I I I l)-4-propyl-1.3-dioxol-I I I I I I made in reviews and

I I I the an-2-yl] methyl}-lH-1.2-I I I I I I I Department risks

I I I, 4-triazole I I I I I I health in the authorization and

I I I EC No: 262-104-4 I I I I I I stipulates that biocidal and

I I I CAS No: 60207-90-1, I I I I I I the preparation allowed for even

I I I I I I I I I industrial or professional and

I I I I I I I I I use must be used with both

I I I I I I I I I I by appropriate osobnímiochrannými

I I I I I I I I I I work and resources

I I I I I I I I I I, ledažežádost

I I I I I I I I I I the authorisation of the biocidal

I I I I I I I I I of shows that I

I I I I I I I I I the risks for industrial or

I I I I I I I I I expert can

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I given risks to soil and

I I I I I I I I I and the aquatic environment and

I I I I I I I I I the Ministry of health in the

I I I I I I I I I the authorisation shall stipulate that it is even

I I I I I I I I I need to adopt suitable

I I I I I I I I I I risk mitigation measures

I I I I I I I I I I to ochranytěchto

I I I I I I I I I environment. The holder of an authorisation as well as

I I I I I I I I I on labels and/or even

I I I I I I I I I the safety data sheets and

I I I I I I I I I products authorized for

I I I I I I I I I industrial use in particular and

I I I I I I I I I must indicate that freshly and

I I I I I I I I I treated wood must be well

I I I I I I I I I stored under the treatment and

I I I I I I I I I a protective cover or even

I I I I I I I I I impermeable hard bedrock, even

I I I I I I I I I in order to avoid direct and

I I I I I I I I I leaks into the soil or water, and even

I I I I I I I I I the leaking product and

I I I I I I I I I I must shromažďovatpro

I I I I I I I I I reuse or even

I I I I I I I I I for destruction. The Ministry Also

I I I I I I I I I will not allow health and

I I I I I I I I I I nursing products

I I I I I I I I I in situ in the outdoor wood and

I I I I I I I I I environment or for wood, and

I I I I I I I I I which will be exposed and

I I I I I I I I I the weather, unless submitted and

I I I I I I I I I data shows that even

I I I I I I I I I I the product on the basis of

I I I I I I I I I reviews pursuant to section 6 of the

I I I I I I I I I the requirements of § 7 para. 1 to 4 with I

I I I I I I I I I the use of reasonable and

I I I I I I I I I measures to mitigate the risks, and

I I I I I I I I I will if necessary. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I 9 I Difenakum I 3-(3-biphenyl-4-yl-1.2, and 960 g/kg and 1 April 2010 and 31 March 2012 and 31 March 2015 and 14 and due to the fact that effective and

I I I 3.4-tetrahydro-1-naf-I I I I I I the substance is characterized by (I)

I I I tulle]-4-hydroxykumarin I I I I I I as potentially

I I I EC No: 259-978-4 I I I I I I persistent, susceptible to even

I I I CAS No: 56073-07-5 I I I I I I bioaccumulate and toxic, or even

I I I I I I I I I I a very persistent and very

I I I I I I I I I susceptible to bio-accumulate, even

I I I I I I I I I refers to the nipřed and

I I I I I I I I I I restore the inclusion in

I I I I I I I I I of annex a comparative assessment and

I I I I I I I I I the impact in accordance with § 13 and

I I I I I I I I I odst. 7 and 8. (I)

I I I I I I I I I the Ministry of health and

I I I I I I I I I may permit only when I

I I I I I I I I I the following I

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1) nominal concentration and

I I I I I I I I I active substances in preparations and

I I I I I I I I I will not exceed 75 mg/kg

I I I I I I I I I and enables even

I I I I I I I I I I only products intended for

I I I I I I I I I direct use. (I)

I I I I I I I I I 2) containing (I)

I I I I I I I I I aversive substance, possibly even

I I I I I I I I I dye. (I)

I I I I I I I I I 3) products do not apply and

I I I I I I I I I as a tracking powder. (I)

I I I I I I I I I 4) Primary and secondary I

I I I I I I I I I exposure of humans, non-target and

I I I I I I I I I environment I

I I I I I I I I I will be minimized and

I I I I I I I I I through consideration, I

I I I I I I I I I popř. the adoption of all I

I I I I I I I I I and improvement measures

I I I I I I I I I mitigate risk. These include (I)

I I I I I I I I I I, in addition to any other restrictions on use

I I I I I I I I I I only

I I I I I I I I I experts, establish higher and

I I I I I I I I I bounds on the size of the package and even

I I I I I I I I I the determination of obligations and


I I I I I I I I I use for bait

I I I I I I I I I I-resistant safety boxes

I I I I I I I I I tamper. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

10 and K-HDO and cyklohexyl (hydr and 977 g/kg and on July 1, 2010 and June 30, 2012 and June 30, 2020 and 8 as well as the Ministry of health, and

I I I oxy) diazen-l-oxide, I I I I I I I the Ministry of

I I I I I I potassium salt I I I and the Ministry of environment and

I I I no EC: not stated I I I I I I agriculture in the evaluation and

I I I CAS No: 66603-10-9 I I I I I I the application for authorisation and

I I I (this entry includes the I I I I I I a particular product in the I

I I I I I I I hydrated forms I I I accordance with the § 6 and 7hodnotí and

I I I K-HDO) I I I I I I population that can be

I I I I I I I I I exposed his work and I

I I I I I I I I I use, or even

I I I I I I I I I exposure that were not even

I I I I I I I I I presentable represented

I I I I I I I I I I risk assessment

I I I I I I I I I the level of European and

I I I I I I I I I the community, if it is even

I I I I I I I I I needed. The Ministry Also

I I I I I I I I I health in the authorization and

I I I I I I I I I sets out the following as well

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Having regard to the potential risks and

I I I I I I I I I for the environment and

I I I I I I I I I I products workers

I I I I I I I I I to be used in other

I I I I I I I I I than industrial, fully and

I I I I I I I I I automated and

I I I I I I I I I closed systems, unless I

I I I I I I I I I povolenípřípravku I request

I I I I I I I I I shows based on (I)

