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Medical Devices

Non-medical products

From 26 May 2021, all non-medical devices in Annex XVI must be CE marked in order to be placed on the market and thus comply with the provisions of the Medical Devices Regulation 2017/745.

List of groups of products without an intended medical purpose referred to in ANNEX XVI that require a CE marking are:

  1. Contact lenses or other items intended to be introduced into or onto the eye.
  2. Products intended to be totally or partially introduced into the human body through surgically invasive means for the purpose of modifying the anatomy or fixation of body parts with the exception of tattooing products and piercings.
  3. Substances, combinations of substances, or items intended to be used for facial or other dermal or mucous membrane filling by subcutaneous, submucous or intradermal injection or other introduction, excluding those for tattooing.
  4. Equipment intended to be used to reduce, remove or destroy adipose tissue, such as equipment for liposuction, lipolysis or lipoplasty.
  5. High intensity electromagnetic radiation (e.g. infra-red, visible light and ultra-violet) emitting equipment intended for use on the human body, including coherent and non-coherent sources, monochromatic and broad spectrum, such as lasers and intense pulsed light equipment, for skin resurfacing, tattoo or hair removal or other skin treatment.
  6. Equipment intended for brain stimulation that apply electrical currents or magnetic or electromagnetic fields that penetrate the cranium to modify neuronal activity in the brain.

At Azierta, we have a team of professionals with extensive experience and we support manufacturers in obtaining the CE mark and in contacting Notification Bodies.  


For further information click here.

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