SIST EN ISO 80601-2-67:2021
(Main)Medical electrical equipment - Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment (ISO 80601-2-67:2020)
Medical electrical equipment - Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment (ISO 80601-2-67:2020)
This particular standard is applicable to the basic safety and essential performance of oxygen conserving equipment, hereafter referred to as me equipment, in combination with its accessories intended to conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is typically used by a lay operator.
This particular standard is also applicable to those accessories intended by their manufacturer to be connected to conserving equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the conserving equipment.
This particular standard is only applicable to active devices (e.g. Pneumatically or electrically powered) and is not applicable to non-active devices (e.g. Reservoir cannulas).
Medizinische elektrische Geräte- - Teil 2-67: Besondere Festlegungen für die Basissicherheit einschließlich der wesentlichen Leistungsmerkmale von Sauerstoff-Dosiergeräten ISO 80601-2-67:2020)
Dieses Dokument gilt für die Basissicherheit und die wesentlichen Leistungsmerkmale eines Dosiergeräts für Sauerstoff, nachfolgend als ME-Gerät bezeichnet, das zusammen mit dessen Zubehör dafür vorgesehen ist, durch unterbrochene und mit dem Inspirationszyklus des Patienten abgestimmte Abgabe von Gas beim Gebrauch in der medizinischen Versorgung in häuslicher Umgebung Supplementärsauerstoff zu sparen. Dosiergeräte für Sauerstoff werden üblicherweise durch einen nicht fachkundigen Bediener angewendet.
ANMERKUNG 1 Dosiergeräte können auch in gewerblichen Gesundheitseinrichtungen verwendet werden.
ANMERKUNG 2 Dosiergeräte können mit einem Sauerstoff-Konzentrator verwendet werden.
Dieses Dokument gilt auch für Zubehör, für das der Hersteller den Anschluss an einen Anfeuchter vorsieht, bei dem die Merkmale dieses Zubehörs die Basissicherheit und die wesentlichen Leistungsmerkmale des Anfeuchters beeinflussen können.
Dieses Dokument gilt nur für aktive Geräte (z. B. pneumatisch oder elektrisch betrieben), sie gilt nicht für nichtaktive Medizinprodukte (z. B. Nasenbrillen mit Reservoir).
ANMERKUNG 3 Dosiergeräte nach diesem Dokument können in andere Geräte eingebaut werden, für die es eigene Normen gibt und in diesem Fall muss die Kombination beiden Normen entsprechen.
BEISPIEL Dosiergerät kombiniert mit einem Druckminderer [Reihe (ISO 10524], einem Sauerstoff-Konzentrator [2] oder Flüssigsauerstoffgeräten [3].
Wenn ein Abschnitt oder Unterabschnitt speziell nur auf ME-Geräte oder ME-Systeme angewendet werden soll, wird dies aus der Überschrift und dem Inhalt des jeweiligen Abschnitts oder Unterabschnitts deutlich. In den übrigen Fällen gilt der Abschnitt oder Unterabschnitt je nach Zutreffen für sowohl ME-Geräte als auch ME-Systeme.
Gefährdungen, die der vorgesehenen physiologischen Funktion der in den Anwendungsbereich dieses Dokuments fallenden ME-Geräte oder ME-Systeme inhärent sind, werden nicht durch die spezifischen Anforderungen dieser Norm abgedeckt, ausgenommen sind IEC 60601-1:2005+AMD1:2012, 7.2.13 und 8.4.1.
ANMERKUNG 4 Zusätzliche Angaben können IEC 60601 1:2005+AMD1:2012, 4.2, entnommen werden.
Dieses Dokument ist eine besondere Norm aus den Normenreihen IEC 60601 und IEC/ISO 80601.
Appareils électromédicaux - Partie 2-67: Exigences particulières pour la sécurité de base et les performances essentielles dee économiseurs d'oxygène ISO 80601-2-67:2020)
Le présent document s'applique à la sécurité de base et aux performances essentielles d'un économiseur d'oxygène, désigné ci-après sous le terme d'appareil EM, ainsi que de ses accessoires prévus pour économiser le supplément d'oxygène en délivrant du gaz de manière intermittente et synchronisée en suivant le cycle d'inspiration du patient, pour une utilisation dans l'environnement de soins à domicile. L'économiseur d'oxygène est habituellement utilisé par un opérateur non spécialiste.
