swissdamed Readiness Check
Check whether your actor and product registrations in swissdamed are correctly set up under the Swiss Medical Devices Ordinance (MedDO, SR 812.213). Device registration has been mandatory since 1 July 2026, with a transitional period until 31 December 2026. swissdamed is independent of EUDAMED: EU registration does not cover the Swiss market.
Question 1 of 5
Have you appointed a Swiss authorized representative (CH-REP) for the Swiss market?
CH-REP obligation, MedDO (SR 812.213) Art. 56.
Orientation only, not a substitute for a regulatory assessment.
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