{"id":277720,"date":"2024-10-19T18:42:16","date_gmt":"2024-10-19T18:42:16","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-10079-22014\/"},"modified":"2024-10-25T15:13:25","modified_gmt":"2024-10-25T15:13:25","slug":"bs-en-iso-10079-22014","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-10079-22014\/","title":{"rendered":"BS EN ISO 10079-2:2014"},"content":{"rendered":"
This part of ISO 10079 specifies safety and performance requirements for manually powered suction equipment intended for oro-pharyngeal suction. It applies to equipment operated by foot or by hand or both. Annex D illustrates the three parts of ISO 10079 by providing a schematic for typical systems.<\/p>\n
The commonest use of manually powered suction is in situations outside of health care settings often described as field use or transport use. Use in these situations may involve extreme conditions of weather or terrain. Additional requirements for suction equipment intended for field and\/or transport use are included in this part of ISO 10079.<\/p>\n
This part of ISO 10079 does not apply to the following:<\/p>\n
end pieces such as suction catheters, Yankauer sucker and suction tips;<\/p>\n<\/li>\n
dental suction equipment;<\/p>\n<\/li>\n
mucus extractors, including neonatal mucus extractors.<\/p>\n<\/li>\n<\/ol>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
4<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
5<\/td>\n | Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93\/42\/EEC Table ZA.1 \u2014 Correspondence between this European Standard and Directive 93\/42\/EEC <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | Section sec_1 Section sec_2 Section sec_3 1\tScope 2\tNormative references 3\tTerms and definitions <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | Section sec_3.1 Section sec_3.2 Section sec_3.3 Section sec_3.4 Section sec_3.5 Section sec_3.6 Section sec_3.7 Section sec_3.8 Section sec_3.9 Section sec_3.10 Section sec_3.11 Section sec_3.12 Section sec_3.13 Section sec_3.14 <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | Section sec_3.15 Section sec_3.16 Section sec_3.17 Section sec_4 Section sec_4.1 Section sec_4.1.1 Section sec_4.1.2 Section sec_4.1.3 Section sec_4.1.4 4\tGeneral requirements 4.1\tRisk management <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | Section sec_4.2 Section sec_4.3 Section sec_4.4 Section sec_5 Section sec_6 Section sec_6.1 Section sec_6.1.1 Section sec_6.1.2 4.2\tUsability 4.3\tClinical investigation 4.4\tBiophysical or modelling research 5\tCleaning, disinfection and sterilization 6\tDesign requirements 6.1\tCollection container <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | Section sec_6.1.3 Section sec_6.2 Section sec_6.2.1 Section sec_6.2.2 Section sec_6.2.3 Section sec_6.3 6.2\tConnections 6.3\tSuction tubing <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | Section sec_6.4 Section sec_7 Section sec_7.1 Section sec_7.2 Section sec_7.3 Section sec_7.4 Section sec_7.4.1 6.4\tVacuum level indicators 7\tOperational requirements 7.1\tEase of operation 7.2\tDismantling and reassembly 7.3\tMechanical shock 7.4\tStability <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | Section sec_7.4.2 Section sec_7.5 Section sec_7.5.1 Section sec_7.5.2 Section sec_7.6 Section sec_8 Section sec_8.1 Section sec_8.2 7.5\tProtection devices 7.6\tImmersion in water 8\tPhysical requirements for field and transport use suction equipment 8.1\t(*)Dimensions 8.2\tMass <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | Section sec_9 Section sec_9.1 Section sec_9.2 Section sec_9.3 Section sec_10 Section sec_10.1 Section sec_10.2 Section sec_11 Section sec_11.1 Section sec_11.2 9\tPerformance requirements for vacuum level and flowrate 9.1\tVacuum level 9.2\tFree air flowrate 9.3\tPharyngeal suction 10\t(*)Resistance to environment of suction equipment for field and\/or transport use 10.1\tOperating conditions 10.2\tStorage 11\tMarking 11.1\tUse of symbols 11.2\tEquipment <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | Section sec_11.3 Section sec_12 11.3\tEquipment or carrying case 12\tInformation to be supplied by the manufacturer <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | Annex sec_A Annex sec_A.1 Annex sec_A.2 Annex sec_A.2.1 Annex sec_A.2.2 Annex sec_A.3 Annex\u00a0A \n(normative)<\/p>\n Test methods <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | Table tab_a Figure fig_A.1 Annex sec_A.4 <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | Table tab_b Figure fig_A.2 Annex sec_A.5 <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | Annex sec_A.6 Annex sec_A.7 Annex sec_A.8 Table tab_c Figure fig_A.3 <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | Annex sec_A.9 Annex sec_A.9.1 Annex sec_A.9.1.1 Annex sec_A.9.1.2 Annex sec_A.9.2 Annex sec_A.10 Annex sec_A.10.1 Annex sec_A.10.2 Annex sec_A.10.2.1 Annex sec_A.10.2.2 Annex sec_A.10.2.3 <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | Annex sec_A.10.2.4 <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | Annex sec_B Annex sec_B.1 Annex sec_B.2 Annex sec_B.3 Annex sec_B.4 Annex sec_B.5 Annex\u00a0B \n(informative)<\/p>\n Rationale statement <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | Annex sec_C Table tab_C.1 Annex\u00a0C \n(informative)<\/p>\n Lumen size and its effect on flowrate <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | Annex sec_D Table tab_d Figure fig_D.1 Annex\u00a0D \n(informative)<\/p>\n Schematic of suction equipment Schematic of suction equipment <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | Reference ref_1 Reference ref_2 Reference ref_3 Reference ref_4 Bibliography Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Medical suction equipment – Manually powered suction equipment<\/b><\/p>\n |