{"id":277711,"date":"2024-10-19T18:42:13","date_gmt":"2024-10-19T18:42:13","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-146022011\/"},"modified":"2024-10-25T15:13:23","modified_gmt":"2024-10-25T15:13:23","slug":"bs-en-iso-146022011","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-146022011\/","title":{"rendered":"BS EN ISO 14602:2011"},"content":{"rendered":"
ISO 14602:2010 specifies particular requirements for non-active surgical Implants for osteosynthesis, referred to as implants. In addition to ISO 14630, ISO 14602:2010 gives particular requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging and information supplied by the manufacturer.<\/p>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
11<\/td>\n | Scope Normative references Terms and definitions Intended performance General <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | Intended purpose Functional characteristics <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | Intended conditions of use Design attributes <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | Materials Design evaluation General Pre-clinical evaluation Clinical evaluation Post-market surveillance <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | Manufacturing Sterilization Packaging Information supplied by manufacturer General Labelling Instructions for use Restrictions on combinations Marking on implant Marking for special purposes <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Non-active surgical implants. Implants for osteosynthesis. Particular requirements<\/b><\/p>\n |