I I I I I I I I I reviews under section 6, that even

I I I I I I I I I the risk can be reduced to even

I I I I I I I I I I the acceptable level in accordance

I I I I I I I I I s § 7 odst. 1 to 4. (I)

I I I I I I I I I 2. Given the assumptions and

I I I I I I I I I made in reviews and

I I I I I I I I I risks must be products and

I I I I I I I I I used with appropriate and

I I I I I I I I I I personal protective

I I I I I I I I I I, ledažežádost

I I I I I I I I I product authorisation is

I I I I I I I I I on the basis of the assessment referred to in section I

I I I I I I I I I 6, that the risks to the user and

I I I I I I I I I sníženana I may be

I I I I I I I I I the acceptable level for other

I I I I I I I I I ways. (I)

I I I I I I I I I 3. Given the risks for and

I I I I I I I I I is an infant products may not even

I I I I I I I I I use while nursing I

I I I I I I I I I wood, which můžepřijít to the I

I I I I I I I I I direct contact with infants. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And 11 and IPBC and 3-iodo-2-yn-l-yl-I 980 g/kg and 1. July 30, 2010. 30 June 2012. June 2020 and 8 I relative to the assumptions and

I I I N-butylcarbamate I I I I I I made in reviews and

I I I EC No: 259-627-5 I I I I I I I Department risks

I I I CAS No: 55406-53-6 I I I I I I health in the authorization and

I I I I I I I I I products I

I I I I I I I I I allowed for industrial and

I I I I I I I I I and/or professional use shall also

I I I I I I I I I be used with appropriate and

I I I I I I I I I I personal protective

I I I I I I I I I I, ledažežádost

I I I I I I I I I I the authorisation of

I I I I I I I I I shows that risks for even

I I I I I I I I I a/I's industrial neboodborné

I I I I I I I I I user can be reduced and

I I I I I I I I I at an acceptable level and

I I I I I I I I I ways. Taking risks and

I I I I I I I I I to soil and aquatic compartment (I)

I I I I I I I I I the Ministry of health in the

I I I I I I I I I the authorisation shall stipulate that it is even

I I I I I I I I I need to adopt suitable

I I I I I I I I I I risk mitigation measures

I I I I I I I I I I to ochranytěchto

I I I I I I I I I environment. The holder of an authorisation as well as

I I I I I I I I I must indicate on the labels and

I I I I I I I I I and/or in the safety and

I I I I I I I I I I přípravkůpovolených sheets

I I I I I I I I I for industrial use, that even

I I I I I I I I I freshly treated wood must also

I I I I I I I I I be stored even after treatment

I I I I I I I I I under shelter or on and

I I I I I I I I I impermeable hard bedrock, even

I I I I I I I I I in order to avoid direct and

I I I I I I I I I leaks into the soil or water, and even

I I I I I I I I I the leaking product has

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I


I 12 I Chlorofacinon I Chlorofacinon I 978 g/kg and 1. 30 July 2011. 30 June 2013. June 2016 and 14 in view of the risks for both

I I I EC No: 223-003-0 I I I I I I for non-target animals and

I I I the CAS number: 3691-35-8 I I I I I I I předobnovením active substance

I I I I I I I I I I should make its inclusion

I I I I I I I I I a comparative impact assessment and

I I I I I I I I I in accordance with § 13 para. 6 I

I I I I I I I I I písm. b). I

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1) nominal concentration and

I I I I I I I I I active substances in preparations and

I I I I I I I I I other than tracking powder also

I I I I I I I I I will not exceed 50 mg/kg, and enables even

I I I I I I I I I the only pre-engineered and

I I I I I I I I I products. (I)

I I I I I I I I I 2) products that have

I I I I I I I I I use as a tracking and

I I I I I I I I I powder, uvedouna and market

I I I I I I I I I I, subject to the use of trained

I I I I I I I I I. (I)

I I I I I I I I I 3) containing (I)

I I I I I I I I I aversive agent, possibly

I I I I I I I I I dye. (I)

I I I I I I I I I the primary as well as secondary and

I I I I I I I I I exposure of humans, non-target and

I I I I I I I I I environment I

I I I I I I I I I will be minimized and

I I I I I I I I I through consideration, I

I I I I I I I I I popř. the adoption of all I

I I I I I I I I I and improvement measures

I I I I I I I I I mitigate risk. Those are also the

I I I I I I I I I I omezenípoužití, inter alia,

I I I I I I I I I only experts, and

I I I I I I I I I the determination of upper limit and

I I I I I I I I I the size of the packaging and the determination and

I I I I I I I I I I use obligations

I I I I I I I I I bait safety boxes and

I I I I I I I I I a violent and resistant

I I I I I I I I I open. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

13 and Thiabendazole and 2-thiazol-4-yl-I 985 g/kg and 1. July 30, 2010. 30 June 2012. June 2020 and 8 I relative to the assumptions and

I I I I I the lH-benzimidazol I I I I made in reviews and

I I I EC No: 204-725-8 I I I I I I I Department risks

I I I CAS No: 148-79-8 I I I I I I health in the authorization and

I I I I I I I I I preparations for industrial and

I I I I I I I I I and/or professional use

I I I I I I I I I provides that with respect to (I)

I I I I I I I I I double suction and I

I I I I I I I I I I must býtpoužívány a soaking

I I I I I I I I I with appropriate personal and

I I I I I I I I I safety equipment unless I

I I I I I I I I I povolenípřípravku I request

I I I I I I I I I shows that risks for even

I I I I I I I I I a/I's industrial neboodborné

I I I I I I I I I user can be reduced and

I I I I I I I I I at an acceptable level and

I I I I I I I I I ways. (I)

I I I I I I I I I due to the risks and

I I I I I I I I I to soil and aquatic compartment (I)

