http://www.legislation.gov.uk/id/eudn/2020/2182

Commission Implementing Decision (EU) 2020/2182

of 18 December 2020

laying down the final import response on behalf of the Union concerning the future import of certain chemicals pursuant to Regulation (EU) No 649/2012 of the European Parliament and of the Council and amending the Commission Implementing Decision of 15 May 2014 adopting Union import decisions for certain chemicals pursuant to that Regulation

(notified under document C(2020) 8977)

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EU) No 649/2012 of the European Parliament and of the Council of 4 July 2012 concerning the export and import of hazardous chemicals1, and in particular the second and third subparagraphs of Article 13(1) thereof,

After consulting the Committee established by Article 133 of Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC2,

Whereas:

(1)

The Rotterdam Convention on the Prior Informed Consent Procedure for Certain Hazardous Chemicals and Pesticides in International Trade ('the Convention') is implemented by Regulation (EU) No 649/2012. In accordance with that Regulation, the Commission is to provide the Secretariat of the Convention with final or interim import responses on behalf of the Union concerning the future import of all chemicals that are subject to the Prior Informed Consent procedure (the 'PIC procedure').

(2)

At its ninth meeting, held in Geneva from 29 April to 10 May 2019, the Conference of the Parties to the Convention agreed to list certain chemicals in Annex III to the Convention with the effect that they became subject to the PIC procedure. A decision guidance document for each chemical was sent to the Commission on 16 September 2019 with a request for a decision regarding future import of the chemical.

(3)

Phorate has been added to Annex III to the Convention as a pesticide. The placing on the market and use of phorate as a component of plant protection products is prohibited under Regulation (EC) No 1107/2009 of the European Parliament and of the Council3. Furthermore, the placing on the market and use of phorate as a component of biocidal products is prohibited under Regulation (EU) No 528/2012 of the European Parliament and of the Council4. Therefore, consent under the Rotterdam Convention should not be given to the future import of phorate to the Union.

(4)

Hexabromocyclododecane has been added to Annex III to the Convention as an industrial chemical. The manufacturing, placing on the market and use of hexabromocyclododecane are prohibited under Regulation (EU) 2019/1021 of the European Parliament and of the Council5. Therefore, consent under the Rotterdam Convention should not be given to the future import of hexabromocyclododecane to the Union.

(5)

Commercial pentabromodiphenyl ether (including tetra- and pentabromodiphenyl ether), commercial octabromodiphenyl ether (including hexa- and heptabromodiphenyl ether) and perfluorooctane sulfonic acid, perfluorooctane sulfonates, perfluorooctane sulfonamides and perfluorooctane sulfonyls were added to the PIC procedure as industrial chemicals at the sixth meeting of the Conference of the Parties to the Convention. Import responses for those chemicals have been adopted in the Commission Implementing Decision of 15 May 2014 adopting Union import decisions for certain chemicals pursuant to Regulation (EU) No 649/2012 of the European Parliament and of the Council6.

(6)

The manufacturing, placing on the market and use of commercial pentabromodiphenyl ether (including tetra- and pentabromodiphenyl ether) and commercial octabromodiphenyl ether (including hexa- and heptabromodiphenyl ether) are, subject to certain exemptions, prohibited under Regulation (EU) 2019/1021. Therefore, consent under the Rotterdam Convention should only be given to the future import of pentabromodiphenyl ether and commercial octabromodiphenyl ether to the Union, if certain conditions are met.

(7)

The manufacturing, placing on the market and use of perfluorooctane sulfonic acid, perfluorooctane sulfonates, perfluorooctane sulfonamides and perfluorooctane sulfonyls (PFOS) are, subject to certain exemptions, prohibited under Regulation (EU) 2019/1021. Therefore, consent under the Rotterdam Convention should only be given to the future import of PFOS to the Union, if certain conditions are met.

(8)

Since the regulatory developments in the Union brought about by Regulation (EU) 2019/1021 have taken place after the adoption of the Implementing Decision of 15 May 2014, that Decision should be amended accordingly,

HAS DECIDED AS FOLLOWS:

Article 1

The import responses for phorate and hexabromocyclododecane are set out in Annex I.

Article 2

Annex II to the Implementing Decision of 15 May 2014 adopting Union import decisions for certain chemicals pursuant to Regulation (EU) No 649/2012 is replaced by Annex II to this Decision.

