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AMD

Association of Medical Device Reprocessors

Industry association · Germany · EU Transparency Register 884250338262-72

1
position filed
in the 326 files tracked
1
legislative file
of 326 tracked
1
with a full position paper
attached to a submission

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 1205 trade and business associations on this site, they rank #866 by legislative files engaged — a count of participation, not a measure of influence.

0.2
declared lobbying FTE
self-declared
€100K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2020
in the register since

Declares membership of

  • AMDR is a member of:
  • the standard setting organization, the Association for the Advancement of Medical Instrumentation:https://www.aami.org/
  • the Remanufacturing Association Alliance: http://www.remancouncil.org/collaborate/partnerships/remanufacturing-associ…
  • and

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).

Register category
Trade and business associations
Head office
Washington, United states
EU office
Berlin

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

Association of Medical Device Reprocessors filed 1 position on 18 Sept 2025, across 1 of the 326 legislative files tracked here, attaching a full position paper 1 time.

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 18 Sept 2025PDFsource

The Association of Medical Device Reprocessors, AMDR, respectfully submits feedback with regard to Article 17, or the single-use device reprocessing provisions. Consistent with this call for evidences objectives, we strongly urge the Commission to recommend a simplification of Article 17.1 to reduce the needless and disproportionate burden placed on innovative, circular reprocessed or remanufactured devices.

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Everything on this page comes from Association of Medical Device Reprocessors’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.