I I I I I I I I I the Ministry of health in the

I I I I I I I I I the authorisation shall stipulate that it is even

I I I I I I I I I need to adopt suitable

I I I I I I I I I I risk mitigation measures

I I I I I I I I I I to ochranytěchto

I I I I I I I I I environment. The holder of an authorisation as well as

I I I I I I I I I I shall in particular indicate

I I I I I I I I I labels and/or even

I I I I I I I I I the safety data sheets and

I I I I I I I I I products authorized for

I I I I I I I I I industrial use that even

I I I I I I I I I freshly treated wood must also

I I I I I I I I I be stored even after treatment

I I I I I I I I I under shelter or on and

I I I I I I I I I impermeable hard bedrock, even

I I I I I I I I I in order to avoid direct and

I I I I I I I I I leaks into the soil or water, and even

I I I I I I I I I the leaking product has

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I I I I I I I I I the Ministry of health and

I I I I I I I I I will not allow preparations for and

I I I I I I I I I the treatment of wood in place

I I I I I I I I I his outdoor and

I I I I I I I I I environment or for wood, and

I I I I I I I I I which will be exposed and

I I I I I I I I I the weather, unless submitted and

I I I I I I I I I data shows that even

I I I I I I I I I I the product on the basis of

I I I I I I I I I reviews pursuant to section 6 of the

I I I I I I I I I the requirements of § 7 para. 1 to 4 with I

I I I I I I I I I the use of reasonable and

I I I I I I I I I measures to mitigate the risks, and

I I I I I I I I I will if necessary. (I)


I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I 14 and Thiamethoxam thiamethoxam and even 980 g/kg and 1. July 30, 2010. 30 June 2012. June 2020 and 8 I relative to the assumptions and

I I I EC No: 428-650-4 I I I I I I made in reviews and

I I I CAS No: 153719-23-4 I I I I I I I Department risks

I I I I I I I I I health in the authorization and

I I I I I I I I I products I

I I I I I I I I I allowed for industrial and

I I I I I I I I I and/or professional use shall also

I I I I I I I I I be used with appropriate and

I I I I I I I I I I personal protective

I I I I I I I I I I, ledažežádost

I I I I I I I I I I the authorisation of

I I I I I I I I I shows that risks for even

I I I I I I I I I a/I's industrial neboodborné

I I I I I I I I I user can be reduced and

I I I I I I I I I at an acceptable level and

I I I I I I I I I způsoby. (I)

I I I I I I I I I due to the risks and

I I I I I I I I I to soil and aquatic compartment (I)

I I I I I I I I I health in the authorization and

I I I I I I I I I provides that it must be (I)

I I I I I I I I I I take appropriate measures to

I I I I I I I I I for the purpose of risk mitigation and

I I I I I I I I I the protection of the environment. (I)

I I I I I I I I I I, in particular, the authorisation-holder

I I I I I I I I I must indicate on the labels and

I I I I I I I I I and/or in the safety and

I I I I I I I I I I přípravkůpovolených sheets

I I I I I I I I I for industrial use, that even

I I I I I I I I I freshly treated wood must also

I I I I I I I I I be stored even after treatment

I I I I I I I I I under shelter or on and

I I I I I I I I I impermeable hard bedrock, even

I I I I I I I I I in order to avoid direct and

I I I I I I I I I leaks into the soil or water, and even

I I I I I I I I I the leaking product has

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I I I I I I I I I the Ministry of health and

I I I I I I I I I will not allow preparations for and

I I I I I I I I I the treatment of wood in place

I I I I I I I I I his outdoor and

I I I I I I I I I environment or for wood, and

I I I I I I I I I which will be exposed and

I I I I I I I I I the weather, unless submitted and

I I I I I I I I I data shows on the basis of (I)

I I I I I I I I I reviews under section 6, that even

I I I I I I I I I the product meets the requirements of section I

I I I I I I I I I 7 odst. 1 to 4 with and

I I I I I I I I I reasonable measures to

I I I I I I I I I mitigate the risk, if I

I I I I I I I I I necessary. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

15 and the Alpha-I (R)-1, 2-0 (2-2, 2-I 825 g/kg and 1 July 2011 and 30 June 2013 and 30 June 2021 and 14 as well as the Ministry of health, and

I I I Trichloroethyliden)-chloralose I I I I I I I the Ministry of

I I I Alpha-D-glukofuranosa I I I I I I and the Ministry of environment and

I I I EC No: 240-016-7 I I I I I I agriculture in the evaluation and

I I I CAS No: 16222-93-3 I I I I I I the application for authorisation and

I I I I I I I I I in accordance with section 7 (2). 1 to 4

I I I I I I I I I and with annex vyhlášky1 and

I I I I I I I I I evaluated according to the needs and

I I I I I I I I I a specific product and

I I I I I I I I I population that can be

I I I I I I I I I I exposed

I I I I I I I I I the product, and the use or

I I I I I I I I I the exposure scenarios that I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. The Ministry Also

I I I I I I I I I, Ministry of health and

I I I I I I I I I environment and even

I I I I I I I I I the Ministry of agriculture and

I I I I I I I I I the grant of authorisation of the product and

I I I I I I I I I will assess the risk of further and

I I I I I I I I I shall ensure that I was accepted

I I I I I I I I I the appropriate measures or even

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. Permits for even

I I I I I I I I I I can only grant products

I I I I I I I I I if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. Přípravkynesmí also be

I I I I I I I I I allowed in particular for I

I I I I I I I I I outdoor use if (I)

I I I I I I I I I I do not předloženyúdaje

I I I I I I I I I, proving that the medicine I

I I I I I I I I I satisfies požadavkypodle, paragraph 7, and

I I I I I I I I I odst. 1 to 4 in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to


I I I I I I I I I mitigate the risk, if I

I I I I I I I I I necessary. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1) nominal concentration and

I I I I I I I I I active substances in preparations and

I I I I I I I I I shall not exceed 40 g/kg. (I)

I I I I I I I I I 2) containing (I)

I I I I I I I I I aversive činidloa dye. (I)

I I I I I I I I I 3) will be povolenypouze and

I I I I I I I I I preparations for use in (I)

