Zimmer Biomet, a global leader in medical technology, has always supported the good intentions of all parties to implement the EU Regulation 2017/745 on medical devices (MDR) as smoothly as possible within the defined transition period. However, despite extensive efforts, the system is not functioning in its intended robust, transparent, predictable and sustainable way that maintains safety and supports innovation.
Zimmer Biomet
Company · Switzerland · EU Transparency Register 48849298417-82
Counts here are a floor, never a total: they cover the 326 consultation files tracked so far (29,503 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.
Who they are
Among the 925 companies & groups on this site, they rank #923 by legislative files engaged — a count of participation, not a measure of influence.
Declares membership of
- Member of Medtech Europe and AdvaMed. In addition Zimmer Biomet is member of several national trade associations with…
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).
- Register category
- Companies & groups
- Registered as
- Zimmer Biomet Holdings (ZBH)
- Head office
- Zug, Switzerland
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Their record over time
Zimmer Biomet filed 1 position on 6 Oct 2025, across 1 of the 326 legislative files tracked here, attaching a full position paper 1 time.
What they argued
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Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.