NOTE 1 Un économiseur peut également être utilisé dans des établissements de santé.
Le présent document s'applique également aux économiseurs intégrés à d'autres appareils.
EXEMPLE Économiseur associé à un détendeur[2], un concentrateur d'oxygène[7] ou un appareil à oxygène liquide[4].
Le présent document s'applique également aux accessoires destinés par leur fabricant à être raccordés à un économiseur, du fait que les caractéristiques de ces accessoires peuvent avoir un impact sur la sécurité de base ou sur les performances essentielles de l'économiseur.
Le présent document vise à préciser les différences de fonctionnement entre différents modèles d'économiseurs, ainsi que les différences de fonctionnement entre économiseurs et appareils à oxygène à débit continu, en exigeant des essais de performance et un étiquetage normalisés.
Le présent document ne s'applique qu'aux dispositifs actifs (par exemple, dotés d'une alimentation pneumatique ou électrique) et ne s'applique pas aux dispositifs non actifs (par exemple, canules de réservoir).
Si un article ou un paragraphe est spécifiquement destiné à être appliqué uniquement aux appareils EM ou uniquement aux systèmes EM, le titre et le contenu dudit article ou paragraphe l'indiqueront. Si cela n'est pas le cas, l'article ou le paragraphe s'applique à la fois aux appareils EM et aux systèmes EM, selon le cas.
Les dangers inhérents à la fonction physiologique prévue des appareils EM ou des systèmes EM dans le cadre du domaine d'application du présent document ne sont pas couverts par des exigences spécifiques contenues dans le présent document, à l'exception de l'IEC 60601‑1:2005+AMD1:2012, 7.2.13 et 8.4.1.
NOTE 2 Des informations supplémentaires peuvent être trouvées dans l'IEC 60601‑1:2005+AMD1:2012, 4.2.
Medicinska električna oprema - 2-67. del: Posebne zahteve za osnovno varnost in bistvene lastnosti opreme za shranjevanje kisika (ISO 80601-2-67:2020)
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 80601-2-67:2021
01-januar-2021
Nadomešča:
SIST EN ISO 18779:2005
Medicinska električna oprema - 2-67. del: Posebne zahteve za osnovno varnost in
bistvene lastnosti opreme za shranjevanje kisika (ISO 80601-2-67:2020)
Medical electrical equipment - Part 2-67: Particular requirements for basic safety and
essential performance of oxygen-conserving equipment (ISO 80601-2-67:2020)Medizinische elektrische Geräte- - Teil 2-67: Besondere Festlegungen für die
Basissicherheit einschließlich der wesentlichen Leistungsmerkmale von Sauerstoff-
Dosiergeräten ISO 80601-2-67:2020)Appareils électromédicaux - Partie 2-67: Exigences particulières pour la sécurité de base
et les performances essentielles dee économiseurs d'oxygène ISO 80601-2-67:2020)Ta slovenski standard je istoveten z: EN ISO 80601-2-67:2020
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN ISO 80601-2-67:2021 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 80601-2-67:2021
EN ISO 80601-2-67
EUROPEAN STANDARD
NORME EUROPÉENNE
November 2020
EUROPÄISCHE NORM
ICS 11.040.10 Supersedes EN ISO 18779:2005
English Version
Medical electrical equipment - Part 2-67: Particular
requirements for basic safety and essential performance of
oxygen-conserving equipment (ISO 80601-2-67:2020)
Appareils électromédicaux - Partie 2-67: Exigences Medizinische elektrische Geräte - Teil 2-67: Besondere
particulières pour la sécurité de base et les Festlegungen für die Sicherheit einschließlich der
performances essentielles des économiseurs d'oxygène wesentlichen Leistungsmerkmale von Sauerstoff-
(ISO 80601-2-67:2020) Dosiergeräten (ISO 80601-2-67:2020)This European Standard was approved by CEN on 8 October 2020.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this
European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.This European Standard exists in three official versions (English, French, German). A version in any other language made by
translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management
Centre has the same status as the official versions.CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and
United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2020 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 80601-2-67:2020 E
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SIST EN ISO 80601-2-67:2021
EN ISO 80601-2-67:2020 (E)
Contents Page
European foreword ....................................................................................................................................................... 3
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EN ISO 80601-2-67:2020 (E)
European foreword
This document (EN ISO 80601-2-67:2020) has been prepared by Technical Committee ISO/TC 121
"Anaesthetic and respiratory equipment" in collaboration with Technical Committee CEN/TC 215
“Respiratory and anaesthetic equipment” the secretariat of which is held by BSI.This European Standard shall be given the status of a national standard, either by publication of an
identical text or by endorsement, at the latest by May 2021, and conflicting national standards shall be
withdrawn at the latest by May 2021.Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 18779:2005.According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.Endorsement notice
The text of ISO 80601-2-67:2020 has been approved by CEN as EN ISO 80601-2-67:2020 without any
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SIST EN ISO 80601-2-67:2021
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SIST EN ISO 80601-2-67:2021
INTERNATIONAL ISO
STANDARD 80601-2-67
Second edition
2020-10
Medical electrical equipment —
Part 2-67:
Particular requirements for basic
safety and essential performance of
oxygen-conserving equipment
Appareils électromédicaux —
Partie 2-67: Exigences particulières pour la sécurité de base et les
