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BS EN ISO 5840-1:2015

$198.66

Cardiovascular implants. Cardiac valve prostheses – General requirements

Published By Publication Date Number of Pages
BSI 2015 68
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PDF Pages PDF Title
4 European foreword
5 Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC on medical devices
Table ZA.1 — Correspondence between this European Standard and Directive 93/42/EEC on medical devices
7 Foreword
8 Introduction
10 1 Scope
2 Normative references
11 3 Terms and definitions
20 4 Abbreviations
21 5 Fundamental requirements
6 Device description
6.1 Intended use
6.2 Design inputs
6.2.1 Operational specifications
6.2.2 Performance specifications
6.2.3 Implant procedure
22 6.2.4 Packaging, labelling, and sterilization
6.3 Design outputs
23 6.4 Design transfer (manufacturing verification/validation)
6.5 Risk management
24 7 Design verification testing and analysis/design validation
7.1 General requirements
7.2 In vitro assessment
7.3 Preclinical in vivo evaluation
7.4 Clinical investigations
25 Annex A (informative) Rationale for the provisions of this part of ISO 5480
28 Annex B (normative) Packaging
29 Annex C (normative) Product labels, instructions for use, and training
32 Annex D (normative) Sterilization
33 Annex E (informative) In vitro test guidelines for paediatric devices
37 Annex F (informative) Statistical procedures when using in vitro performance criteria
38 Annex G (informative) Examples and definitions of some physical and material properties of heart valve systems
49 Annex H (informative) Examples of standards applicable to testing of materials and components of heart valve systems
55 Annex I (informative) Raw and post-conditioning mechanical properties for support structure materials
57 Annex J (informative) Corrosion assessment
60 Annex K (informative) Echocardiographic protocol
63 Bibliography
BS EN ISO 5840-1:2015
$198.66