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SLOVENSKI STANDARD
01-junij-2022
Infuzijska oprema za uporabo v medicini - 15. del: Infuzijski seti za enkratno
uporabo, zaščiteni pred svetlobo (ISO 8536-15:2022)
Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use
(ISO 8536-15:2022)
Infusionsgeräte zur medizinischen Verwendung - Teil 15: Lichtbeständige
Infusionsgeräte zur einmaligen Verwendung (ISO 8536-15:2022)
Matériel de perfusion à usage médical - Partie 15: Perfuseurs photoprotecteurs à usage
unique (ISO 8536-15:2022)
Ta slovenski standard je istoveten z: EN ISO 8536-15:2022
ICS:
11.040.20 Transfuzijska, infuzijska in Transfusion, infusion and
injekcijska oprema injection equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
EN ISO 8536-15
EUROPEAN STANDARD
NORME EUROPÉENNE
March 2022
EUROPÄISCHE NORM
ICS 11.040.20
English Version
Infusion equipment for medical use - Part 15: Light-
protective infusion sets for single use (ISO 8536-15:2022)
Matériel de perfusion à usage médical - Partie 15: Infusionsgeräte zur medizinischen Verwendung - Teil
Perfuseurs photoprotecteurs à usage unique (ISO 15: Lichtbeständige Infusionsgeräte zur einmaligen
8536-15:2022) Verwendung (ISO 8536-15:2022)
This European Standard was approved by CEN on 21 February 2022.
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
© 2022 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8536-15:2022 E
worldwide for CEN national Members.
Contents Page
European foreword . 3
European foreword
This document (EN ISO 8536-15:2022) has been prepared by Technical Committee ISO/TC 76
"Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical
use" in collaboration with Technical Committee CEN/TC 205 “Non-active medical devices” the
secretariat of which is held by DIN.
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 September 2022, and conflicting national standards
shall be withdrawn at the latest by September 2022.
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.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
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 8536-15:2022 has been approved by CEN as EN ISO 8536-15:2022 without any
modification.
INTERNATIONAL ISO
STANDARD 8536-15
First edition
2022-03
Infusion equipment for medical use —
Part 15:
Light-protective infusion sets for
single use
Matériel de perfusion à usage médical —
Partie 15: Perfuseurs photoprotecteurs à usage unique
Reference number
ISO 8536-15:2022(E)
ISO 8536-15:2022(E)
© ISO 2022
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: [email protected]
Website: www.iso.org
Published in Switzerland
ii
ISO 8536-15:2022(E)
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 General requirements . 1
5 Materials . 1
6 Physical requirements . 2
6.1 General . 2
6.2 Transparency . 2
6.3 Light-protective performance . . . 2
6.4 Decolourization . 2
7 Chemical requirements . 2
8 Biological requirements . 2
9 Labelling . 3
10 Packaging. 3
11 Disposal . 3
Annex A (normative) Determination of light transmittance . 4
Annex B (normative) Decolourization test – physical method . 6
Annex C (normative) Chemical method for decolourization test – visual colorimetry .7
Bibliography . 8
iii
ISO 8536-15:2022(E)
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 Technical Committee ISO/TC 76, Transfusion, infusion and injection,
and blood processing equipment for medical and pharmaceutical use, in collaboration with the European
Committee for Standardization (CEN) Technical Committee CEN/TC 205, Non-active medical devices, in
accordance with the Agreement on technical cooperation between ISO and CEN (Vienna Agreement).
A list of all parts in the ISO 8536 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.
iv
ISO 8536-15:2022(E)
Introduction
With the continuous development of infusion technology and the increasingly exacting clinical
requirements, some infusion sets need to be adapted to specific clinical requirements.
Some pharmaceuticals, such as sodium nitroprusside, nitroglycerin and vitamin B2, are light sensitive
and need to be clinically infused under light-protective conditions; this document is applicable to such
sets.
This document stipulates the light-transmission requirements for the drip chamber and the tube. Since
other components are limited by their external dimensions, they are not subject to light-transmission
requirements and whether they will be light-protective or not is at the manufacturer’s discretion.
It is the responsibility of the device manufacturer to keep the light-protection of the infusion sets stable
during the shelf life. Annex A, Annex B and Annex C give the methods for evaluation of light-protective
infusion sets.
v
INTERNATIONAL STANDARD ISO 8536-15:2022(E)
Infusion equipment for medical use —
Part 15:
Light-protective infusion sets for single use
1 Scope
This document specifies the requirements for infusion sets for single use that use light-protective
agents in the fluid p
...