Done at Brussels, 18 December 2020.

For the Commission

Virginijus Sinkevičius

Member of the Commission

ANNEX I

Import response for phorate

Image_r00001

FORM FOR IMPORT RESPONSE

Country:

European Union
Member States: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.
United Kingdom - The United Kingdom withdrew from the European Union as of 1 February 2020. During the transition period, which ends on 31 December 2020, unless extended, Union law, with a few limited exceptions, continues to be applicable to and in the United Kingdom and any reference to Member States in Union law shall be understood as including the United Kingdom.

SECTION 1IDENTITY OF CHEMICAL

1.1	Common name	Phorate
1.2	CAS number	298-02-2
1.3	Category	☒ Pesticide ☐ Industrial ☐ Severely hazardous pesticide formulation

SECTION 2INDICATION REGARDING PREVIOUS RESPONSE, IF ANY

2.1

☒

This is a first time import response for this chemical in the country.

2.2

☐

This is a modification of a previous response.

Date of issue of the previous response: …

SECTION 3RESPONSE REGARDING FUTURE IMPORT

☒

Final decision (Fill in section 4 below)

☐

Interim response (Fill in section 5 below)

SECTION 4FINAL DECISION, PURSUANT TO NATIONAL LEGISLATIVE OR ADMINISTRATIVE MEASURES

4.1	☒	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☒ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☒ Yes	☐ No
4.2	☐	Consent to import
4.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
4.4		National legislative or administrative measure upon which the final decision is based
		Description of the national legislative or administrative measure:
		In the Union, it is prohibited to place on the market or use plant protection products containing phorate, since that active substance has not been approved under Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC (OJ L 309, 24.11.2009, p. 1). Furthermore, it is prohibited to make available on the market or use biocidal products containing phorate, since that active substance has not been approved pursuant to 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 (OJ L167, 27.6.2012, p.1).

SECTION 5INTERIM RESPONSE

5.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
5.2	☐	Consent to import
5.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
5.4		Indication of active consideration in order to reach a final decision
		Is a final decision under active consideration?	☐ Yes	☐ No
5.5		Information or assistance requested in order to reach a final decision
		The following additional information is requested from the Secretariat:

		The following additional information is requested from the country that notified the final regulatory action:

		The following assistance is requested from the Secretariat in evaluating the chemical:

SECTION 6RELEVANT ADDITIONAL INFORMATION, WHICH MAY INCLUDE:

Is this chemical currently registered in the country?	☐ Yes	☒ No
Is this chemical manufactured in the country?	☐ Yes	☒ No
If yes to either one of these questions:
Is this intended for domestic use?	☐ Yes	☐ No
Is this intended for export?	☐ Yes	☐ No

Other remarks

In accordance with Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006 (OJ L 353, 31.12.2008, p.1), which implements the UN Globally Harmonised System of Classification and Labelling of Chemicals in the Union, phorate is classified as:

Acute Toxicity 2* - H300 – Fatal if swallowed.

Acute Toxicity 1 – H310 – Fatal in contact with skin.

Aquatic Acute 1 – H 400 - Very toxic to aquatic life.

Aquatic Chronic 1 - H410 - Very toxic to aquatic life with long lasting effects.

(* = This classification is to be considered as a minimum classification)

SECTION 7DESIGNATED NATIONAL AUTHORITY

Institution	European Commission, DG Environment
Address	Rue de la Loi 200, B-1049 Brussels, Belgium
Name of person in charge	Dr. Juergen Helbig
Position of person in charge	International Chemicals Policy Coordinator
Telephone	32 2 298 85 21
Telefax	32 2 296 76 16
E-mail address	Juergen.Helbig@ec.europa.eu

Date, signature of DNA and official seal: ___________________________________

PLEASE RETURN THE COMPLETED FORM TO:

Secretariat for the Rotterdam Convention

Food and Agriculture Organization

of the United Nations (FAO)

Viale delle Terme di Caracalla

I - 00100 Rome, Italy

Tel: (+39 06) 5705 3441

Fax: (+39 06) 5705 6347

E-mail: pic@pic.int

Secretariat for the Rotterdam Convention

United Nations Environment

Programme (UNEP)

11-13, Chemin des Anémones

CH - 1219 Châtelaine, Geneva, Switzerland

Tel: (+41 22) 917 8177

Fax: (+41 22) 917 8082

E-mail: pic@pic.int

Import response for hexabromocyclododecane

Image_r00002

FORM FOR IMPORT RESPONSE

Country:

European Union
Member States: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.
United Kingdom - The United Kingdom withdrew from the European Union as of 1 February 2020. During the transition period, which ends on 31 December 2020, unless extended, Union law, with a few limited exceptions, continues to be applicable to and in the United Kingdom and any reference to Member States in Union law shall be understood as including the United Kingdom.

