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X-WR-CALDESC:Events for Obelis Group
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DTSTART;TZID=Europe/Brussels:20260701T000000
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CREATED:20260904T083808Z
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UID:10000064-1782864000-1798761599@www.obelis.net
SUMMARY:Swissdamed device registration becomes mandatory
DESCRIPTION:From 1 July 2026\, manufacturers placing medical devices and IVDs on the Swiss market must ensure their devices are registered in swissdamed\, 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.
URL:https://www.obelis.net/events/swissdamed-registration-deadline-2026/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/09/Deadline-swissdamed-1-1.jpg
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DTSTART;TZID=Europe/Brussels:20260731T000000
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DTSTAMP:20260420T151517Z
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UID:10000046-1785456000-1785542399@www.obelis.net
SUMMARY:EU Fragrance Allergens Deadline
DESCRIPTION:Starting on 31 July 2026\, cosmetic products placed on the EU market must comply with the updated labelling requirements\, including the disclosure of 56 additional fragrance allergens where applicable. \n\n\n\nFrom this date onwards: \n\n\n\n✅ Products that do not meet the updated labelling requirements may be held at customs\, refused entry\, or removed from the market \n\n\n\n✅ Every new product entering EU customs is treated as a fresh placement on the market; consequently\, all batches arriving after the deadline must meet the updated labeling requirements\, regardless of whether the product was previously available. \n\n\n\nNeed a tailored assessment or product-specific guidance? Our experts are here to help.Not sure if your products are compliant? Contact Obelis for a detailed evaluation.
URL:https://www.obelis.net/events/eu-cosmetics-fragrance-allergens-deadline-2026-labeling-compliance/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/04/Deadline-fragrance-1.jpg
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DTSTART;TZID=Europe/Brussels:20261127T000000
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DTSTAMP:20260904T095911Z
CREATED:20260904T095908Z
LAST-MODIFIED:20260904T095911Z
UID:10000065-1795737600-1795823999@www.obelis.net
SUMMARY:EUDAMED Deadline
DESCRIPTION:Commission Decision (EU) 2025/2371 triggered the transition period leading to the 27 November 2026 deadline for the registration of legacy devices in EUDAMED. \n\n\n\nWith the deadline approaching\, manufacturers should ensure that the required device information is complete\, accurate\, and ready for registration. This involves more than entering data into EUDAMED: product and UDI information must be correctly aligned with actor registration (SRN)\, certification data\, and the relevant EUDAMED modules. \n\n\n\nManufacturers should use the remaining transition period to identify data gaps\, validate existing information\, and clarify the responsibilities of manufacturers\, Authorized Representatives\, and Notified Bodies. \n\n\n\nNeed support preparing for the EUDAMED deadline? Get in touch with us to ensure your registrations are completed correctly and on time.
URL:https://www.obelis.net/events/eudamed-legacy-device-registration-deadline-2026/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/09/Deadline-Eudamed-1.jpg
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