performances essentielles des économiseurs d'oxygène
Reference number
ISO 80601-2-67:2020(E)
ISO 2020
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2020
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2020 – All rights reserved
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
Contents Page
Foreword ........................................................................................................................................................................... v
Introduction ................................................................................................................................................................... vi
201. 1 * Scope, object and related standards ...................................................................................................... 1
201. 2 Normative references .................................................................................................................................... 3
201. 3 Terms and definitions .................................................................................................................................... 4
201. 4 General requirements .................................................................................................................................... 5
201. 5 General requirements for testing of ME equipment ............................................................................ 7
201. 6 Classification of ME equipment and ME systems ................................................................................... 8
201. 7 * ME equipment identification, marking and documents .................................................................. 8
201. 8 Protection against electrical hazards from ME equipment ............................................................ 15
201. 9 Protection against mechanical hazards of ME equipment and ME systems .............................. 15
201. 10 Protection against unwanted and excessive radiation hazards .................................... 16
201. 11 Protection against excessive temperatures and other hazards .................................... 16
201. 12 Accuracy of controls and instruments and protection against hazardousoutputs .............................................................................................................................................................. 18
201. 13 Hazardous situations and fault conditions ............................................................................ 21
201. 14 Programmable electrical medical systems (PEMS) ............................................................. 21
201. 15 Construction of ME equipment ................................................................................................... 22
201. 16 ME systems ........................................................................................................................................ 22
201. 17 Electromagnetic compatibility of ME equipment and ME systems ................................ 22
201.101 Gas connections.......................................................................................................................................... 22
201.102 Requirements for parts and accessories ........................................................................................... 23
201.103 Oxygen pressure regulators .................................................................................................................. 25
202 Electromagnetic disturbances – Requirements and tests .............................................................. 25
202.4.3.1 * Configurations .............................................................................................................................. 25
206 Usability ........................................................................................................................................................... 26
Annex C (informative) Guide to marking and labelling requirements for ME equipment and
ME systems ....................................................................................................................................................... 27
Annex D (informative) Symbols on marking ................................................................................................... 32
Annex AA (informative) Particular guidance and rationale ...................................................................... 33
Annex BB (informative) Reference to the IMDRF essential principles and labelling
guidances ......................................................................................................................................................... 42
Annex CC (informative) Reference to the essential principles ................................................................... 46
Annex DD (informative) Reference to the general safety and performance requirements ........... 49
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
Annex EE (informative) Terminology — Alphabetized index of defined terms ................................. 53
Bibliography ................................................................................................................................................................. 56
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
Foreword
ISO (the International Organization for Standardization) and IEC (the International Electrotechnical
Commission) form the specialized system for worldwide standardization. National bodies that are
members of ISO or IEC participate in the development of International Standards through technical
committees established by the respective organization to deal with particular fields of technical activity.