SECTION 1I DENTITY OF CHEMICAL

1.1	Common name	Hexabromocyclododecane
1.2	CAS number	134237-50-6, 134237-51-7, 134237-52-8, 25637-99-4, 3194-55-6
1.3	Category	☐ Pesticide ☒ Industrial ☐ Severely hazardous pesticide formulation

SECTION 2INDICATION REGARDING PREVIOUS RESPONSE, IF ANY

2.1

☒

This is a first time import response for this chemical in the country.

2.2

☐

This is a modification of a previous response.

Date of issue of the previous response: …

SECTION 3RESPONSE REGARDING FUTURE IMPORT

☒

Final decision (Fill in section 4 below)

☐

Interim response (Fill in section 5 below)

SECTION 4FINAL DECISION, PURSUANT TO NATIONAL LEGISLATIVE OR ADMINISTRATIVE MEASURES

4.1	☒	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☒ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☒ Yes	☐ No
4.2	☐	Consent to import
4.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
4.4		National legislative or administrative measure upon which the final decision is based
		Description of the national legislative or administrative measure:
		In the Union, the manufacturing, placing on the market and use of hexabromocyclododecane are prohibited under Regulation (EU) 2019/1021 of the European Parliament and of the Council on persistent organic pollutants (OJ L 169, 25.6.2019, p. 45).

SECTION 5INTERIM RESPONSE

5.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
5.2	☐	Consent to import
5.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
5.4		Indication of active consideration in order to reach a final decision
		Is a final decision under active consideration?	☐ Yes	☐ No
5.5		Information or assistance requested in order to reach a final decision
		The following additional information is requested from the Secretariat:

		The following additional information is requested from the country that notified the final regulatory action:

		The following assistance is requested from the Secretariat in evaluating the chemical:

SECTION 6RELEVANT ADDITIONAL INFORMATION, WHICH MAY INCLUDE:

Is this chemical currently registered in the country?	☐ Yes	☒ No
Is this chemical manufactured in the country?	☐ Yes	☒ No
If yes to either one of these questions:
Is this intended for domestic use?	☐ Yes	☐ No
Is this intended for export?	☐ Yes	☐ No

Other remarks

Repro. 2 – H361 - Suspected of damaging fertility or the unborn child.

Lact. – H362 - May cause harm to breast-fed children.

SECTION 7DESIGNATED NATIONAL AUTHORITY

Institution	European Commission, DG Environment
Address	Rue de la Loi 200, B-1049 Brussels, Belgium
Name of person in charge	Dr. Juergen Helbig
Position of person in charge	International Chemicals Policy Coordinator
Telephone	32 2 298 85 21
Telefax	32 2 296 76 16
E-mail address	Juergen.Helbig@ec.europa.eu

Date, signature of DNA and official seal: ___________________________________

PLEASE RETURN THE COMPLETED FORM TO:

Secretariat for the Rotterdam Convention

Food and Agriculture Organization

of the United Nations (FAO)

Viale delle Terme di Caracalla

I - 00100 Rome, Italy

Tel: (+39 06) 5705 3441

Fax: (+39 06) 5705 6347

E-mail: pic@pic.int

Secretariat for the Rotterdam Convention

United Nations Environment

Programme (UNEP)

11-13, Chemin des Anémones

CH - 1219 Châtelaine, Geneva, Switzerland

Tel: (+41 22) 917 8177

Fax: (+41 22) 917 8082

E-mail: pic@pic.int

ANNEX II

Import response for commercial pentabromodiphenyl ether

Image_r00003

FORM FOR IMPORT RESPONSE

Country:

European Union
Member States: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.
United Kingdom - The United Kingdom withdrew from the European Union as of 1 February 2020. During the transition period, which ends on 31 December 2020, unless extended, Union law, with a few limited exceptions, continues to be applicable to and in the United Kingdom and any reference to Member States in Union law shall be understood as including the United Kingdom.

