EUDAMED and publication inputs may include device identifiers, manufacturer details, authorized representative information, risk class, certificates, intended purpose, device description, and SSCP-related material where applicable.
Public-facing summaries should be consistent with the technical file but written for the intended audience. For patient-facing content, clarity matters as much as regulatory completeness.
If a notified body or authority requires a specific format, upload the correspondence or template so Complya and your expert can align the output to that expectation.
Official references
This article is practical product guidance, not legal advice. Confirm regulatory deadlines and obligations against current official sources and your assigned expert.