The EU Directive 2012/19/EC on Waste Electrical and Electronic Equipment (also known as WEEE II) represents the EU’s latest effort to increase recycling of and reduce waste from electrical and electronic equipment. Under the EU WEEE, EU Member States must achieve collection rates of 45% beginning in 2016 and collection rates of 65% by 2019. Most important, all categories of electrical and electronic equipment, including medical devices and in-vitro medical devices, will be subject to WEEE II recovery targets by 13 August 2012.
In order to achieveEU WEEE Directive compliance, manufactures (otherwise known as producers in WEEE II) are required to establish processes and systems to ensure the safe and effective collection and recovery of most electrical and electronic waste. Medical devices such as in vitro diagnostic medical devices, where such devices are expected to be infective prior to end of life, and active implantable medical devices are excluded from the scope of WEEE II.
Manufacturers are also encouraged to maximize the use of recoverable and recyclable materials in their products, and to design products in order to facilitate the dismantling and recovery of recyclable materials. Manufacturers are required to appoint an authorized representative in each EU Member State, who is legally responsible for fulfilling the manufacturer’s responsibilities under WEEE II.
In addition to the requirements of WEEE II, medical device manufactures may be subject to other EU directives and regulations addressing the control and recycling of electrical and electronic waste. These include EU Directive 2011/65/EU on the restriction of the use of hazardous substances (RoHS II), and as well as the EU directive on the disposal of batteries and on product packaging and packaging waste.