SECTION 1IDENTITY OF CHEMICAL

1.1

Common name

Commercial pentabromodiphenyl ether including:

Tetrabromodiphenyl ether

- Pentabromodiphenyl ether

1.2

CAS number

40088-47-9 - Tetrabromodiphenyl ether

32534-81-9 - Pentabromodiphenyl ether

1.3

SECTION 2INDICATION REGARDING PREVIOUS RESPONSE, IF ANY

2.1

☐

This is a first time import response for this chemical in the country.

2.2

☒

This is a modification of a previous response.

Date of issue of the previous response: …18 June 2014…

SECTION 3RESPONSE REGARDING FUTURE IMPORT

☒

Final decision (Fill in section 4 below)

☐

Interim response (Fill in section 5 below)

SECTION 4FINAL DECISION, PURSUANT TO NATIONAL LEGISLATIVE OR ADMINISTRATIVE MEASURES

4.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☒ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☒ Yes	☐ No
4.2	☐	Consent to import
4.3	☒	Consent to import only subject to specified conditions
		The specified conditions are:
		Pursuant to Regulation (EU) 2019/1021, the placing on the market and use of commercial pentabromodiphenyl ether is only allowed in accordance with Directive 2011/65/EU, where the following provisions apply: The import of commercial pentabromodiphenyl ether is only allowed for placing on the market and use in cables or spare parts for the repair, the reuse, the updating of functionalities or upgrading of capacity of the following: (a) electrical and electronic equipment (EEE) placed on the market before 1 July 2006; (b) medical devices placed on the market before 22 July 2014; (c) in vitro diagnostic medical devices placed on the market before 22 July 2016; (d) monitoring and control instruments placed on the market before 22 July 2014; (e) industrial monitoring and control instruments placed on the market before 22 July 2017; (f) all other EEE that was outside the scope of Directive 2002/95/EC and which is placed on the market before 22 July 2019; (g) EEE which benefited from an exemption and which was placed on the market before that exemption expired as far as that specific exemption is concerned. Spare parts are defined as a separate part of an EEE that can replace a part of an EEE. The EEE cannot function as intended without that part of the EEE. The functionality of EEE is restored or is upgraded when the part is replaced by a spare part.
		Are the conditions for import of the chemical the same for all sources of import?	☒ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☒ Yes	☐ No
4.4		National legislative or administrative measure upon which the final decision is based
		Description of the national legislative or administrative measure:
		In the Union, the manufacturing, placing on the market and use of tetrabromodiphenyl ether and pentabromodiphenyl ether are, subject to certain exemptions, prohibited pursuant to Regulation (EU) 2019/1021 of the European Parliament and of the Council of 20 June 2019 on persistent organic pollutants (OJ L 169, 25.06.2019, p. 45).

SECTION 5INTERIM RESPONSE

5.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
5.2	☐	Consent to import
5.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
5.4		Indication of active consideration in order to reach a final decision
		Is a final decision under active consideration?	☐ Yes	☐ No
5.5		Information or assistance requested in order to reach a final decision
		The following additional information is requested from the Secretariat:

		The following additional information is requested from the country that notified the final regulatory action:

		The following assistance is requested from the Secretariat in evaluating the chemical:

SECTION 6RELEVANT ADDITIONAL INFORMATION, WHICH MAY INCLUDE:

Is this chemical currently registered in the country?	☐ Yes	☒ No
Is this chemical manufactured in the country?	☐ Yes	☒ No
If yes to either one of these questions:
Is this intended for domestic use?	☐ Yes	☐ No
Is this intended for export?	☐ Yes	☐ No

Other remarks

Lact. – H 362 – May cause harm to breast-fed children.

STOT RE 2 * – H 373 - May cause damage to organs through prolonged or repeated exposure.

Aquatic Acute 1 – H 400 - Very toxic to aquatic life.

Aquatic Chronic 1 – H 410 - Very toxic to aquatic life with long lasting effects.

