These pages provide technical information on our products with regard to the new Medical Devices Regulation (MDR 2017/745) which came into effect on 26th May 2021.
TwoXTen (formerly HouseMate – Lite)
Obligations for our resellers
If you import any medical device products into the EU please make yourself aware of Article 13 – Obligations of importers in the regulations.
If you sell any medical device products to distributors within any EU country, we recommend you alert them to Article 14 – General obligations of distributors.