I I I I I I I I I closed for security and

I I I I I I I I I I the bait boxes

I I I I I I I I I a violent and resistant

I I I I I I I I I open. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I 17 I Bromadiolon I [3-(4 '-brombifenyl-4-(I) 969 g/kg and 1 July 2011 and 30 June 2013 and 30 June 2016 and 14 as well as due to the účinnélátce and

I I I-l-yl) phenyl-3-hydroxy-I I I I I I I a

I I I-hydroxy propyl]-2 h-I I I I I I potentially persistent, and

I I I chromen-2-on I I I I I I liable to bioaccumulate and

I I I EC No: 249-205-9 I I I I I I toxic or very well

I I I CAS No: 28772-56-7 I I I I I I I persistent and very

I I I I I I I I I liable to bioaccumulate,

I I I I I I I I I at her before resuming her even

I I I I I I I I I inclusion in annex also covers

I I I I I I I I I a comparative impact assessment and

I I I I I I I I I in accordance with § 13 para. 6 I

I I I I I I I I I písm. b). I

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1) nominal concentration and

I I I I I I I I I active substances in preparations and

I I I I I I I I I will not exceed 50 mg/kg

I I I I I I I I I and enables even

I I I I I I I I I only pre-engineered and

I I I I I I I I I products. (I)

I I I I I I I I I 2) containing (I)

I I I I I I I I I aversive agent, possibly

I I I I I I I I I dye. (I)

I I I I I I I I I 3) products do not apply and

I I I I I I I I I as a tracking powder. (I)

I I I I I I I I I the primary as well as secondary and

I I I I I I I I I exposure of humans, non-target and

I I I I I I I I I environment I

I I I I I I I I I will be minimized and

I I I I I I I I I I, through the consideration and

I I I I I I I I I the adoption of all appropriate and

I I I I I I I I I and improvement measures

I I I I I I I I I mitigate risk. These include (I)

I I I I I I I I I I, in addition to any other restrictions on use

I I I I I I I I I I only

I I I I I I I I I experts, establish higher and

I I I I I I I I I bounds on the size of the package and even

I I I I I I I I I the determination of obligations and

I I I I I I I I I use for bait

I I I I I I I I I I-resistant safety boxes

I I I I I I I I I tamper. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And even 18 Thiacloprid and {(Z)-3-[(6-chloro-and 975 g/kg on 1 January 2010 and is not listed as December 31, 2019, and 8 as well as the Ministry of health, and

I I I 3-pyridyl) methyl]-I I I I I I I the Ministry of

I I I l, 3-thiazolidin-2-I I I I I I and the Ministry of environment and

I I I I I cyanamide ylidene} I I I I agriculture in the evaluation and

I I I no EC: not stated I I I I I I the application for authorisation and

I I I CAS No: 111988-49-9 I I I I I I in accordance with section 7 (2). 1 to 4

I I I I I I I I I and with annex vyhlášky1 and

I I I I I I I I I evaluated according to the needs and

I I I I I I I I I a specific product and

I I I I I I I I I population that can be

I I I I I I I I I I exposed

I I I I I I I I I the product, and the use or

I I I I I I I I I the exposure scenarios that I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. The Ministry Also

I I I I I I I I I I in granting health

I I I I I I I I I I will evaluate the product authorisation

I I I I I I I I I the risks and ensure that

I I I I I I I I I was accepted the appropriate measures and

I I I I I I I I I or special even

I I I I I I I I I I to alleviate the conditions

I I I I I I I I I the identified risks. Authorisation As Well As

I I I I I I I I I I for lzeudělit products

I I I I I I I I I only if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Given the assumptions and

I I I I I I I I I made in reviews and

I I I I I I I I I risk products authorised

I I I I I I I I I for industrial and/or

I I I I I I I I I professional use must also be


I I I I I I I I I used with appropriate and

I I I I I I I I I I personal protective

I I I I I I I I I I, ledažežádost

I I I I I I I I I I the authorisation of

I I I I I I I I I shows that risks for even

I I I I I I I I I a/I's industrial neboodborné

I I I I I I I I I user can be reduced and

I I I I I I I I I at an acceptable level and

I I I I I I I I I ways. (I)

I I I I I I I I I 2. Given the risks for and

I I I I I I I I I the soil and water environment is even

I I I I I I I I I need to adopt suitable

I I I I I I I I I measures to mitigate the risks and

I I I I I I I I I I to ochranytěchto

I I I I I I I I I environment. Štítkya/or

I I I I I I I I I material safety data sheets and products

I I I I I I I I I allowed for industrial and

I I I I I I I I I use, in particular, must indicate, even

I I I I I I I I I I freshly treated wood

I I I I I I I I I I after treatment must be

I I I I I I I I I stored under the protective and

I I I I I I I I I cover and/or even

I I I I I I I I I impermeable hard bedrock, even

I I I I I I I I I in order to avoid direct and

I I I I I I I I I leaks into the soil or water, and even

I I I I I I I I I the leaking product has

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I I I I I I I I I 3. In addition, the products may not even

I I I I I I I I I be allowed for curing and

I I I I I I I I I wood in the place of its use in the I

I I I I I I I I I near water, in which I

I I I I I I I I I cannot prevent the direct and

I I I I I I I I I penetration into water and

I I I I I I I I I environment, or for wood, and

I I I I I I I I I which will be in contact with and

I I I I I I I I I surface water, unless I

I I I I I I I I I submitted data demonstrate, even

I I I I I I I I I that the product meets and

I I I I I I I I I the requirements pursuant to § 7 para. 1 I

I I I I I I I I I to 4 and in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to (I)

I I I I I I I I I mitigate risk, if I

I I I I I I I I I necessary. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

Also 19 and also the reaction mixture and Indoxacarb 796 g/kg and 1. January 1, 2010 and is listed as 31. December 2019 and 18 as well as the Ministry of health, and

I I I the reaction mixture (methyl-(4aS)-and I I I I I I I the Ministry of

I I (S) and enantiomers of methyl-(4aR)-7-chloro-2-I I I I I I and the Ministry of environment and