(* = This classification is to be considered as a minimum classification)

SECTION 7DESIGNATED NATIONAL AUTHORITY

Institution	European Commission, DG Environment
Address	Rue de la Loi 200, B-1049 Brussels, Belgium
Name of person in charge	Dr. Juergen Helbig
Position of person in charge	International Chemicals Policy Coordinator
Telephone	32 2 298 85 21
Telefax	32 2 296 76 16
E-mail address	Juergen.Helbig@ec.europa.eu

Date, signature of DNA and official seal: ___________________________________

PLEASE RETURN THE COMPLETED FORM TO:

Secretariat for the Rotterdam Convention

Food and Agriculture Organization

of the United Nations (FAO)

Viale delle Terme di Caracalla

I - 00100 Rome, Italy

Tel: (+39 06) 5705 3441

Fax: (+39 06) 5705 6347

E-mail: pic@pic.int

Secretariat for the Rotterdam Convention

United Nations Environment

Programme (UNEP)

11-13, Chemin des Anémones

CH - 1219 Châtelaine, Geneva, Switzerland

Tel: (+41 22) 917 8177

Fax: (+41 22) 917 8082

E-mail: pic@pic.int

Import response for commercial octabromodiphenyl ether

Image_r00004

FORM FOR IMPORT RESPONSE

Country:

European Union
Member States: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.
United Kingdom - The United Kingdom withdrew from the European Union as of 1 February 2020. During the transition period, which ends on 31 December 2020, unless extended, Union law, with a few limited exceptions, continues to be applicable to and in the United Kingdom and any reference to Member States in Union law shall be understood as including the United Kingdom.

SECTION 1IDENTITY OF CHEMICAL

1.1

Common name

Commercial octabromodiphenyl ether including:

Hexabromodiphenyl ether
Heptabromodiphenyl ether

1.2

CAS number

36483-60-0 - Hexabromodiphenyl ether

68928-80-3 - Heptabromodiphenyl ether

1.3

SECTION 2INDICATION REGARDING PREVIOUS RESPONSE, IF ANY

2.1

☐

This is a first time import response for this chemical in the country.

2.2

☒

This is a modification of a previous response.

Date of issue of the previous response: …18 June 2014…

SECTION 3RESPONSE REGARDING FUTURE IMPORT

☒

Final decision (Fill in section 4 below)

☐

Interim response (Fill in section 5 below)

SECTION 4FINAL DECISION, PURSUANT TO NATIONAL LEGISLATIVE OR ADMINISTRATIVE MEASURES

4.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
4.2	☐	Consent to import
4.3	☒	Consent to import only subject to specified conditions
		The specified conditions are:
		Pursuant to Regulation (EU) 2019/1021, the placing on the market and use of commercial octabromodiphenyl ether is only allowed in accordance with Directive 2011/65/EU, where the following provisions apply: The import of commercial octabromodiphenyl ether is only allowed for placing on the market and use in cables or spare parts for the repair, the reuse, the updating of functionalities or upgrading of capacity of the following: (a) electrical and electronic equipment (EEE) placed on the market before 1 July 2006; (b) medical devices placed on the market before 22 July 2014; (c) in vitro diagnostic medical devices placed on the market before 22 July 2016; (d) monitoring and control instruments placed on the market before 22 July 2014; (e) industrial monitoring and control instruments placed on the market before 22 July 2017; (f) all other EEE that was outside the scope of Directive 2002/95/EC and which is placed on the market before 22 July 2019; (g) EEE which benefited from an exemption and which was placed on the market before that exemption expired as far as that specific exemption is concerned. Spare parts are defined as a separate part of an EEE that can replace a part of an EEE. The EEE cannot function as intended without that part of the EEE. The functionality of EEE is restored or is upgraded when the part is replaced by a spare part.
		Are the conditions for import of the chemical the same for all sources of import?	☒ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☒ Yes	☐ No
4.4		National legislative or administrative measure upon which the final decision is based
		Description of the national legislative or administrative measure:
		In the Union, the manufacturing, placing on the market and use of hexabromodiphenyl ether and heptabromodiphenyl ether are prohibited pursuant to Regulation (EU) 2019/1021 of the European Parliament and of the Council of 20 June 2019 on persistent organic pollutants (OJ L 169, 25.06.2019, p. 45).

