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X-WR-CALDESC:We Create Compliance for Safer Markets
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DTSTART:20260329T030000
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DTSTART;TZID=Europe/Brussels:20260701T000000
DTEND;TZID=Europe/Brussels:20270101T000000
DTSTAMP:20261009T073019Z
CREATED:20261009
LAST-MODIFIED:20261009
PRIORITY:5
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SUMMARY:Swissdamed device registration becomes mandatory
DESCRIPTION:\n\nFrom 1 July 2026, manufacturers placing medical devices and IVDs on the Swiss market must ensure their devices are registered in swissdamed ( https://mdlaw.eu/switzerland/swissdamed-device-registration-becomes-mandatory-from-1-july-2026/ ), Switzerland’s national medical device database managed by Swissmedic.\n\n\n\nThe deadline introduces new registration and compliance responsibilities for both manufacturers and their Swiss Authorised Representatives, making swissdamed registration an essential part of maintaining access to the Swiss market.\n\n\n\nEconomic operators have until 31 December 2026 to complete existing device registrations. However, devices subject to vigilance reporting must be registered without delay and cannot benefit from this transition period.\n\n\n\nFor manufacturers established outside Switzerland, registration is handled through their Swiss Authorised Representative (CH-REP).\n\n\n\nNeed support preparing for the swissdamed registration deadline? Whether you need a Swiss Authorised Representative (CH-REP) or assistance with device registration, get in touch with us to ensure your devices remain compliant on the Swiss market.\n\n\n\n \n\n
URL:https://www.obelis.net/events/swissdamed-registration-deadline-2026/
CATEGORIES:Deadlines
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