ICSION complies with EN ISO 13485:2016 and is accredited by TÜV SÜD Product Service GmbH.
ICSION products are CE marked under the EU Medical Device Regulation 2017/745 (MDR) and are included in the Australian Register of Therapeutic Goods (ARTG).
Certificate of Analysis Search
To find your certificate, please enter the first four characters of your lot. i.e. B111, C012
