{"id":279578,"date":"2024-10-19T18:52:27","date_gmt":"2024-10-19T18:52:27","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-11607-12017\/"},"modified":"2024-10-25T15:26:22","modified_gmt":"2024-10-25T15:26:22","slug":"bs-en-iso-11607-12017","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-11607-12017\/","title":{"rendered":"BS EN ISO 11607-1:2017"},"content":{"rendered":"
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2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Annex ZA (informative)Relationship between this European Standard and the essential requirements of Directive 93\/42\/EEC [OJ L 169] aimed to be covered <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Annex ZB (informative)Relationship between this European Standard and the essential requirements of Directive 90\/385\/EEC [OJ L 189] aimed to be covered <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | Annex ZC (informative)Relationship between this European Standard and the essential requirements of Directive 98\/79\/EC [OJ L 331] aimed to be covered <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
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41<\/td>\n | undefined <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Packaging for terminally sterilized medical devices – Requirements for materials, sterile barrier systems and packaging systems<\/b><\/p>\n |