Smith+Nephew

Company · United Kingdom

not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts (staff, costs, accreditations) are not available for it.

positions filed

in the 665 files tracked

legislative file

of 665 tracked

with a full position paper

attached to a submission

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.

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Their record over time

Smith+Nephew filed 2 positions between 5 Oct 2025 and 28 Jul 2026, across 1 of the 665 legislative files tracked here.

2025 · 1 filed2026 · 1 filed

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 28 Jul 2026source

Smith+Nephew (S+N) welcomes the opportunity to comment on the EU Commissions proposal to strengthen competitiveness of the Medical Device sector and improve safety requirements by making them more cost-effective and proportionate. S+N particularly supports the proposed measures on digitalisation (Article 52b) and reliance/recognition (Article 108).

Smith+Nephew welcomes the opportunity to provide feedback in support of the Commissions aims to make the medical device sector more competitive and make safety requirements more cost-efficient and proportionate.

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