Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements - Amendment 1 (ISO 5840-1:2021/DAM 1:2024)

Herz- und Gefäßimplantate - Herzklappenprothesen - Teil 1: Allgemeine Anforderungen - Änderung 1 (ISO 5840-1:2021/DAM 1:2024)

Implants cardiovasculaires - Prothèses valvulaires - Partie 1: Exigences générales - Amendement 1 (ISO 5840-1:2021/DAM 1:2024)

Vsadki (implantati) za srce in ožilje - Proteze za srčno zaklopko - 1. del: Splošne zahteve - Dopolnilo A1 (ISO 5840-1:2021/DAM 1:2024)

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Status
Not Published
Publication Date
03-Sep-2025
Current Stage
4060 - Closure of enquiry - Enquiry
Start Date
01-May-2024
Completion Date
01-May-2024

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SLOVENSKI STANDARD
01-april-2024
Vsadki (implantati) za srce in ožilje - Proteze za srčno zaklopko - 1. del: Splošne
zahteve - Dopolnilo A1 (ISO 5840-1:2021/DAM 1:2024)
Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements -
Amendment 1 (ISO 5840-1:2021/DAM 1:2024)
Herz- und Gefäßimplantate - Herzklappenprothesen - Teil 1: Allgemeine Anforderungen -
Änderung 1 (ISO 5840-1:2021/DAM 1:2024)
Implants cardiovasculaires - Prothèses valvulaires - Partie 1: Exigences générales -
Amendement 1 (ISO 5840-1:2021/DAM 1:2024)
Ta slovenski standard je istoveten z: EN ISO 5840-1:2021/prA1
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

DRAFT
Amendment
ISO 5840-1:2021/
DAM 1
ISO/TC 150/SC 2
Cardiovascular implants — Cardiac
Secretariat: ANSI
valve prostheses —
Voting begins on:
Part 1:
2024-02-07
General requirements
Voting terminates on:
2024-05-01
AMENDMENT 1
Implants cardiovasculaires — Prothèses valvulaires —
Partie 1: Exigences générales
AMENDEMENT 1
ICS: 11.040.40
THIS DOCUMENT IS A DRAFT CIRCULATED
FOR COMMENTS AND APPROVAL. IT
IS THEREFORE SUBJECT TO CHANGE
AND MAY NOT BE REFERRED TO AS AN
INTERNATIONAL STANDARD UNTIL
PUBLISHED AS SUCH.
This document is circulated as received from the committee secretariat.
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Reference number
ISO 5840-1:2021/DAM 1:2024(en)
DRAFT
ISO 5840-1:2021/DAM 1:2024(en)
Amendment
ISO 5840-1:2021/
DAM 1
ISO/TC 150/SC 2
Cardiovascular implants — Cardiac
Secretariat: ANSI
valve prostheses —
Voting begins on:
Part 1:
General requirements
Voting terminates on:
AMENDMENT 1
Implants cardiovasculaires — Prothèses valvulaires —
Partie 1: Exigences générales
AMENDEMENT 1
ICS: 11.040.40
THIS DOCUMENT IS A DRAFT CIRCULATED
FOR COMMENTS AND APPROVAL. IT
IS THEREFORE SUBJECT TO CHANGE
AND MAY NOT BE REFERRED TO AS AN
INTERNATIONAL STANDARD UNTIL
PUBLISHED AS SUCH.
This document is circulated as received from the committee secretariat.
IN ADDITION TO THEIR EVALUATION AS
BEING ACCEPTABLE FOR INDUSTRIAL,
© ISO 2024
TECHNOLOGICAL, COMMERCIAL AND
USER PURPOSES, DRAFT INTERNATIONAL
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
STANDARDS MAY ON OCCASION HAVE TO
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Website: www.iso.org
Published in Switzerland Reference number
ISO 5840-1:2021/DAM 1:2023(en)
ii
ISO 5840-1:2021/DAM 1:2023(en)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out through
ISO technical committees. Each member body interested in a subject for which a technical committee
has been established has the right to be represented on that committee. International organizations,
governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely
with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are described
in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the different types
of ISO documents should be noted. This document was drafted in accordance with the editorial rules of the
ISO/IEC Directives, Part 2 (see www.iso.org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of any patent
rights identified during the development of the document will be in the Introduction and/or on the ISO list of
patent declarations received (see www.iso.org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and expressions
related to conformity assessment, as well as information about ISO's adherence to the World Trade
Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/iso/foreword.html.
This document was prepared by ISO/TC 150, Implants for surgery, Subcommittee 2, Cardiovascular implants
and extracorporeal system.
The main changes are as follows:
— Corrections and clarifications to ISO 5840-1:2021
A list of all parts in the ISO 5840 series can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www.iso.org/members.html.

iii
ISO 5840-1:2021/DAM 1:2023(en)
Cardiovascular implants — Cardiac valve prostheses —
Part 1:
General requirements
AMENDMENT 1
Terms and definitions
3.1
Replace the definition of accessory with the
...

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