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I.S. EN ISO 5840-3:2021

Current

Current

The latest, up-to-date edition.

Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques (ISO 5840-3:2021)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

21-02-2021

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

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


Dates of withdrawal of national standards are available from NSAI.

€88.00
Excluding VAT

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) Description of the transcatheter heart valve system
Annex B (informative) Transcatheter heart valve substitute hazard analysis example
Annex C (informative) Guidelines for verification of hydrodynamic performance —
Annex D (normative) Requirements for delivery system design and evaluation
Annex E (informative) Examples of design specific testing
Annex F (informative) Preclinical in vivo evaluation
Annex G (normative) Adverse event classification during clinical investigation
Annex H (informative) Multimodality imaging of TAVI and TMVI pre, peri and postimplantation
Bibliography

This document is applicable to all devices intended for implantation as a transcatheter heart valve substitute.

Committee
TC 150
DocumentType
Standard
Pages
74
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 5840-3:2021 Identical
EN ISO 5840-3:2021 Identical

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