And (I) and (R) in the ratio of I-{(methoxykarbonyl) [4-I I I I I I agriculture in the evaluation and

I I 75:25) I (trifluormethoxy) I I I I I I the application for authorisation and

I I I phenyl] karbamoyl}-2.3, I I I I I I in accordance with section 7 (2). 1 to 4

I I I, 4a, 5-tetrahydroindeno I I I I I I and with annex vyhlášky1 and

I I I [1.2-e] [l, 3.4] oxa-I I I I I I evaluated according to the needs and

I I I diazin4a-carboxylate forms I I I I I I a specific product and

I I I (this includes the I I I I I I population that can be

I I I the reaction mixture I I I I I I I exposed

I I I molecules (S) and (R) in the I I I I I I the product, and the use or

I I I the ratio of 75:25) I I I I I I the exposure scenarios that I

I I I no EC: not stated I I I I I I I have been presentable

I I I CAS No: enantiomer (S): I I I I I I represented in the evaluation and

I I I 173584-44-6 and I I I I I I I-level risk

I I I enantiomer (R): I I I I I I the community. The Ministry Also

I I I 185608-75-7) I I I I I I I in granting health

I I I I I I I I I I will evaluate the product authorisation

I I I I I I I I I the risks and ensure that

I I I I I I I I I was accepted the appropriate measures and

I I I I I I I I I or special even

I I I I I I I I I I to alleviate the conditions

I I I I I I I I I the identified risks. Authorisation As Well As

I I I I I I I I I for preparations can also be

I I I I I I I I I, grant only if (I)

I I I I I I I I I the request shows that the risks and

I I I I I I I I I it is possible to cut down on even

I I I I I I I I I to an acceptable level. The Holder And The

I I I I I I I I I authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I I should be přijmoutvhodná

I I I I I I I I I measures to mitigate the risks, and

I I I I I I I I I to reduce the naminimum and

I I I I I I I I I the potential exposure of people, and

I I I I I I I I I non-target species and water and

I I I I I I I I I environment. Štítkya/or

I I I I I I I I I I safety data sheets

I I I I I I I I I authorised products must also

I I I I I I I I I in particular indicate that: (I)

I I I I I I I I I 1. Products may not be

I I I I I I I I I placed in places and

I I I I I I I I I available for infants, children and

I I I I I I I I I and pets. (I)

I I I I I I I I I 2. Products may not be

I I I I I I I I I placed near the external and

I I I I I I I I I drain. (I)


I I I I I I I I I 3. Unused products must also

I I I I I I I I I be properly disposed of and even

I I I I I I I I I must not be emitted into and

I I I I I I I I I drain. (I)

I I I I I I I I I for non-professional use

I I I I I I I I I I only are allowed

I I I I I I I I I I prepared to

I I I I I I I I I use. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

20 and Aluminium phosphide and Aluminium phosphide and 830 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I) 14 and the Ministry of health, and

And even a relaxing and EC No: 244-088-0 I I I I I I I the Ministry of

I I I fosfin CAS No: 20859-73-8 I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for authorisation and

I I I I I I I I I in accordance with section 7 (2). 1 to 4

I I I I I I I I I and with annex vyhlášky1 and

I I I I I I I I I evaluated according to the needs and

I I I I I I I I I a specific product and

I I I I I I I I I population that can be

I I I I I I I I I I exposed

I I I I I I I I I the product, and the use or

I I I I I I I I I the exposure scenarios that I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. The Ministry Also

I I I I I I I I I I in granting health

I I I I I I I I I I will evaluate the product authorisation

I I I I I I I I I the risks and ensure that

I I I I I I I I I was accepted the appropriate measures and

I I I I I I I I I or special even

I I I I I I I I I I to alleviate the conditions

I I I I I I I I I the identified risks. Authorisation As Well As

I I I I I I I I I I for lzeudělit products

I I I I I I I I I only if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. Přípravkynelze I

I I I I I I I I I allow in particular for use and

I I I I I I I I I in indoor areas, and

I I I I I I I I I if they are not accompanied by the particulars and

I I I I I I I I I, proving that the medicine I

I I I I I I I I I satisfies požadavkypodle, paragraph 7, and

I I I I I I I I I odst. 1 to 4 and in annex I

I I I I I I I I I vyhlášky1, possibly with even

I I I I I I I I I and

I I I I I I I I I reasonable measures to (I)

I I I I I I I I I mitigate risk, if I

I I I I I I I I I necessary. Držitelpovolení I

I I I I I I I I I will fulfil the following conditions: (I)

I I I I I I I I I Preparations may also sell

I I I I I I I I I only trained professionals and even

I I I I I I I I I používányrovněž I may be

I I I I I I I I I only trained experts. (I)

I I I I I I I I I 1), given the observed and

I I I I I I I I I the risks for the user must

I I I I I I I I I be suitable

I I I I I I I I I measures to mitigate the risks. (I)

I I I I I I I I I I, these measures include

I I I I I I I I I the use of appropriate personal and

I I I I I I I I I protective gear, as well as

I I I I I I I I I use applicators and even

I I I I I I I I I presentation of the I

I I I I I I I I I the form of exposure and

I I I I I I I I I a user to an acceptable and

I I I I I I I I I úroveň. (I)

I I I I I I I I I 2) given the observed and

I I I I I I I I I the risks for terrestrial and

I I I I I I I I I non-target species must be

I I I I I I I I I applied appropriate measures to (I)

I I I I I I I I I mitigate risk. Between this and the

I I I I I I I I I measures include non-application and

I I I I I I I I I in places where I

I I I I I I I I I found the mammals living in the I

I I I I I I I I I holes other than the target and

I I I I I I I I I druhy. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And 21 and fenpropimorph I (+/-cis-4-[3-(4-(I) 930 g/kg and 1 July 2011 and 30 June 2013 and 30 June 2021 and 8 as well as the Ministry of health, and

I I I tert-butylfenyl)-I I I I I I I the Ministry of

I I I 2-trimethylsilyl]-2.6-I I I I I I and the Ministry of environment and

Dimethylmorfolin I I I I I I I I I agriculture in the evaluation and

I I I EC No: 266-719-9 I I I I I I the application for and

I I I the CAS number: 67564-91-4 I I I I I I preparations in accordance with article 7 and

