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Document 32021R1044

    Commission Implementing Regulation (EU) 2021/1044 of 22 June 2021 granting a Union authorisation for the single biocidal product ‘Pesguard® Gel’ (Text with EEA relevance)

    C/2021/4442

    OJ L 225, 25.6.2021, p. 54–61 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    Legal status of the document In force: This act has been changed. Current consolidated version: 29/12/2022

    ELI: http://data.europa.eu/eli/reg_impl/2021/1044/oj

    25.6.2021   

    EN

    Official Journal of the European Union

    L 225/54


    COMMISSION IMPLEMENTING REGULATION (EU) 2021/1044

    of 22 June 2021

    granting a Union authorisation for the single biocidal product ‘Pesguard® Gel’

    (Text with EEA relevance)

    THE EUROPEAN COMMISSION,

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

    Having regard 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 (1), and in particular the first subparagraph of Article 44(5) thereof,

    Whereas:

    (1)

    On 21 September 2016, Sumitomo Chemical Agro Europe SAS submitted an application in accordance with Article 43(1) of Regulation (EU) No 528/2012 for authorisation of a single biocidal product named ‘Pesguard® Gel’ of product-type 18, as described in Annex V to that Regulation, providing written confirmation that the competent authority of the Netherlands had agreed to evaluate the application. The application was recorded under case number BC-HS027052-37 in the Register for Biocidal Products.

    (2)

    ‘Pesguard® Gel’ contains pyriproxyfen and clothianidin, as the active substances, which are included in the Union list of approved active substances referred to in Article 9(2) of Regulation (EU) No 528/2012.

    (3)

    On 31 March 2020, the evaluating competent authority submitted, in accordance with Article 44(1) of Regulation (EU) No 528/2012, an assessment report and the conclusions of its evaluation to the European Chemicals Agency (‘the Agency’).

    (4)

    On 13 October 2020, the Agency submitted to the Commission an opinion (2), the draft summary of the biocidal product characteristics (‘SPC’) of ‘Pesguard® Gel’ and the final assessment report on the single biocidal product in accordance with Article 44(3) of Regulation (EU) No 528/2012.

    (5)

    The opinion concludes that ‘Pesguard® Gel’ is a biocidal product, that it is eligible for Union authorisation in accordance with Article 42(1) of Regulation (EU) No 528/2012 and that subject to compliance with the draft SPC, it meets the conditions laid down in Article 19(1) of that Regulation.

    (6)

    On 26 October 2020, the Agency transmitted to the Commission the draft SPC in all the official languages of the Union in accordance with Article 44(4) of Regulation (EU) No 528/2012.

    (7)

    The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for ‘Pesguard® Gel’.

    (8)

    According to the opinion of the Agency, as regards the non-active substances cis CTAC and dichloromethane contained in ‘Pesguard® Gel’, it was not possible to conclude whether they meet the scientific criteria for the determination of endocrine-disrupting properties set out in Commission Delegated Regulation (EU) 2017/2100 (3) within the period for the evaluation of the application. Further examination of cis CTAC and dichloromethane should therefore take place. If it is concluded that either cis CTAC or dichloromethane or both are considered as having endocrine-disrupting properties, the Commission will consider whether to cancel or amend the Union authorisation for ‘Pesguard® Gel’ in accordance with Article 48 of Regulation (EU) No 528/2012.

    (9)

    The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Biocidal Products,

    HAS ADOPTED THIS REGULATION:

    Article 1

    A Union authorisation with authorisation number EU-0024951-0000 is granted to Sumitomo Chemical Agro Europe SAS for the making available on the market and use of the single biocidal product ‘Pesguard® Gel’ in accordance with the summary of the biocidal product characteristics set out in the Annex.

    The Union authorisation is valid from 15 July 2021 until 30 June 2031.

    Article 2

    This Regulation shall enter into force on the twentieth day following that of 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, 22 June 2021.

    For the Commission

    The President

    Ursula VON DER LEYEN


    (1)   OJ L 167, 27.6.2012, p. 1.

    (2)  ECHA opinion of 8 October 2020 on the Union authorisation of the biocidal product ‘Pesguard® Gel’ (ECHA/BPC/269/2020), https://echa.europa.eu/it/opinions-on-union-authorisation

    (3)  Commission Delegated Regulation (EU) 2017/2100 of 4 September 2017 setting out scientific criteria for the determination of endocrine-disrupting properties pursuant to Regulation (EU) No 528/2012 of the European Parliament and Council (OJ L 301, 17.11.2017, p. 1).


