BS EN ISO 10079-1:2015:2016 Edition
$167.15
Medical suction equipment – Electrically powered suction equipment
Published By | Publication Date | Number of Pages |
BSI | 2016 | 42 |
PDF Catalog
PDF Pages | PDF Title |
---|---|
11 | 1 Scope 2 Normative references |
12 | 3 Terms and definitions |
14 | 4 General requirements 4.1 Risk management |
15 | 4.2 Usability 4.3 Clinical investigation 4.4 Biophysical or modelling research 4.5 Test methods 5 Cleaning, disinfection and sterilization |
16 | 6 Design requirements 6.1 Collection container 6.1.1 General 6.1.2 Container capacity 6.1.3 Container strength 6.2 Connections 6.2.1 Tubing connectors for collection containers |
17 | 6.2.2 Inlet port 6.2.3 Exhaust port 6.3 Suction tubing 6.4 Vacuum level indicators |
18 | 6.5 Spillage on electrical suction equipment 7 Operational requirements 7.1 Ease of operation 7.2 Dismantling and reassembly 7.3 Mechanical shock 7.4 Stability |
19 | 7.5 Protective devices 7.5.1 Contamination protection 7.5.2 Overfill protection devices 7.5.3 Pressure protection 7.6 Noise 7.6.1 Low vacuum/low flowrate equipment 7.6.2 Suction equipment other than that specified in 7.6.1 |
20 | 7.7 Air leakage 7.7.1 Collection containers for general use 7.7.2 Collection containers for thoracic drainage 8 Physical requirements for suction equipment for field use 8.1 (*) Dimensions 8.2 Mass 9 Performance requirements for vacuum level and flowrate 9.1 High vacuum/high flowrate equipment |
21 | 9.2 Medium vacuum equipment 9.3 Low vacuum/low flowrate equipment 9.4 Low vacuum/high flowrate equipment 9.5 Thoracic drainage equipment for adults 9.6 Intermittent vacuum equipment 9.7 Vacuum regulators with fixed setting |
22 | 9.8 Vacuum regulators with variable setting 9.9 Equipment intended for pharyngeal suction 9.10 Battery powered transportable suction equipment 9.11 Interruption of the power supply 10 (*) Resistance to environment of suction equipment for field and/or transport use 10.1 Operating conditions 10.2 Storage |
23 | 11 Information to be supplied by the manufacturer (labelling and instructions for use) 11.1 Information supplied by the manufacturer shall comply with EN 1041. 11.3 Labelling of equipment |
24 | 11.4 Instructions for use |
26 | Annex A (normative) Test methods |
37 | Annex B (informative) Rationale statement |
38 | Annex C (informative) Lumen size and its effect on flowrate |
39 | Annex D (informative) Schematic of suction equipment |
40 | Bibliography |