BS ISO 5841-2:2014
$167.15
Implants for surgery. Cardiac pacemakers – Reporting of clinical performance of populations of pulse generators or leads
Published By | Publication Date | Number of Pages |
BSI | 2014 | 38 |
This part of ISO 5841 specifies requirements for reports on the clinical performance in humans of population samples of cardiac pulse generators or leads, intended for long-term implantation, hereinafter referred to as devices. Devices to be reported has to be market approved in one or more geographies. It includes general requirements for all reports and supplementary requirements for reports on cumulative experience with devices and estimates of future clinical performance for devices, when appropriate.
Annex A provides requirements for categorizing devices. It also provides normative requirements for statistical calculations, including a discussion of application of the results obtained. As with other statistical methods, the benefit of the analytical methods in this part of ISO 5841 is limited by the size of population under consideration. Annex B gives the rationale for this part of ISO 5841.
PDF Catalog
PDF Pages | PDF Title |
---|---|
6 | Foreword |
7 | Introduction |
9 | Section sec_1 Section sec_2 Section sec_3 Section sec_3.1 Section sec_3.2 Section sec_3.3 1 Scope 2 Normative references 3 Terms and definitions |
10 | 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 |
11 | Section sec_3.15 Section sec_3.16 Section sec_3.17 Section sec_3.18 Section sec_3.19 Section sec_3.20 Section sec_3.21 |
12 | Section sec_3.22 Section sec_3.23 Section sec_3.24 Section sec_3.25 Section sec_3.26 Section sec_3.27 Section sec_3.28 Section sec_3.29 Section sec_3.30 Section sec_3.31 |
13 | Section sec_3.32 Section sec_3.33 Section sec_3.34 Section sec_3.35 Section sec_3.36 Section sec_4 Section sec_4.1 Section sec_4.2 Section sec_4.3 Section sec_4.4 Section sec_4.5 4 General requirements 4.1 Frequency of publication 4.2 Method of publication 4.3 Report organization 4.4 Criteria for inclusion and removal of reported models and device families 4.5 Source of performance report data |
14 | Section sec_4.6 Section sec_4.6.1 Section sec_4.6.2 4.6 Product performance report — Required content |
15 | Section sec_4.6.2.1 |
16 | Section sec_4.6.2.2 Section sec_4.7 Section sec_5 Section sec_5.1 4.7 Adjustment for underreported events 5 Particular reporting requirements 5.1 Reporting pulse generator performance |
17 | Section sec_5.2 Section sec_5.2.1 Table tab_1 Section sec_5.2.2 5.2 Reporting lead performance |
18 | Table tab_2 Section sec_5.2.3 |
19 | Section sec_5.2.4 Section sec_5.2.4.1 |
20 | Table tab_3 |
21 | Annex sec_A Annex sec_A.1 Annex sec_A.2 Annex sec_A.2.1 Annex sec_A.2.2 Annex A (normative) Statistical method for survival analysis and discussion of application of results obtained |
23 | Figure fig_A.1 Annex sec_A.2.3 Annex sec_A.2.3.1 |
24 | Figure fig_A.2 |
25 | Table tab_A.1 |
26 | Annex sec_A.2.3.2 Figure fig_A.3 |
27 | Annex sec_A.3 Annex sec_A.3.1 Annex sec_A.3.2 Annex sec_A.3.3 |
30 | Annex sec_B Annex sec_B.1 Annex sec_B.2 Annex B (informative) Rationale |
33 | Figure fig_B.1 Figure fig_B.2 |
34 | Reference ref_1 Reference ref_2 Reference ref_3 Reference ref_4 Reference ref_5 Reference ref_6 Reference ref_7 Reference ref_8 Reference ref_9 Reference ref_10 Reference ref_11 Reference ref_12 Reference ref_13 Reference ref_14 Reference ref_15 Reference ref_16 Bibliography |