    ANNEX

    Summary of product characteristics for a biocidal product

    Pesguard® Gel

    Product type 18 – Insecticides, acaricides and products to control other arthropods (Pest control)

    Authorisation number: EU-0024951-0000

    R4BP asset number: EU-0024951-0000

    1.   ADMINISTRATIVE INFORMATION

    1.1.   Trade name(s) of the product

    Trade name(s)

    Pesguard® Gel

    1.2.   Authorisation holder

    Name and address of the authorisation holder

    Name

    Sumitomo Chemical Agro Europe SAS

    Address

    Parc d’Affaires de Crécy 10A, rue de la Voie Lactée, 69370 Saint Didier au Mont d’Or, France

    Authorisation number

    EU-0024951-0000

    R4BP asset number

    EU-0024951-0000

    Date of the authorisation

    15 July 2021

    Expiry date of the authorisation

    30 June 2031

    1.3.   Manufacturer(s) of the product

    Name of manufacturer

    McLaughlin Gormley King Company (MGK)

    Address of manufacturer

    8810 10th Avenue North, MN 55427 Minneapolis United States

    Location of manufacturing sites

    McLaughlin Gormley King Company, 4001 Peavey Road, MN 55318 Chaska United States

    1.4.   Manufacturer(s) of the active substance(s)

    Active substance

    (E)-1-(2-Chloro-1,3-thiazol-5-ylmethyl)-3- methyl-2-nitroguanidine (Clothianidin)

    Name of manufacturer

    Sumitomo Chemical Co. Ltd

    Address of manufacturer

    27-1, Shinkawa 2-chome, Chuo-ku, 104-8260 Tokyo Japan

    Location of manufacturing sites

    Sumitomo Chemical Company LTD, Oita Works, 2200, Tsurusaki, Oita City„ 870-0106 Oita Japan


    Active substance

    pyriproxyfen

    Name of manufacturer

    Sumitomo Chemical Co. Ltd

    Address of manufacturer

    27-1, Shinkawa 2-chome, Chuo-ku, 104-8260 Tokyo Japan

    Location of manufacturing sites

    Sumitomo Chemical Company LTD, Misawa Works, Aza-Sabishirotaira, Oaza-Misawa, Misawa„ 033-0022 Aomori Japan

    2.   PRODUCT COMPOSITION AND FORMULATION

    2.1.   Qualitative and quantitative information on the composition of the product

    Common name

    IUPAC name

    Function

    CAS number

    EC number

    Content (%)

    Clothianidin

    (E)-1-(2-Chloro-1,3-thiazol-5-ylmethyl)-3- methyl-2-nitroguanidine

    Active Substance

    210880-92-5

    433-460-1

    0,526

    pyriproxyfen

    4-phenoxyphenyl (RS)-2-(2- pyridyloxy)propyl ether

    Active Substance

    95737-68-1

    429-800-1

    0,515

    Acetic acid

    Ethanoic acid

    Non-active substance

    64-19-7

    200-580-7

    0,3

    Potassium sorbate

    potassium (E,E)-hexa-2,4-dienoate

    Non-active substance

    24634-61-5

    246-376-1

    0,5

    2.2.   Type of formulation

    RB – Bait (ready for use)

    3.   HAZARD AND PRECAUTIONARY STATEMENTS

    Hazard statements

    May cause an allergic skin reaction.

    Very toxic to aquatic life with long lasting effects.

    Precautionary statements

    IF ON SKIN:Wash with plenty of water.

    If skin irritation or rash occurs: Get medical advice.

    Wear protective gloves.

    Avoid release to the environment.

    Dispose of container in accordance with local regulations.

    Collect spillage.

    4.   AUTHORISED USE(S)

    4.1.   Use description

    Table 1. Use # 1 – Professional Use – RTU Bait

    Product type

    PT18 – Insecticides, acaricides and products to control other arthropods (Pest control)

    Where relevant, an exact description of the authorised use

    Insecticide

    Target organism(s) (including development stage)

    Scientific name: Blattella germanica

    Common name: German cockroach

    Development stage: Nymphs

    Scientific name: Blattella germanica

    Common name: German cockroach

    Development stage: Adults

    Scientific name: Supella longipalpa

    Common name: Brown-banded cockroach

    Development stage: Nymphs

    Scientific name: Supella longipalpa

    Common name: Brown-banded cockroach

    Development stage: Adults

    Scientific name: Blatta orientalis

    Common name: Oriental Cockroach

    Development stage: Nymphs

    Scientific name: Blatta orientalis

    Common name: Oriental Cockroach

    Development stage: Adults

    Scientific name: Periplaneta americana

    Common name: American Cockroach

    Development stage: Nymphs

    Scientific name: Periplaneta americana

    Common name: American Cockroach

    Development stage: Adults

    Field(s) of use

    Indoor

    In cracks and crevices, or in concealed locations inaccessible to humans or domestic animals: behind refrigerators cupboards and shelves, under kitchen appliances, in electrical control boxes, voids and ducting and under bathroom fixtures etc.

    Application method(s)

    Bait application

    A ready to use (RTU) insecticidal gel bait for the control of cockroaches in public hygiene

    Application rate(s) and frequency

    Pesguard® Gel should be applied as a number of spots of approximately 4 mm diameter (each spot comprising approximately 0,032 g of bait).

    In cases of severe infestation, where larger cockroach species are present (B. orientalis or P. americana), in areas that are particularly dirty or cluttered or where alternative sources of food cannot be entirely eliminated the higher application rate (e.g. 2 instead of 1 spot per m2 in case of a light infestation) should be used.