I I I I I I I I I, paragraphs 1 to 4 and annex I,

I I I I I I I I I vyhlášky1 hodnotív case, even

I I I I I I I I I it's for danýpřípravek and

I I I I I I I I I I it relevant exposure scenario

I I I I I I I I I and the population, which may be

I I I I I I I I I exposed product, if I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. Přiudílení I


I I I I I I I I I I the authorisation of

I I I I I I I I I the Ministry of health, and

I I I I I I I I I I the Ministry of

I I I I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture will evaluate the risks and

I I I I I I I I I and further ensure that was even

I I I I I I I I I the appropriate measures taken or

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. Permits for even

I I I I I I I I I I can only grant products

I I I I I I I I I if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Given the assumptions and

I I I I I I I I I made in reviews and

I I I I I I I I I risks must be products and

I I I I I I I I I used with the relevant and

I I I I I I I I I I personal protective

I I I I I I I I I resources, unless I request

I I I I I I I I I I the authorisation of

I I I I I I I I I shows that risks for even

I I I I I I I I I industrial users can also

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I 2. Given the risks for and

I I I I I I I I I the soil and water environment is even

I I I I I I I I I need to adopt suitable

I I I I I I I I I I risk mitigation measures

I I I I I I I I I I to ochranytěchto

I I I I I I I I I environment. Štítkya/or

I I I I I I I I I material safety data sheets and products

I I I I I I I I I allowed for industrial and

I I I I I I I I I use, in particular, must indicate, even

I I I I I I I I I I freshly treated wood

I I I I I I I I I I after treatment must be

I I I I I I I I I stored under the protective and

I I I I I I I I I cover or on impermeable and

I I I I I I I I I hard bedrock, so that

I I I I I I I I I avoid direct spills and

I I I I I I I I I soil or water, and that is also

I I I I I I I I I leaking product has

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And even the 22 boric acid and boric acid and 990 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I), 8 (I) the Ministry of health, and

I I I EC No: 233-139-2 I I I I I I I the Ministry of

I I I the CAS number: 10043-35-3 I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for authorisation and

I I I I I I I I I in accordance with section 7 (2). 1 to 4

I I I I I I I I I and with annex vyhlášky1 and

I I I I I I I I I evaluated according to the needs and

I I I I I I I I I a specific product and

I I I I I I I I I population that can be

I I I I I I I I I exposed to the product, even

I I I I I I I I I and use or even

I I I I I I I I I exposure that were not even

I I I I I I I I I presentable represented

I I I I I I I I I I risk assessment

I I I I I I I I I. When Both The

I I I I I I I I I the granting of authorisation and

I I I I I I I I I the Ministry of health, and

I I I I I I I I I I the Ministry of

I I I I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture will evaluate the risks and

I I I I I I I I I and further ensure that was even

I I I I I I I I I the appropriate measures taken or

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. Permits for even

I I I I I I I I I I can only grant products

I I I I I I I I I if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1) Preparations authorized for even

I I I I I I I I I I industrial and professional

I I I I I I I I I use must be used

I I I I I I I I I with the relevant personal and

I I I I I I I I I I trade resources

I I I I I I I I I unless the application for authorisation and

I I I I I I I I I of shows that I

I I I I I I I I I the risks for industrial and/or

I I I I I I I I I support uživatelemohou be

I I I I I I I I I reduced to acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I 2) due to the risks and

I I I I I I I I I the soil and water environment

I I I I I I I I I I cannot be


I I I I I I I I I allowed for the treatment and

I I I I I I I I I wood at the site of its use and

I I I I I I I I I in the outdoor environment or even

I I I I I I I I I for wood that will be

I I I I I I I I I exposed to weather, and

I I I I I I I I I unless I předloženéúdaje

I I I I I I I I I demonstrate that I

I I I I I I I I I will fulfil the requirements referred to in section 7 (I)

I I I I I I I I I odst. 1 to 4 and in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to

I I I I I I I I I mitigate the risk. In Particular, I

I I I I I I I I I labels and/or safety and

I I I I I I I I I leaves products authorized and

I I I I I I I I I for industrial use

I I I I I I I I I indicate that freshly treated and

I I I I I I I I I the wood must be poošetření and

I I I I I I I I I stored under a glazed roof and

I I I I I I I I I cover or on impermeable and

I I I I I I I I I hard bedrock, so that

I I I I I I I I I prevent direct losses to the I

I I I I I I I I I land, and that it is leaking and

I I I I I I I I I must collect and

I I I I I I I I I for reuse or even

I I I I I I I I I for destruction. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

And 23 as well as boron trioxide and boron trioxide and 975 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I), 8 (I) the Ministry of health, and

I I I EC No: 214-125-8 I I I I I I I the Ministry of

I I I CAS No: 1303-86-2 I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for authorisation and

I I I I I I I I I in accordance with article I, paragraph 7,

I I I I I I I I I odst. 1 to 4 and annex I,

I I I I I I I I I hodnotípodle I vyhlášky1

I I I I I I I I I for the particular needs and

I I I I I I I I I the product stocks that I

I I I I I I I I I can be subjected to (I)

I I I I I I I I I a product, and the use or

I I I I I I I I I the exposure scenarios that I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. Přiudílení I

I I I I I I I I I I the authorisation of

I I I I I I I I I the Ministry of health, and

I I I I I I I I I I the Ministry of

I I I I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture will evaluate the risks and

I I I I I I I I I and further ensure that was even

I I I I I I I I I the appropriate measures taken or

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. (I)

I I I I I I I I I shall for products can be even

I I I I I I I I I, grant only if (I)

I I I I I I I I I the request shows that the risks and

I I I I I I I I I it is possible to cut down on even

I I I I I I I I I to an acceptable level. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Preparations allowed for even

