The European Hearing Instrument Manufacturers Association (EHIMA) welcomes the opportunity to contribute to the European Commissions stakeholder consultation on the Digital Omnibus Package. The Package presents an important opportunity to streamline existing legislation, eliminate redundancies, and ensure that the combined effect of digital regulations, including the AI Act, the Data Act, and relat-ed frameworks…
EHI
EHIMA
Industry association · Belgium · EU Transparency Register 34590331316-73
3
positions filed
in the 665 files tracked
2
legislative files
of 665 tracked
3
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.
Who they are
Among the 1518 trade and business associations on this site, they rank #968 by legislative files engaged, a count of participation, not a measure of influence.
1.8
declared lobbying FTE
self-declared
€50K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2009
in the register since
Declares membership of
- The organization is a member of the World Hearing Forum of the World Health Organization (https://www.who.int/activit…
- The organization is the provider of the international information portal www.hearingyou.org
Self-declared to the EU Transparency Register (snapshot 14 Oct 2026).
- Register category
- Trade and business associations
- Registered as
- European Hearing Instrument Manufacturers Association (EHIMA)
- Head office
- Frankfurt am Main, Germany
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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Their record over time
EHIMA filed 3 positions between 26 Sept 2025 and 11 May 2026, across 2 of the 665 legislative files tracked here, attaching a full position paper 3 times.
2025 · 2 filed2026 · 1 filed
What they argued
EHIMA welcomes the European Commissions targeted MDR revision and appreciates the opportunity to contribute to this important consultation. EHIMA supports the Commissions efforts to strengthen efficiency, proportionality and legal certainty while maintaining high patient safety standards. The input focuses on reducing fragmentation, improving predictability, and ensuring balanced AI and cybersecurity requirements.
As set out in our earlier submission, the European Hearing Instrument Manufacturers Association (EHIMA) welcomes the opportunity to contribute to the European Commissions stakeholder consultation on the revision of the Medical Device Regulation (MDR). EHIMA urges the European Commission to revise MDR implementation to ensure efficiency, consistency, and risk-based regulation.
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Turns up on the same files
Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers, not evidence of coordination, and we do not suggest any.
Showing 5 of 38.
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Everything on this page comes from EHIMA’s own submissions to the European Commission. We have added nothing and interpreted nothing. If something is wrong or out of date, email info@policyspeak.com and we will correct it. If you are an individual named in a record, our privacy policy sets out your rights to correction, objection and removal.
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.