ISO and IEC technical committees collaborate in fields of mutual interest. Other international
organizations, governmental and non-governmental, in liaison with ISO and IEC, also take part in the
work.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 document 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 and IEC 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) or the
IEC list of patent declarations received (see http://patents.iec.ch).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 jointly by Technical Committee ISO/TC 121, Anaesthetic and respiratory
equipment, Subcommittee SC 3, Respiratory devices and related equipment used for patient care, and
Technical Committee IEC/TC 62, Electrical equipment in medical practice, Subcommittee SC D,
Electromedical equipment, in collaboration with the European Committee for Standardization (CEN)
Technical Committee CEN/TC 215, Respiratory and anaesthetic equipment, in accordance with the
Agreement on technical cooperation between ISO and CEN (Vienna Agreement).This second edition cancels and replaces the first edition (ISO 80601-2-67:2014), which has been
technically revised.The main changes compared to the previous edition are as follows:
— clarified the accessibility of inlet and outlet connectors;
— formatted to provide a unique identifier for each requirement; and
— harmonization with the ‘A2 project’ of the general standard.
A list of all parts in the ISO and IEC 80601 series can be found on the ISO and IEC websites.
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.© ISO 2020 – All rights reserved v
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
Introduction
Long-term oxygen therapy has been demonstrated in randomized, controlled clinical trials to prolong
survival in patients with chronic respiratory disease and documented hypoxemia. Typical sources of
therapeutic long-term oxygen therapy include gaseous oxygen from cylinders or from liquid oxygen and
oxygen from an oxygen concentrator.Most clinicians prescribe low flow oxygen therapy as continuous flow oxygen (CFO) delivery in l/min.
CFO systems deliver the flow of oxygen without regard for the patient’s breathing rate or pattern.
Outside of the institutional care setting, the provision of CFO therapy is often a significant expense and
can limit the mobility of a patient to the immediate vicinity of a stationary or fixed oxygen delivery
system. To support mobility, patients use CFO from portable liquid or compressed oxygen systems with
a limited storage capacity that can limit a patient’s time and activities while away from a stationary
oxygen supply.Conserving equipment that delivers supplemental oxygen as a bolus conserves usage while allowing
satisfactory patient arterial oxygen saturation (SaO ) to be maintained during daily activities.
Conserving equipment delivers supplemental oxygen unlike CFO in that the therapy gas flow is delivered
only during the inspiratory phase of the breathing cycle, when it is most likely to reach the alveoli.
During both the expiratory and pause phase of the breathing cycle, the flow of supplemental oxygen is
stopped, minimizing waste. Because flow over time produces a volume, the bolus delivered by the
conserving equipment is typically represented as a volume of gas. Therapy using conserving equipment
versus CFO results in lower operating costs and longer ambulatory times for patients using the same
CFO storage capacity.Operation of conserving equipment from various manufacturers might differ in the dose delivery
mechanism resulting in variations in oxygen therapy to the patient. The use of CFO numerical markings
for dose settings on conserving equipment might not directly correlate with CFO settings and might lead
to misinterpretation of gas delivery rates and volumes for a particular patient. This might result in
incorrect patient setup and therapy delivery over all breathing rates and patterns versus CFO. Because
of the differences in delivery, settings, and markings versus CFO therapy, conserving equipment use has
requirements for patient titration to determine the proper setting(s) needed to provide adequate SaO
levels for the patient breathing patterns.In this document, the following print types are used:
— requirements and definitions: roman type;
— test specifications and terms defined in Clause 3 of the general standard, in this particular document
or as noted: italic type; and— informative material appearing outside of tables, such as notes, examples and references: in smaller type.
Normative text of tables is also in a smaller type.In referring to the structure of this document, the term.
— “clause” means one of the three numbered divisions within the table of contents, inclusive of all
subdivisions (e.g. Clause 201 includes subclauses 201.7, 201.8, etc.); and— “subclause” means a numbered subdivision of a clause (e.g. 201.7, 201.8 and 201.9 are all
subclauses of Clause 201).References to clauses within this document are preceded by the term “Clause” followed by the clause
number. References to subclauses within this particular document are by number only.