    Light infestation 1 – 2 (0,032 – 0,064 g) spots per m2

    Medium infestation 3 – 6 (0,096 – 0,192 g) spots per m2

    Heavy infestation 6 – 10 (0,192 – 0,320 g) spots per m2

    The maximum number of annual applications is 11.

    Category(ies) of users

    Professional

    Pack sizes and packaging material

    30 g Polypropylene (PP) syringe

    Screw top cap High Density Poly Ethylene (HDPE)

    4.1.1.   Use-specific instructions for use

    See the general directions for use.

    4.1.2.   Use-specific risk mitigation measures

    See the general directions for use.

    4.1.3.   Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment

    See the general directions for use.

    4.1.4.   Where specific to the use, the instructions for safe disposal of the product and its packaging

    See the general directions for use.

    4.1.5.   Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage

    See the general directions for use.

    5.   GENERAL DIRECTIONS FOR USE (1)

    5.1.   Instructions for use

    Always read the label or leaflet before use and respect/follow all the instructions provided.

    Do not expose bait drops to sunlight or heat (e.g. radiator).

    The pre-filled plastic reservoir containing Pesguard® Gel is intended for use with the plunger provided or a specific bait application device common to the pest control industry. Refer to the manufacturer’s instructions for directions on the use of the applicator.

    Inject the bait into cracks and crevices, void spaces, or in concealed locations inaccessible to humans or domestic animals where insects may live, feed and breed. Such areas are generally warm/damp and dark (behind refrigerators, cupboards and shelves, under kitchen appliances, in electrical control boxes, voids and ducting and under bathroom fixtures etc.). Inspection or trapping to confirm infestation is recommended prior to treatment. Ensure that any alternative food sources are removed and concentrate the bait placements as individual spots at cockroach activity sites. The product should not be applied to areas accessible to children and pets.

    Do not apply Pesguard® Gel where it will come into contact with water or in areas that are routinely cleaned. Typically cockroaches will die a few hours after a single feed on Pesguard® Gel. In infested premises, dead cockroaches will normally be seen within 24 hours of treatment.

    Remove the cap from the nozzle, touch the top to the surface to be treated, and push down on the plunger. Replace the cap on the dispenser after treatment is completed.

    The bait will adhere to non-greasy or non-dusty surfaces and will remain pliable and palatable to cockroaches as long as it is visibly present.

    Treated area’s should be visually inspected after 1-2 weeks. Where initial infestation was heavy a second Pesguard® Gel application may be required if the first treatment has been consumed and live cockroaches are still present.

    A second visual inspection of bait placements is recommended 2-4 weeks after the initial treatment. Reapply when bait is no longer visibly present, according to the level of infestation (light, medium or heavy). Replace bait before it is completely consumed to keep cockroaches from returning.

    Inform the registration holder if the treatment is ineffective.

    Spills and residues containing the product need to be removed as chemical waste.

    Care should be taken to avoid depositing gel onto exposed surfaces. If gel contacts an exposed surface, remove gel with a paper towel and clean the area with disposable wet wipes.

    During follow-up visits, inspect bait placements and re-apply when necessary.

    Do not place bait in locations that are routinely washed, as bait will be removed by washing. Do not use this product in or on electrical equipment where a possibility of shock hazard exists. Avoid contact with textiles and clothing, as bait may stain.

    5.2.   Risk mitigation measures

    Wear protective chemical resistant gloves during product handling phase (glove material to be specified by the authorisation holder within the product information).

    Do not apply bait in areas where repellent insecticides have been used without thoroughly cleaning the surface with disposable wet tissue. Do not apply repellent insecticides after application of the bait.

    Do not apply directly on or near food, feed or drinks, or on surfaces or utensils likely to be in direct contact with food, feed, drinks and animals.

    Spills and residues containing the product must be removed as chemical waste.

    Avoid placing gel on fabrics or carpets since it may stain some absorbent materials. To prevent staining, exposed bait should be cleaned up immediately with disposable wet wipes.

    Cleaning materials must be disposed of as to solid waste.

    5.3.   Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment

    This biocidal product contains clothianidin, which is dangerous to bees.

    Description of first aid measures

    Skin contact: Remove contaminated clothing immediately and wash skin with soap and water. Get medical attention if irritation persists after washing.

    Eye contact: If symptoms occur, rinse with water. Remove contact lenses, if present and easy to do. Call a POISON CENTRE or a doctor.

    Ingestion: If swallowed: If symptons occur call a POISON CENTRE or a doctor.

    If inhaled: not applicable.

    Most important symptoms and effects, both acute and delayed

    Eyes: May cause temporary eye irritation.

    Emergency measures to protect the environment

    Avoid release of the product to the environment.

    5.4.   Instructions for safe disposal of the product and its packaging

    Only pass on empty containers/packaging for recycling.

    Disposal of this packaging should at all times comply with the waste disposal legislation and any regional local authority requirements.

    5.5.   Conditions of storage and shelf-life of the product under normal conditions of storage

    Protect from frost. Store away from direct sunlight.

    Shelf life: 2 years.

    6.   OTHER INFORMATION


    (1)  Instructions for use, risk mitigation measures and other directions for use under this section are valid for any authorised uses.


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