I I I I I I I I I industrial and professional use

I I I I I I I I I I must be used with

I I I I I I I I I the relevant personal and

I I I I I I I I I I trade resources

I I I I I I I I I unless the application for authorisation and

I I I I I I I I I of shows that I

I I I I I I I I I the risks for industrial and/or

I I I I I I I I I support uživatelemohou be

I I I I I I I I I reduced to acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I 2. Given the risks for and

I I I I I I I I I the soil and water environment

I I I I I I I I I I cannot be

I I I I I I I I I allowed for the treatment and

I I I I I I I I I wood at the site of its use and

I I I I I I I I I in the outdoor environment or even

I I I I I I I I I for wood that will be

I I I I I I I I I exposed to weather, and

I I I I I I I I I unless I předloženéúdaje

I I I I I I I I I demonstrate that I

I I I I I I I I I will fulfil the requirements referred to in section 7 (I)

I I I I I I I I I odst. 1 to 4 and in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to

I I I I I I I I I mitigate the risk. In Particular, I

I I I I I I I I I labels and/or safety and

I I I I I I I I I leaves products authorized and

I I I I I I I I I for industrial use

I I I I I I I I I indicate that freshly treated and

I I I I I I I I I the wood must be poošetření and

I I I I I I I I I stored under a glazed roof and

I I I I I I I I I cover or on impermeable and

I I I I I I I I I hard bedrock, so that


I I I I I I I I I prevent direct losses to the I

I I I I I I I I I land, and that it is leaking and

I I I I I I I I I must collect and

I I I I I I I I I for reuse or even

I I I I I I I I I for destruction. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

24 I tetraboritan I tetraboritan disodium as well as 990 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I), 8 (I) the Ministry of health, and

And disodium and EC No: 214-540-4 I I I I I I I the Ministry of

I I I the CAS number (anhydrous) I I I I I I and the Ministry of environment and

I I I 1330-43-4 I I I I I I agriculture in the evaluation and

I I I the CAS number (pentahydrate) I I I I I I the application for and

I I I 12271-73-1, I I I I I I preparations in accordance with article 7 and

I I I CAS (dekahydrát) I I I I I I (2) 1 to 4 and annex I,

I I I 1303-96-4 I I I I I I vyhlášky1 hodnotív case, even

I I I I I I I I I it's for danýpřípravek and

I I I I I I I I I I it relevant exposure scenario

I I I I I I I I I and the population, which may be

I I I I I I I I I exposed product, if I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and

I I I I I I I I I I-level risk

I I I I I I I I I The Community. The Ministry Also

I I I I I I I I I, Ministry of health and

I I I I I I I I I environment and even

I I I I I I I I I the Ministry of agriculture and

I I I I I I I I I the grant of authorizations for the I

I I I I I I I I I will evaluate the risks, and even product

I I I I I I I I I shall further ensure sub-region I

I I I I I I I I I the appropriate measures taken or

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. Permits for even

I I I I I I I I I I can only grant products

I I I I I I I I I if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. The holder of an authorisation as well as

I I I I I I I I I will fulfil the following conditions: (I)

I I I I I I I I I 1) Preparations authorized for even

I I I I I I I I I a/I's industrial neboodborné

I I I I I I I I I use must be used with I

I I I I I I I I I the relevant personal and

I I I I I I I I I I trade resources

I I I I I I I I I unless the application for authorisation and

I I I I I I I I I of shows that I

I I I I I I I I I the risks for industrial and/or

I I I I I I I I I support uživatelemohou be

I I I I I I I I I reduced to acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I 2) due to the risks and

I I I I I I I I I the soil and water environment

I I I I I I I I I in addition preparations cannot be and

I I I I I I I I I allowed for the treatment and

I I I I I I I I I wood at the site of its use and

I I I I I I I I I in the outdoor environment or even

I I I I I I I I I for wood that will be

I I I I I I I I I exposed to weather, and

I I I I I I I I I unless I předloženéúdaje

I I I I I I I I I demonstrate that I

I I I I I I I I I will fulfil the requirements referred to in section 7 (I)

I I I I I I I I I odst. 1 to 4 and in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to

I I I I I I I I I mitigate the risk, if I

I I I I I I I I I necessary. Zejménaštítky I

I I I I I I I I I and/or material safety data sheets and

I I I I I I I I I products authorized for

I I I I I I I I I industrial use indicate, even

I I I I I I I I I I freshly treated wood

I I I I I I I I I I after treatment must be

I I I I I I I I I stored on sheltered and

I I I I I I I I I and/or impermeable hard and

I I I I I I I I I the subsoil in order to prevent and

I I I I I I I I I a direct loss of dopůdy, and that

I I I I I I I I I the leaking product must also

I I I I I I I I I I collected for reuse

I I I I I I I I I use or disposal. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I even oktaboritan and oktaboritan 25 disodium and 975 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I), 8 (I) the Ministry of health, and

I I I I I disodium tetrahydrate I I I I I the Ministry of

I I I no EC tetrahydrate: 234-541-0 I I I I I I and the Ministry of environment and

I I I the CAS number: 12283-03-4 I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for authorisation and

I I I I I I I I I in accordance with section 7 (2). 1 to 4

I I I I I I I I I and annex vyhlášky1 assesses and

I I I I I I I I I I, as appropriate for the particular

I I I I I I I I I the product stocks that I

I I I I I I I I I can be subjected to (I)

I I I I I I I I I a product, and the use or

I I I I I I I I I the exposure scenarios that I

I I I I I I I I I I have been presentable

I I I I I I I I I represented in the evaluation and


I I I I I I I I I I-level risk

I I I I I I I I I The Community. Přiudílení I

I I I I I I I I I I the authorisation of

I I I I I I I I I the Ministry of health, and

I I I I I I I I I I the Ministry of

I I I I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture will evaluate the risks and

I I I I I I I I I and further ensure that was even

I I I I I I I I I the appropriate measures taken or

I I I I I I I I I set out specific conditions and

I I I I I I I I I to alleviate the identified and

I I I I I I I I I rizik. Permits for even

I I I I I I I I I I can only grant products

I I I I I I I I I if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. The holder of an authorisation as well as

