Greetings I am trying to determine whether our laboratory equipment is required to comply with the RoHS and WEEE Directives at this time. We do have some instruments for use as IVD and realize that they do fall under the scope of the WEEE Directive as Category 8 "Medical Devices: Laboratory Equipment for in-vitro diagnosis." However, we are not sure about our thermal cyclers, DNA sequencers, mass spectrometers, etc.
The scope currently includes Category 9 called "Monitoring and Control Instruments" and gives examples including "Measuring, weighing, or adjusting appliances for household or as laboratory equipment". Our instruments do not seem like any of the other examples for the same category, yet they do measure things. Our mass spectrometers can use flight time of ions to help determine the mass and thus the original constitution of the sample. In addition, Member States may specify laboratory equipment within their laws that support the WEEE Directive. As an example, the current Swedish WEEE laws on producer responsibility clearly states that laboratory equipment is included. Your thoughts on this subject are appreciated. Regards Joe Martin Applied Biosystems [email protected] This message is from the IEEE EMC Society Product Safety Technical Committee emc-pstc discussion list. Visit our web site at: http://www.ewh.ieee.org/soc/emcs/pstc/ To cancel your subscription, send mail to: [email protected] with the single line: unsubscribe emc-pstc For help, send mail to the list administrators: Ron Pickard: [email protected] Dave Heald: [email protected] For policy questions, send mail to: Richard Nute: [email protected] Jim Bacher: [email protected] Archive is being moved, we will announce when it is back on-line. All emc-pstc postings are archived and searchable on the web at: http://www.ieeecommunities.org/emc-pstc