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
In this document, the conjunctive “or” is used as an “inclusive or” so a statement is true if any
combination of the conditions is true.For the purposes of this document, the auxiliary verb:
— “shall” means that conformance with a requirement or a test is mandatory for conformance with
this document;— "should” means that conformance with a requirement or a test is recommended but is not
mandatory for conformance with this document;— "may” is used to describe a permission (e.g., permissible way to achieve conformance with a
requirement or test;— "can" is used to describe a possibility or capability; and
— "must" is used to express an external constraint.
Annex C contains a guide to the marking and labelling requirements in this document.
Annex D contains a summary of the symbols referenced in this document.An asterisk (*) as the first character of a title or at the beginning of a paragraph or table title indicates
that there is guidance or rationale related to that item in Annex AA.© ISO 2020 – All rights reserved vii
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SIST EN ISO 80601-2-67:2021
INTERNATIONAL STANDARD ISO 80601-2-67:2020(E)
Medical electrical equipment —
Part 2-67:
Particular requirements for basic safety and essential
performance of oxygen conserving equipment
201.1 * Scope, object and related standards
IEC 60601-1:2005+AMD1:2012+AMD2:2020, Clause 1 applies, except as follows:
NOTE The general standard is IEC 60601-1:2005+AMD1:2012+AMD2:2020.
201.1.1 Scope
IEC 60601-1:2005+AMD1:2012, 1.1 is replaced by:
This document is applicable to the basic safety and essential performance of oxygen conserving
equipment, hereafter referred to as ME equipment, in combination with its accessories intended to
conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's
inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is
typically used by a lay operator.NOTE 1 Conserving equipment can also be used in professional health care facilities.
This document is also applicable to conserving equipment that is incorporated with other equipment.
[2] [7]EXAMPLE Conserving equipment combined with a pressure regulator , an oxygen concentrator or liquid
[4]oxygen equipment .
This document is also applicable to those accessories intended by their manufacturer to be connected to
conserving equipment, where the characteristics of those accessories can affect the basic safety or
essential performance of the conserving equipment.This document is intended to clarify the difference in operation of various conserving equipment
models, as well as between the operation of conserving equipment and continuous flow oxygen
equipment, by requiring standardized performance testing and labelling.This document is only applicable to active devices (e.g. pneumatically or electrically powered) and is
not applicable to non-active devices (e.g. reservoir cannulas).If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems
only, the title and content of that clause or subclause will say so. If that is not the case, the clause or
subclause applies both to ME equipment and to ME systems, as relevant.Hazards inherent in the intended physiological function of ME equipment or ME systems within the
scope of this document are not covered by specific requirements in this document except in IEC 60601-
1:2005+AMD1:2012, 7.2.13 and 8.4.1.© ISO 2020 – All rights reserved 1
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ISO 80601-2-67:2020(E)
NOTE 2 Additional information can be found in IEC 60601-1:2005+AMD1:2012, 4.2.
201.1.2 Object
IEC 60601-1:2005, 1.2 is replaced by:
The object of this document is to establish particular basic safety and essential performance
requirements for conserving equipment [as defined in 201.3.201] and its accessories.
NOTE 1 Accessories are included because accessories can have a significant impact on the basic safety or
essential performance of conserving equipment.[11] [12]
NOTE 2 This document has been prepared to address the relevant essential principles and labelling
guidances of the International Medical Devices Regulators Forum (IMDRF) as indicated in Annex BB.
NOTE 3 This document has been prepared to address the relevant essential principles of safety and performance
of ISO 16142-1:2016 as indicated in Annex CC.NOTE 4 This document has been prepared to address the relevant general safety and performance
[10]requirements of European regulation (EU) 2017/745 as indicated in Annex DD.
201.1.3 Collateral standards
IEC 60601-1:2005+AMD1:2012+AMD2:2020, 1.3 applies with the following addition:
IEC 60601-1-2+AMD1:2020 and IEC 60601-1-6+AMD1:2013+AMD2:2020 apply as modified in Clauses
202 and 206 respectively. IEC 60601-1-3:2008+AMD1:2013 does not apply. All other published
collateral standards in the IEC 60601-1 series apply as published.201.1.4 Particular standards
Replacement:
In the IEC 60601 series, particular standards define basic safety and essential performance
requirements, and may modify, replace or delete requirements contained in the general standard and
collateral standards as appropriate for the particular ME equipment under consideration.
