{"standard":"EN ISO 18562-1","listings":[{"edition":"EN ISO 18562-1:2024","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 1: Evaluation and testing within a risk management process (ISO 18562-1:2024)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"}],"events":[{"date":"2026-01-30","type":"added","ref":"EN ISO 18562-1:2024","leg_slug":"mdr","leg_name":"Medical Devices Regulation"}],"generated":"2026-08-16 23:54 UTC"}