BSI 23/30470631 DC:2023 Edition
$13.70
BS ISO 8637-1. Extracorporeal systems for blood purification – Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
Published By | Publication Date | Number of Pages |
BSI | 2023 | 42 |
PDF Catalog
PDF Pages | PDF Title |
---|---|
7 | Foreword |
8 | Introduction |
9 | 1 Scope 2 Normative references |
10 | 3 Terms and definitions (mandatory) |
13 | 4 Requirements 4.1 Biological safety 4.2 Sterility 4.3 Non-pyrogenicity 4.4 Mechanical characteristics 4.4.1 Structural integrity |
14 | 4.4.2 Blood compartment integrity 4.4.3 Haemodialyser, haemodiafilter and haemofilter blood compartment connectors |
15 | 4.4.4 Haemodialyser and haemodiafilter dialysis fluid compartment connector |
17 | 4.4.5 Haemofilter filtrate connector 4.4.6 Haemoconcentrator blood and filtrate connectors 4.5 Performance characteristics 4.5.1 Solute clearance of haemodialysers and haemodiafilters 4.5.2 Sieving coefficient of haemodialysers, haemodiafilters, haemofilters and haemoconcentrators |
18 | 4.5.3 Ultrafiltration rate. 4.5.4 Ultrafiltration coefficient 4.5.5 Blood compartment volume 4.5.6 Blood compartment pressure drop 4.5.7 Haemodialyser and haemodiafilter endotoxin transfer 4.5.8 Expiry date |
19 | 5 Test methods 5.1 General 5.2 Biological safety and haemocompatibility 5.3 Sterility 5.4 Non-pyrogenicity |
20 | 5.5 Mechanical characteristics 5.5.1 Structural integrity 5.5.2 Blood compartment integrity 5.5.3 Haemodialyser, haemodiafilter and haemofilter blood compartment connectors 5.5.4 Haemodialyser and haemodiafilter dialysis fluid compartment connectors |
21 | 5.5.5 Haemofilter filtrate connectors 5.5.6 Haemoconcentrator blood and filtrate connectors |
24 | 5.6 Performance characteristics 5.6.1 Solute clearance of haemodialysers and haemodiafilters |
27 | 5.6.2 Sieving coefficient of haemodialysers, haemodiafilters, haemofilters and haemoconcentrators |
29 | 5.6.3 Ultrafiltration rate |
30 | 5.6.4 Ultrafiltration coefficient 5.6.5 Blood compartment volume 5.6.6 Blood compartment pressure drop |
31 | 5.6.7 Haemodialyser and haemodiafilter endotoxin transfer 6 Expiry date 7 Labelling 7.1 Labelling on the device 7.2 Labelling on unit containers |
32 | 7.3 Labelling on the outer containers |
33 | 7.4 Information to be given in the accompanying documentation |
35 | 8 Packaging |
36 | Annex€A (informative) Endotoxin transfer assessment |
42 | Bibliography |