Regulatory information

Regulatory information

Aidoc: head is a CE-marked class 1 medical device.

e‑CTA is a CE-marked class 2a medical device.

Icobrain Ix is a CE-marked class 1 medical device.

qER is a CE-marked class 1 medical device.

Zebra triage is a CE-marked class 1 medical device.

These and related technologies are likely to become class 2 devices during the transition from the Medical Device Directive to the Medical Device Regulation from May 2020 onwards.