Working with a client to introduce a next generation of electro-mechanical medical device into the EU. In preparation, we recently had RoHS, WEEE and REACH assessments done by our 60601 testing house. We were surprised at the number of components that failed or are shown at high risk of failing compliance in their final assessment. Many of them because the component supplier could not or would not provide supplier or material declarations. Has anyone faced similar issues? Do you know of an independent consultant that could advise us on next steps? Any help or referral appreciated. Thanks.