CMC supports manufacturers in Swissdamed registration and UDI management for medical devices and IVDs in Switzerland, ensuring a compliant, efficient process aligned with regulatory deadlines.
CMC supports manufacturers in obtaining Swissdamed registration for medical devices and IVD products in Switzerland, including the mandatory registration of UDI (Unique Device Identification) in the swissdamed national database. Swissdamed registration is scheduled to become mandatory on 1st July 2026, with a transitional period until 31st December 2026 for most devices placed on the Swiss market.
We can support you with UDI data submission and compliance with swissdamed requirements.
With CMC’s expertise, you can ensure a compliant, efficient registration process and a successful market placement in Switzerland.
Choose CMC to obtain your Swissdamed registration
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