{"id":426217,"date":"2024-10-20T07:00:51","date_gmt":"2024-10-20T07:00:51","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-23-30466300-dc-2023\/"},"modified":"2024-10-26T13:15:26","modified_gmt":"2024-10-26T13:15:26","slug":"bsi-23-30466300-dc-2023","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-23-30466300-dc-2023\/","title":{"rendered":"BSI 23\/30466300 DC 2023"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
1<\/td>\n | 30466300-NC.pdf <\/td>\n<\/tr>\n | ||||||
3<\/td>\n | ISO_DIS 17256 ed.1 – id.84739 Enquiry PDF (en).pdf <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 4 General Requirements 4.1 General 4.2 Test methods and conditions 5 Materials 5.1 General 5.2 Biological assessment of gas pathways 6 Design requirements 6.1 General 6.2 Specific design requirements <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 6.3 Inlet connectors <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 6.4 Outlet connectors 7 Requirements for respiratory tubing, extension tubing and connectors supplied sterile 8 Packaging 9 Information supplied by the manufacturer 9.1 General 9.2 Information supplied by the manufacturer <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | Annex\u20acA (informative) Rationale <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | Annex\u20acB (normative) Respiratory therapy equipment and tubing connectors <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | Annex\u20acC (informative) Hazard identification for the purposes of risk assessment <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" BS ISO 17256. Anaesthetic and respiratory equipment. Respiratory therapy tubing and connectors<\/b><\/p>\n |