INHALT

Commission Implementing Regulation (EU) 2024/1481 of 29 May 2024 granting a Union authorisation for the single biocidal product Nordkalk QL 0-2 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

COMMISSION IMPLEMENTING REGULATION (EU) 2024/1481
of 29 May 2024
granting a Union authorisation for the single biocidal product ‘Nordkalk QL 0-2’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
(Text with EEA relevance)
Article 1
Article 2
ANNEX
SUMMARY OF PRODUCT CHARACTERISTICS FOR A BIOCIDAL PRODUCT
1.
ADMINISTRATIVE INFORMATION
1.1.
Trade name(s) of the product
1.2.
Authorisation holder
1.3.
Manufacturer(s) of the product
1.4.
Manufacturer(s) of the active substance(s)
2.
PRODUCT COMPOSITION AND FORMULATION
2.1.
Qualitative and quantitative information on the composition of the product
2.2.
Type(s) of formulation
3.
HAZARD AND PRECAUTIONARY STATEMENTS
4.
AUTHORISED USE(S)
4.1.
Use description
4.1.1.
Use-specific instructions
4.1.2.
Use-specific risk mitigation measures
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
— 4.1.4.
Where specific to the use, the instructions for safe disposal of the product and its packaging
— 4.1.5.
Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
— 4.2.
Use description
4.2.1.
Use-specific instructions
4.2.2.
Use-specific risk mitigation measures
4.2.3.
Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment
— 4.2.4.
Where specific to the use, the instructions for safe disposal of the product and its packaging
— 4.2.5.
Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
— 4.3.
Use description
4.3.1.
Use-specific instructions
4.3.2.
Use-specific risk mitigation measures
4.3.3.
Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment
— 4.3.4.
Where specific to the use, the instructions for safe disposal of the product and its packaging
4.3.5.
Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
— 4.4.
Use description
4.4.1.
Use-specific instructions
4.4.2.
Use-specific risk mitigation measures
4.4.3.
Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment
— 4.4.4.
Where specific to the use, the instructions for safe disposal of the product and its packaging
4.4.5.
Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
— 5.
GENERAL DIRECTIONS FOR USE
(1)
5.1.
Instructions for use
5.2.
Risk mitigation measures
5.3.
Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment
5.4.
Instructions for safe disposal of the product and its packaging
5.5.
Conditions of storage and shelf-life of the product under normal conditions of storage
6.
OTHER INFORMATION