Industry association · France · EU Transparency Register 221611926851-83
Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.
Among the 410 trade unions and professional associations on this site, they rank #143 by legislative files engaged, a count of participation, not a measure of influence.
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Snitem filed 5 positions between 18 Jan 2023 and 31 Jul 2026, across 4 of the 665 legislative files tracked here, attaching a full position paper 1 time.
The Snitem thanks the European Commission for giving it the opportunity to give its opinion on the proposal for a Digital Omnibus Regulation, which represents a timely initiative to simplify the EU’s digital regulatory framework, reduce the administrative burden and strengthen the competitiveness of European organisations.
Filed in French · English published by the European Commission
The Snitem welcomes the proposal for a targeted revision of the Medical Devices Regulation. This initiative responds to several challenges identified since the entry into application of the Regulation and is an important step to restore the predictability of the European regulatory framework, strengthen patients’ access to innovations and support the competitiveness of the European medical technology industry, while…
Filed in French · English published by the European Commission
The Syndicat National de l’Industrie des Technologies Medical (Snitem) brings together in France the players in the medical technology and devices industry, including companies involved in digital health. It brings together 630 French or international companies, most of which are SMEs or DETI.
Filed in French · English published by the European Commission
The Snitem (National Medical Technology Industry Union) takes note of the European Commission’s proposal to adapt the transitional measures of Regulation (EU) 2017/745 on medical devices and welcomes its recognition of the urgent and persistent risks of shortages of medical devices in Europe resulting from the implementation challenges of the Regulation.
Filed in French · English published by the European Commission
Snitem supports Medtech Europe's position : MedTech Europe welcomes the European Commission public consultation on the draft Implementing act according to Art. 24(3) to lay down the details and format for the Art. 24- disclosure of information requirement and possibility to comment on the requirement to disclose information on unsold consumer products.
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