Advice
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.