Complete the device description wizard
Review the generated description, correct its facts and produce the available PDF record.
Classification and device facts
Where to find it
My Cases → Your case → Review Device Description
You need
- A case that has reached client review of its device description.
- Open it from the case's status action, "Review Device Description".
- Read the description against the actual device and intended purpose — "Preview document" in the header shows the PDF at any point.
- Correct or confirm the requested information.
- On the "Final review" step choose "Confirm & lock". The wizard then closes back to the case; the preview is no longer available from here once locked.
What happens next
- The case advances to regulatory strategy work after the description is confirmed.
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Official references
This article is practical product guidance, not legal advice. Confirm regulatory deadlines and obligations against current official sources and your assigned expert.
European Commission — Medical Devices: New regulationsRegulation (EU) 2017/745 — Medical Device RegulationRegulation (EU) 2017/746 — In Vitro Diagnostic Medical Devices