SECTION 5INTERIM RESPONSE

5.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
5.2	☐	Consent to import
5.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
5.4		Indication of active consideration in order to reach a final decision
		Is a final decision under active consideration?	☐ Yes	☐ No
5.5		Information or assistance requested in order to reach a final decision
		The following additional information is requested from the Secretariat:

		The following additional information is requested from the country that notified the final regulatory action:

		The following assistance is requested from the Secretariat in evaluating the chemical:

SECTION 6RELEVANT ADDITIONAL INFORMATION, WHICH MAY INCLUDE:

Is this chemical currently registered in the country?	☐ Yes	☒ No
Is this chemical manufactured in the country?	☐ Yes	☒ No
If yes to either one of these questions:
Is this intended for domestic use?	☐ Yes	☐ No
Is this intended for export?	☐ Yes	☐ No

Other remarks

SECTION 7DESIGNATED NATIONAL AUTHORITY

Institution	European Commission, DG Environment
Address	Rue de la Loi 200, B-1049 Brussels, Belgium
Name of person in charge	Dr. Juergen Helbig
Position of person in charge	International Chemicals Policy Coordinator
Telephone	32 2 298 85 21
Telefax	32 2 296 76 16
E-mail address	Juergen.Helbig@ec.europa.eu

Date, signature of DNA and official seal: ___________________________________

PLEASE RETURN THE COMPLETED FORM TO:

Secretariat for the Rotterdam Convention

Food and Agriculture Organization

of the United Nations (FAO)

Viale delle Terme di Caracalla

I - 00100 Rome, Italy

Tel: (+39 06) 5705 3441

Fax: (+39 06) 5705 6347

E-mail: pic@pic.int

Secretariat for the Rotterdam Convention

United Nations Environment

Programme (UNEP)

11-13, Chemin des Anémones

CH - 1219 Châtelaine, Geneva, Switzerland

Tel: (+41 22) 917 8177

Fax: (+41 22) 917 8082

E-mail: pic@pic.int

Import response for perfluorooctane sulfonic acid, perfluorooctane sulfonates, perfluorooctane sulfonamides and perfluorooctane sulfonyls

Image_r00005

FORM FOR IMPORT RESPONSE

Country:

European Union
Member States: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.
United Kingdom - The United Kingdom withdrew from the European Union as of 1 February 2020. During the transition period, which ends on 31 December 2020, unless extended, Union law, with a few limited exceptions, continues to be applicable to and in the United Kingdom and any reference to Member States in Union law shall be understood as including the United Kingdom.

SECTION 1IDENTITY OF CHEMICAL

1.1

Common name

Perfluorooctane sulfonic acid, perfluorooctane sulfonates, perfluorooctane sulfonamides and perfluorooctane sulfonyls

1.2

CAS number

Relevant CAS numbers are:

1763-23-1 - Perfluorooctane sulfonic acid

2795-39-3 - Potassium perfluorooctane sulfonate

29457-72-5 - Lithium perfluorooctane sulfonate

29081-56-9 - Ammonium perfluorooctane sulfonate

70225-14-8 - Diethanolamine perfluorooctane sulfonate

56773-42-3 - Tetraethylammonium perfluorooctane sulfonate

251099-16-8 - Didecyldimethylammonium perfluorooctane sulfonate

4151-50-2 - N-Ethylperfluorooctane sulfonamide

31506-32-8 - N-Methylperfluorooctane sulfonamide

1691-99-2 - N-Ethyl-N-(2-hydroxyethyl) perfluorooctane sulfonamide

24448-09-7 - N-(2-hydroxyethyl)-N-methylperfluorooctane sulfonamide

307-35-7 - Perfluorooctane sulfonyl fluoride

1.3

SECTION 2INDICATION REGARDING PREVIOUS RESPONSE, IF ANY

2.1

☐

This is a first time import response for this chemical in the country.

2.2

☒

This is a modification of a previous response.

Date of issue of the previous response: …18 June 2014 …

SECTION 3RESPONSE REGARDING FUTURE IMPORT

☒

Final decision (Fill in section 4 below)

☐

Interim response (Fill in section 5 below)

