Dear Regulatory experts,
I wonder which are the applicable regulations about product disposal requirements for a small medical device battery powered to be marketed in both Europe and the US.
In the EU I understand that the following regulations applies: 2020/0353 (repealing directive 2006/66), WEE directive 2012/19/EU and 2005/32/EC, which establishes a framework for eco-design requirements energy-using products. I don't know if the regulatory framework is complete for the EU, and I miss info for the US.
Who can help?
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Mauro
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