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I.S. EN ISO 5840-1:2021

Current

Current

The latest, up-to-date edition.

Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements (ISO 5840-1:2021)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

02-21-2021

Preview

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Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

US$120.36
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Abbreviations
5 Fundamental requirements
6 Device description
7 Design verification and validation
Annex A (informative) Rationale for the provisions of ISO 5840-1
Annex B (normative) Packaging
Annex C (normative) Product labels, instructions for use, and training
Annex D (normative) Sterilization
Annex E (normative) In vitro test guidelines for paediatric devices
Annex F (informative) Corrosion assessment
Annex G (informative) Echocardiographic protocol
Annex H (informative) Assessment of implant thrombogenic and haemolytic potential
Annex I (informative) Guidelines for hydrodynamic performance characterization by steady flow testing
Annex J (normative) Durability testing
Annex K (informative) Fatigue assessment
Annex L (normative) Clinical investigation endpoints for heart valve replacement devices
Bibliography

This document is applicable to heart valve substitutes intended for implantation and provides general requirements.

Committee
TC 150
DocumentType
Standard
Pages
96
ProductNote
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
PublisherName
National Standards Authority of Ireland
Status
Current
Supersedes

Standards Relationship
ISO 5840-1:2021 Identical
EN ISO 5840-1:2021 Identical

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