{"url": "https://sub.xiliary.com/p/brendancodykenny/posts/43/commercial-copies-of-the-eu-medical-device-register-differ", "author": {"handle": "brendancodykenny", "name": "Brendan Cody-Kenny", "headline": "Technical Due Diligence for Software M&A", "url": "https://sub.xiliary.com/p/brendancodykenny"}, "post": {"id": 43, "url": "https://sub.xiliary.com/p/brendancodykenny/posts/43/commercial-copies-of-the-eu-medical-device-register-differ", "kind": "update", "summary": "Commercial copies of the EU medical device register differ from the official one, so I check every diligence claim against EUDAMED itself.", "details": ["EUDAMED is the EU's official database of medical device companies and their products.", "Authorised representatives, the EU contacts that non-EU makers must name, only confirm their records every two years.", "59.5% of them have no devices registered, so a company showing zero devices is not a red flag on its own."], "links": [], "tags": ["due-diligence", "regulatory-data", "research-method"], "happened_on": null, "created": "2026-10-01T20:45:01.041361Z", "edited": "2026-10-02T05:21:33.394154Z"}}