Battery Regulation
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Table of Contents
Chapter I – General provisions
Chapter II – Sustainability and safety requirements
Chapter III – Labelling, marking and information requirements
Chapter IV – Conformity of batteries
Chapter V – Notification of conformity assessment bodies
Chapter VI – Obligations of economic operators other than the obligations in Chapters VII and VIII
Chapter VII – Obligations of economic operators as regards battery due diligence policies
Chapter VIII – Management of waste batteries
Chapter IX – Digital battery passport
Chapter X – Union market surveillance and Union safeguard procedures
Chapter XI – Green public procurement and procedure for amending restrictions on substances
Chapter XII – Delegated powers and committee procedure
Chapter XIII – Amendments
Chapter XIV – Final provisions
Recitals (143)
Annexes
Recital 38
(38) In order to ensure that portable batteries that were incorporated into appliances are subject to separate collection, treatment and high quality recycling once those appliances become waste, provisions to ensure the removability and replaceability of batteries in such appliances are necessary. Consumer safety should be ensured, in line with Union law and in particular Union safety standards, during the removal of portable batteries from or the replacement of portable batteries in an appliance. A portable battery should be considered to be removable by the end-user when it can be removed with the use of commercially available tools and without requiring the use of specialised tools, unless they are provided free of charge, or proprietary tools, thermal energy or solvents to disassemble it. Commercially available tools are considered to be tools available on the market to all end-users without the need for them to provide evidence of any proprietary rights and that can be used with no restriction, except health and safety-related restrictions. The general provisions of this Regulation should apply without prejudice to the safety and maintenance requirements for professional medical imaging and radiotherapy devices as defined in Medical Devices Regulation (MDR) of the European Parliament and of the Council and for in vitro diagnostic medical devices as defined in In Vitro Diagnostic Regulation (IVDR) of the European Parliament and of the Council , and could be complemented with requirements laid down for particular products powered by batteries under implementing measures under Directive 2009/125/EC. Where other Union law lays down more specific requirements, for safety reasons, regarding the removal of batteries from products, such as toys, those specific rules should apply.
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