SECTION 4FINAL DECISION, PURSUANT TO NATIONAL LEGISLATIVE OR ADMINISTRATIVE MEASURES

4.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
4.2	☐	Consent to import
4.3	☒	Consent to import only subject to specified conditions
		The specified conditions are:
		Imports of perfluorooctane sulfonic acid and its derivatives (PFOS) must be in compliance with Regulation (EU) 2019/1021 of the European Parliament and of the Council of 20 June 2019 on persistent organic pollutants (OJ L 169, 25.06.2019, p. 45), which sets out the following: 1. The production, placing on the market and use of PFOS, whether on their own, in mixtures or as constituents of articles, shall be prohibited. 2. The prohibition shall not apply to PFOS occurring as an unintentional trace contaminant in substances, mixtures or articles, provided that (a) concentrations of PFOS are equal to or below 10 mg/kg (0,001 % by weight) when it occurs in substances or in mixtures or (b) concentrations of PFOS in semi-finished products or articles, or parts thereof, are lower than 0,1 % by weight calculated with reference to the mass of structurally or micro-structurally distinct parts that contain PFOS or, for textiles or other coated materials, if the amount of PFOS is lower than 1 μg/m 2 of the coated material. 3. If the quantity of PFOS released into the environment is minimised, production and placing on the market is allowed for the following specific uses provided that Member States report to the Commission every four years on progress made to eliminate PFOS: mist suppressants for non-decorative hard chromium (VI) plating in closed loop systems.
		Are the conditions for import of the chemical the same for all sources of import?	☒ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☒ Yes	☐ No
4.4		National legislative or administrative measure upon which the final decision is based
		Description of the national legislative or administrative measure:
		In the Union, the manufacturing, placing on the market and use of perfluorooctane sulfonic acid and its derivatives (PFOS) are prohibited pursuant to Regulation (EU) 2019/1021 of the European Parliament and of the Council of 20 June 2019 on persistent organic pollutants (OJ L 169, 25.06.2019, p. 45). However, that Regulation allows for specific exemptions, which are outlined in section 4.3.

SECTION 5NTERIM RESPONSE

5.1	☐	No consent to import
		Is the import of the chemical from all sources simultaneously prohibited?	☐ Yes	☐ No
		Is domestic production of the chemical for domestic use simultaneously prohibited?	☐ Yes	☐ No
5.2	☐	Consent to import
5.3	☐	Consent to import only subject to specified conditions
		The specified conditions are:

		Are the conditions for import of the chemical the same for all sources of import?	☐ Yes	☐ No
		Are the conditions for domestic production of the chemical for domestic use the same as for all imports?	☐ Yes	☐ No
5.4		Indication of active consideration in order to reach a final decision
		Is a final decision under active consideration?	☐ Yes	☐ No
5.5		Information or assistance requested in order to reach a final decision
		The following additional information is requested from the Secretariat:

		The following additional information is requested from the country that notified the final regulatory action:

		The following assistance is requested from the Secretariat in evaluating the chemical:

SECTION 6RELEVANT ADDITIONAL INFORMATION, WHICH MAY INCLUDE:

Is this chemical currently registered in the country?	☒ Yes	☐ No
Is this chemical manufactured in the country?	☒ Yes	☐ No
If yes to either one of these questions:
Is this intended for domestic use?	☒ Yes	☐ No
Is this intended for export?	☒ Yes	☐ No

Other remarks

Acute Tox. 4 * - H302 - Harmful if swallowed.

Acute Tox. 4 * - H332 – Harmful if inhaled.

Carc. 2 - H351 – Suspected of causing cancer.

Lact. - H362 – May cause harm to breast-fed children.

STOT RE 1 - H372 - Causes damage to organs through prolonged or repeated exposure.

Aquatic Chronic 2 - H411 - Toxic to aquatic life with long lasting effects.

Repr. 1B - H360D - May damage the unborn child.

(* = This classification is to be considered as a minimum classification)

SECTION 7DESIGNATED NATIONAL AUTHORITY

Institution	European Commission, DG Environment
Address	Rue de la Loi 200, B-1049 Brussels, Belgium
Name of person in charge	Dr. Juergen Helbig
Position of person in charge	International Chemicals Policy Coordinator
Telephone	32 2 298 85 21
Telefax	32 2 296 76 16
E-mail address	Juergen.Helbig@ec.europa.eu

Date, signature of DNA and official seal: ___________________________________

PLEASE RETURN THE COMPLETED FORM TO:

Secretariat for the Rotterdam Convention

Food and Agriculture Organization

of the United Nations (FAO)

Viale delle Terme di Caracalla

I - 00100 Rome, Italy

Tel: (+39 06) 5705 3441

Fax: (+39 06) 5705 6347

E-mail: pic@pic.int

Secretariat for the Rotterdam Convention

United Nations Environment

Programme (UNEP)

11-13, Chemin des Anémones

CH - 1219 Châtelaine, Geneva, Switzerland

Tel: (+41 22) 917 8177

Fax: (+41 22) 917 8082

E-mail: pic@pic.int