Hello! everyone!
I am learning that some substances are added in appendices of Annex XVII of REACH regulation in Dec.2021. However, I did not find the added substances in the restriction substances list from ECHA website.
Could you please kindly help me to figure out the relationship between the appendices to Annex XVII and Annex VII? Or could you please kindly show me that how to comply with the requirement of these appendices as a non-European medical device manufacturer?
Thank you in advance!
I am learning that some substances are added in appendices of Annex XVII of REACH regulation in Dec.2021. However, I did not find the added substances in the restriction substances list from ECHA website.
Could you please kindly help me to figure out the relationship between the appendices to Annex XVII and Annex VII? Or could you please kindly show me that how to comply with the requirement of these appendices as a non-European medical device manufacturer?
Thank you in advance!
