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Medical Devices fell within the scope of the RoHS2 Directive 2011/65/EU on 22 July 2014. Most Medical Device (category 8) manufacturers have met the deadline (only just in some cases), but they have known that compliance would have been necessary since 2006 when  ERA Technology published a report on Categories  8 (medical devices) and 9 (monitoring and control instruments) on behalf of the European Commission. However, compliance has only been achieved with the acceptance of many add ...