A requirement of a particular standard takes priority over the general standard.For brevity, IEC 60601-1+AMD1:2012+AMD2:— is referred to in this document as the general standard.
Collateral standards are referred to by their document number.The numbering of clauses and subclauses of this document corresponds to that of the general standard
with the prefix “201” (e.g. 201.1 in this document addresses the content of Clause 1 of the general
standard) or applicable collateral standard with the prefix “20x”, where x is the final digit(s) of the
collateral standard document number (e.g. 202.4 in this document addresses the content of Clause 4 of
the IEC 60601-1-2 collateral standard, 206.4 in this document addresses the content of Clause 4 of the
IEC 60601-1-6 collateral standard, etc.). The changes to the text of the general standard are specified by
the use of the following words:"Replacement" means that the clause or subclause of the general standard or applicable collateral
standard is replaced completely by the text of this document.2 © ISO 2020 – All rights reserved
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ISO 80601-2-67:2020(E)
"Addition" means that the text of this document is additional to the requirements of the general
standard or applicable collateral standard."Amendment" means that the clause or subclause of the general standard or applicable collateral
standard is amended as indicated by the text of this document.Subclauses, figures or tables which are additional to those of the general standard are numbered
starting from 201.101. However, due to the fact that definitions in the general standard are numbered
3.1 through 3.147, additional definitions in this document are numbered beginning from 201.3.201.
Additional annexes are lettered AA, BB, etc., and additional items aa), bb), etc.
Subclauses, figures or tables which are additional to those of a collateral standard are numbered
starting from 20x, where “x” is the number of the collateral standard, e.g. 202 for IEC 60601-1-2, 206 for
IEC 60601-1-6, etc.The term "this document" is used to make reference to the general standard, any applicable collateral
standards and this particular document taken together.Where there is no corresponding clause or subclause in this document, the clause or subclause of the
general standard or applicable collateral standard, although possibly not relevant, applies without
modification; where it is intended that any part of the general standard or applicable collateral
standard, although possibly relevant, is not to be applied, a statement to that effect is given in this
document.201.2 Normative references
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments) applies.
IEC 60601-1:2005+AMD1:2012+AMD2:2020, Clause 2 applies, except as follows:Replacement:
ISO 15223-1:— , Medical devices — Symbols to be used with medical device labels, labelling and
information to be supplied — Part 1: General requirementsAddition:
ISO 32:1977, Gas cylinders for medical use — Marking for identification of content
ISO 5359:2014+Amd.1:2017, Low-pressure hose assemblies for use with medical gases
ISO 7000, Graphical symbols for use on equipment — Registered symbolsISO 7396-1:2016, Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases
and vacuumISO 9000:2015, Quality management systems — Fundamentals and vocabulary
Under preparation. Stage at the time of publication: ISO/DIS 15223-1:2020.
© ISO 2020 – All rights reserved 3
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SIST EN ISO 80601-2-67:2021
ISO 80601-2-67:2020(E)
ISO 10524-1:2018, Pressure regulators for use with medical gases — Part 1: Pressure regulators and
pressure regulators with flow-metering devicesISO 10524-3:2019, Pressure regulators for use with medical gases — Part 3: Pressure regulators
integrated with cylinder valves (VIPRs)ISO 14937:2009, Sterilization of health care products — General requirements for characterization of a
sterilizing agent and the development, validation and routine control of a sterilization process for medical
devicesISO 16142-1:2016, Medical devices — Recognized essential principles of safety and performance of
medical devices — Part 1: General essential principles and additional specific essential principles for all
non-IVD medical devices and guidance on the selection of standardsISO 17664:2017, Processing of health care products — Information to be provided by the medical device
manufacturer for the processing of medical devicesISO 18562-1:2017, Biocompatibility evaluation of breathing gas pathways in healthcare applications —
Part 1: Evaluation and testing within a risk management processISO 19223:2019, Lung ventilators and related equipment — Vocabulary and semantics
ISO 80369-1:2018, Small-bore connectors for liquids and gases in healthcare applications — Part 1:
General requirementsISO 80601-2-74:2017, Medical electrical equipment — Part 2-74: Particular requirements for basic safety
and essential performance of respiratory humidifying e...
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