I I I I I I I I I will fulfil the following conditions: (I)

I I I I I I I I I 1) Preparations approved for even

I I I I I I I I I industrial and professional use

I I I I I I I I I I must be used with

I I I I I I I I I the relevant personal and

I I I I I I I I I I trade resources

I I I I I I I I I unless the application for authorisation and

I I I I I I I I I of shows that I

I I I I I I I I I the risks for industrial and/or

I I I I I I I I I support uživatelemohou be

I I I I I I I I I reduced to acceptable and

I I I I I I I I I level in other ways. (I)

I I I I I I I I I 2) due to the risks and

I I I I I I I I I the soil and water environment

I I I I I I I I I I cannot be

I I I I I I I I I allowed for the treatment and

I I I I I I I I I wood at the site of its use and

I I I I I I I I I in the outdoor environment or even

I I I I I I I I I for wood that will be

I I I I I I I I I exposed to weather, and

I I I I I I I I I unless I předloženéúdaje

I I I I I I I I I demonstrate that I

I I I I I I I I I will fulfil the requirements referred to in section 7 (I)

I I I I I I I I I, paragraph 1 to 4 and in annex I

I I I I I I I I I vyhlášky1 with and

I I I I I I I I I reasonable measures to

I I I I I I I I I mitigate the risk. In Particular, I

I I I I I I I I I labels and/or safety and

I I I I I I I I I leaves products authorized and

I I I I I I I I I for industrial use

I I I I I I I I I indicate that freshly treated and

I I I I I I I I I the wood must be poošetření and

I I I I I I I I I stored under a glazed roof and

I I I I I I I I I cover or on impermeable and

I I I I I I I I I hard bedrock, so that

I I I I I I I I I prevent direct losses to the I

I I I I I I I I I land, and that it is leaking and

I I I I I I I I I must collect and

I I I I I I I I I for reuse or even

I I I I I I I I I I disposal

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

Even 27 and Nitrogen and Nitrogen and 999 g/kg and 1. September 2011 and 31. August 2013 and 31. August 2021 (I) 18 and the Ministry of health, and

I I I EC No: 231-783-9 I I I I I I I the Ministry of

I I I the CAS number: 7727-37-9 I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture in the evaluation and

I I I I I I I I I the application for and

I I I I I I I I I preparations in accordance with article 7 and

I I I I I I I I I odst. 1 to 4 and annex I

I I I I I I I I I vyhlášky1 hodnotív case, even

I I I I I I I I I it's for danýpřípravek and

I I I I I I I I I relevant population that even

I I I I I I I I I may be issued

I I I I I I I I I the product, and the use or

I I I I I I I I I the exposure scenarios that were not even

I I I I I I I I I presentable taken into account

I I I I I I I I I I risk assessment

I I I I I I I I I. (I)

I I I I I I I I I the Ministry of health, and

I I I I I I I I I I the Ministry of

I I I I I I I I I and the Ministry of environment and

I I I I I I I I I agriculture grant and

I I I I I I I I I I will evaluate the product authorisation

I I I I I I I I I the risks and ensure that

I I I I I I I I I was accepted the appropriate measures and

I I I I I I I I I or special even

I I I I I I I I I I to alleviate the conditions

I I I I I I I I I the identified risks. Authorisation As Well As

I I I I I I I I I I for lzeudělit products

I I I I I I I I I only if the request

I I I I I I I I I shows that the risk is

I I I I I I I I I be reduced to an acceptable and

I I I I I I I I I úroveň. (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Preparations may also sell

I I I I I I I I I only trained professionals and even

I I I I I I I I I používányrovněž I may be


I I I I I I I I I only trained experts. (I)

I I I I I I I I I 2. In order to minimize and

I I I I I I I I I the risks must be implemented even

I I I I I I I I I-safe pracovnípostupy and I

I I I I I I I I I security systems work, as well as

I I I I I I I I I, including availability, if any, and

I I I I I I I I I I the personal protective

I I I I I I I I I resources. (I)

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I

I even kumatetralyl and kumatetralyl 28 and 980 g/kg and 1. 30 July 2011. 30 June 2013. June 2016 and 14 as well as due to the identified and

I I I the EC number: 227-424-0 I I I I I I the risks for non-target animals and

I I I the CAS number: 5836-29-3 I I I I I I for active substances prior to and

I I I I I I I I I I restore the inclusion in

I I I I I I I I I of the annex should also be carried out

I I I I I I I I I a comparative risk assessment and

I I I I I I I I I according to § 13 para. 6 (a). (I)

I I I I I I I I I b). (I)

I I I I I I I I I the holder of the authorisation shall comply with these and

I I I I I I I I I the conditions: (I)

I I I I I I I I I 1. Nominal concentration and

I I I I I I I I I active substances in preparations and

I I I I I I I I I other than tracking powder also

I I I I I I I I I will not exceed 375 mg/kg and

I I I I I I I I I I only allow

I I I I I I I I I canned products. (I)

I I I I I I I I I 2. products include

I I I I I I I I I aversive ingredient. (I)

I I I I I I I I I dye. (I)

I I I I I I I I I 3. primary and secondary I

I I I I I I I I I exposure of humans, non-target and

I I I I I I I I I environment I

I I I I I I I I I will minimize and weighing

I I I I I I I I I popř. the adoption of any

I I I I I I I I I the appropriate and available

I I I I I I I I I measures to mitigate the risks. (I)

I I I I I I I I I That include but not limited to (I)

I I I I I I I I I limit the use of and

I I I I I I I I I only specialists, establishing and

I I I I I I I I I the upper limit of the size and

I I I I I I I I I pack and the determination and

I I I I I I I I I the obligation to apply for and

I I I I I I I I I bait safety boxes and

I I I I I I I I I a violent and resistant

I I I I I I I I I open. " I

I-------I-----------------I-------------------------I----------I-------------------I-------------------I-------------------I---------------I------------------------------I



Article. (II)



The effectiveness of the



This Act shall take effect on the date of its publication.



Vaidya in the r.



Klaus r.



Fischer v. r.

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