委员会实施条例(EU) No 1134/2011,根据欧洲议会和理事会条例(EC) No 1107/2009(该条例关于市场上出售植物保护产品)不继续批准活性物质吲哚酮草酯,以及修订委员会实施条例(EU) No 540/2011?(1)

技术法规类型:欧盟Eurlex法规 来源:tbtmap

EURLEX ID:32011R1134

OJ编号:OJ L 292, 10.11.2011, p. 1-3

中文标题:委员会实施条例(EU) No 1134/2011,根据欧洲议会和理事会条例(EC) No 1107/2009(该条例关于市场上出售植物保护产品)不继续批准活性物质吲哚酮草酯,以及修订委员会实施条例(EU) No 540/2011?(1)

原文标题:Commission Implementing Regulation (EU) No 1134/2011 of 9 November 2011 concerning the non-renewal of the approval of the active substance cinidon-ethyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011 (1)

分类:03.50.20_植物健康

文件类型:二级立法 Regulation|条例

生效日期:2011-11-30

废止日期:2058-12-31

法规全文:查看欧盟官方文件

HTML PUBLIC "-//W3C//DTD HTML 4.01 Transitional//EN"EN
10.11.2011 Official
Journal
of
the
European
Union
L
292/1
II
(Non-legislative acts)
REGULATIONS
COMMISSION IMPLEMENTING REGULATION (EU) No 1134/2011
of 9 November 2011
concerning the non-renewal of the approval of the active substance cinidon-ethyl, in accordance
with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the
placing of plant protection products on the market, and amending Commission Implementing
Regulation (EU) No 540/2011
(Text with EEA relevance)
THE EUROPEAN COMMISSION,
Annex to Commission Implementing Regulation (EU) No
540/2011 of 25 May 2011 implementing Regulation
(EC) No 1107/2009 of the European Parliament and of
the Council as regards the list of approved active
Having regard to the Treaty on the Functioning of the European
substances ( 4 ) and is to be deemed to have been
Union,
approved under Regulation (EC) No 1107/2009.
Having regard to Regulation (EC) No 1107/2009 of the
European Parliament and of the Council of 21 October 2009
(4) The
Commission
did
not,
however,
receive
any
appli
concerning the placing of plant protection products on the
cations for the active substance concerned and the time
market and repealing Council Directives 79/117/EEC and
period for the submission of such applications, as
91/414/EEC (
provided for in Article 4(1) of Commission Regulation

1 ), and in particular Article 20 thereof,
(EU) No 1141/2010 of 7 December 2010 laying down
the procedure for the renewal of the inclusion of a
second group of active substances in Annex I to
Whereas:
Council Directive 91/414/EEC and establishing the list
of those substances ( 5 ), has expired.
(1) The
active
substance
cinidon-ethyl
was
included
in
Annex I to Council Directive 91/414/EEC of 15 July
1991 concerning the placing of plant protection
(5) Consequently,
the
approval
of
that
active
substance
products on the market (
should not be renewed and it should be removed from

2 ) for a period expiring on
30 September 2012.
Part A of the Annex to Implementing Regulation (EU)

No 540/2011, as from the date on which its approval
would have expired had it not been extended by
Directive 2010/77/EU.
(2) To
enable
applicants
to
prepare
their
applications
and
to
enable the Commission to evaluate and decide upon such
applications, that inclusion was extended until
31 December 2015 by Commission Directive
(6) This
Regulation
does
not
prejudice
the
submission
of
an
2010/77/EU of 10 November 2010 amending Council
application for this substance pursuant to Article 7 of
Directive 91/414/EEC as regards the expiry dates for
Regulation (EC) No 1107/2009.
inclusion in Annex I of certain active substances ( 3 ).
(3) In
accordance
with
Article
78(3)
of
Regulation
(EC)
No (7) The
measures
provided
for
in
this
Regulation
are
in
1107/2009 that substance was included in Part A of the
accordance with the opinion of the Standing
Committee on the Food Chain and Animal Health,
( 1 ) OJ L 309, 24.11.2009, p. 1.
( 2 ) OJ L 230, 19.8.1991, p. 1.
( 4 ) OJ L 153, 11.6.2011, p. 1.
( 3 ) OJ L 293, 11.11.2010, p. 48.
( 5 ) OJ L 322, 8.12.2010, p. 10.

L 292/2
EN
Official Journal of the European Union
10.11.2011
HAS ADOPTED THIS REGULATION:
Article 3
Article 1
Amendments to Implementing Regulation (EU) No
540/2011
Non-renewal of approval
Part A of the Annex to Implementing Regulation (EU) No
The approval of the active substance cinidon-ethyl is not
540/2011 is amended in accordance with the Annex to this
renewed.
Regulation.
Article 2
Grace periods
Any grace period granted by a Member State for plant
Article 4
protection products containing cinidon-ethyl shall expire on
Entry into force
31 March 2013 at the latest for the sale and distribution and
on 31 March 2014 at the latest for the disposal, storage, and
This Regulation shall enter into force on the 20th day following
use of existing stocks.
its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 9 November 2011.
For the Commission
The President
José Manuel BARROSO

10.11.2011 Off
ANNEX
In Part A of the Annex to Implementing Regulation (EU) No 540/2011, row 33 is replaced by the following:
Number
Common name,
identification numbers
IUPAC name Purity
(1 ) Date
of
approval Expiration
of
approval Specific
provisions
EN
‘33 Cinidon-ethyl
(Z)-ethyl 2-chloro-3- 940 g/kg 1
October
2002 30
September
2012 Only
uses
as
herbicide
may
be
authorised.

[2-chloro-5-(cyclohex-
CAS No 142891-20-1 1-ene-1,2-dicar
For the implementation of the uniform principles as referred to in Article 29(6) of
Regulation (EC) No 1107/2009, the conclusions of the review report on cinidon-
CIPAC No 598
boximido)phenyl]
acrylate
ethyl, and in particular Appendices I and II thereof, as finalised in the Standing
Committee on the Food Chain and Animal Health on 19 April 2002 shall be
taken into account. In this overall assessment Member States:
— should pay particular attention to the potential for ground water contamination,
when the active substance is applied in regions with vulnerable soil (e.g. soils with
neutral or high pH values) and/or climatic conditions,
— should pay particular attention to the protection of aquatic organisms.
icial
Conditions of authorisation must include risk mitigation measures, where appro
Jour
priate.’
nal
(1 ) Further details on identity and specification of active substances are provided in their review reports.
of
the
European
Union
L
292/3

附件:

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