Department for Business, Innovation and Skills
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RoHS extended to medical devices and monitoring and control instruments

From 22nd July 2014, the extent of the scope for complying with the RoHS Directive has been extended to include medical devices and monitoring and control instruments. 

From 22 July 2014 the scope of the restriction of the use of certain hazardous substances (RoHS) in electrical and electronic equipment (EEE) directive (EU Directive 2011/65/EU) was extended to cover most medical devices (EEE category 8) and monitoring and control instruments (EEEcategory 9). With some exceptions, EEE in these categories placed on the market from this date will need to comply with RoHS.

Category 8 medical devices include:

  • radiotherapy equipment
  • cardiology
  • dialysis
  • pulmonary ventilators
  • nuclear medicine
  • analysers
  • freezers
  • fertilization tests and other appliances for detecting
  • laboratory equipment for in-vitro diagnosis (although the extension does not apply to in vitro diagnostic medical devices until 22 July 2016)

The Directive does not apply to active implantable medical devices.

Category 9 monitoring and control instruments includes:

  • smoke detectors
  • heating regulators
  • thermostats
  • measuring, weighing or adjusting appliances for household or laboratory equipment
  • other monitoring and control instruments used in industrial installations

Industrial monitoring and control instruments do not fall into the scope ofRoHS until 22 July 2017.

The NMO enforcement authority is responsible for enforcing this legislation and will be undertaking compliance activities in order to ensure that those who deal in category 8 and category 9 products fulfill their obligations.

For further information contact the NMO’s enquiry service

Channel website: https://www.icaew.com

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