Sterile single-use syringes, with or without needle, for insulin (ISO 8537:2016)

ISO 8537:2016 specifies requirements and test methods for empty, sterile, single-use syringes, with or without needles, made of plastic materials and intended solely for the injection of insulin, with which the syringes are filled by the end user. This International Standard covers syringes intended for single-use only in humans and with insulins of various concentrations.
The insulin syringes specified in this International Standard are intended for use (i.e. insulin injection) immediately after filling and are not intended to contain insulin for extended periods of time.
ISO 8537:2016 excludes single-use syringes made of glass, syringes for use with power-driven syringe pumps, syringes that are pre-filled by the manufacturer, and syringes intended to be stored after filling (e.g. in a kit intended for filling by a pharmacist).

Sterile Insulin-Einmalspritzen mit oder ohne Kanüle (ISO 8537:2016)

Diese Internationale Norm legt Anforderungen an und Prüfverfahren für leere, sterile Einmalspritzen mit oder ohne Kanüle fest, die aus Kunststoffmaterialien hergestellt und ausschließlich zur Injektion von Insulin vorgesehen sind, mit dem die Spritzen vom Endverbraucher befüllt werden. Diese Internationale Norm gilt für Einmalspritzen, die für die Anwendung am Menschen und für verschiedene Insulinkonzentrationen vorgesehen sind.
Die in dieser Internationalen Norm festgelegten Insulinspritzen sind zum unverzüglichen Gebrauch (d. h. Insulininjektion) nach dem Befüllen bestimmt und sind nicht dafür vorgesehen, Insulin über eine längere Zeitdauer aufzubewahren.
Diese Norm gilt nicht für Einmalspritzen aus Glas, Spritzen zur Verwendung mit Spritzenpumpen, vom Hersteller vorgefüllte Spritzen und Spritzen, die für eine Lagerung nach dem Befüllen vorgesehen sind (z. B. in einem Satz, der zum Befüllen durch einen Apotheker bestimmt ist).

Seringues à insuline, stériles, non réutilisables, avec ou sans aiguille (ISO 8537:2016)

ISO 8537:2016 spécifie des exigences et des méthodes d'essai applicables aux seringues stériles vides non réutilisables, avec ou sans aiguille, constituées de plastique et uniquement destinées à l'injection d'insuline, avec laquelle les seringues sont remplies par l'utilisateur final. La présente Norme internationale concerne les seringues non réutilisables utilisées uniquement chez l'être humain et remplies d'insuline en concentrations variables.
Les seringues à insuline décrites dans la présente Norme internationale sont prévues pour être utilisées (par exemple, injection d'insuline) immédiatement après leur remplissage et ne sont pas adaptées pour contenir de l'insuline pendant de longues périodes.
ISO 8537:2016 exclut les seringues non réutilisables en verre, les seringues utilisables avec les pousse-seringues électriques, les seringues pré-remplies par le fabricant et les seringues prévues pour être conservées après leur remplissage (par exemple, dans un kit prévu pour être rempli par un pharmacien).

Sterilne injekcijske brizge za insulin za enkratno uporabo, z iglo ali brez nje (ISO 8537:2016)

Ta mednarodni standard določa zahteve in preskusne metode za prazne, sterilne
injekcijske brizge za enkratno uporabo, z iglo ali brez nje, ki so izdelane iz plastike in namenjene zgolj za vbrizganje
inzulina, pri čemer injekcije napolni končni uporabnik. Ta mednarodni standard zajema injekcijske brizge, ki so namenjene za enkratno uporabo samo pri ljudeh, z inzulinom v različnih koncentracijah.
Injekcijske brizge za inzulin, ki so določene v tem mednarodnem standardu, so namenjene za uporabo (tj. injekcija inzulina) takoj po polnjenju in ne smejo vsebovati inzulina dlje časa.
V tem mednarodnem standardu niso zajete injekcijske brizge za enkratno uporabo, izdelane iz stekla, injekcijske brizge za uporabo z injekcijskimi črpalkami, injekcijske brizge, ki jih predhodno napolni proizvajalec, in injekcijske brizge, ki so namenjene za shranjevanje po polnjenju (npr. v kompletu, ki ga napolni farmacevt).

General Information

Status
Published
Publication Date
12-Apr-2016
Withdrawal Date
30-Oct-2016
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
13-Apr-2016
Completion Date
13-Apr-2016

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SLOVENSKI STANDARD
01-junij-2016
Sterilne injekcijske brizge za insulin za enkratno uporabo, z iglo ali brez nje (ISO
8537:2016)
Sterile single-use syringes, with or without needle, for insulin (ISO 8537:2016)
Sterile Insulin-Einmalspritzen mit oder ohne Kanüle (ISO 8537:2016)
Seringues à insuline, stériles, non réutilisables, avec ou sans aiguille (ISO 8537:2016)
Ta slovenski standard je istoveten z: EN ISO 8537:2016
ICS:
11.040.25 Injekcijske brizge, igle in Syringes, needles an
katetri catheters
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EN ISO 8537
EUROPEAN STANDARD
NORME EUROPÉENNE
April 2016
EUROPÄISCHE NORM
ICS 11.040.20 Supersedes EN ISO 8537:2008
English Version
Sterile single-use syringes, with or without needle, for
insulin (ISO 8537:2016)
Seringues à insuline, stériles, non réutilisables, avec ou Sterile Insulin-Einmalspritzen mit oder ohne Kanüle
sans aiguille (ISO 8537:2016) (ISO 8537:2016)
This European Standard was approved by CEN on 27 February 2016.

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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, 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: Avenue Marnix 17, B-1000 Brussels
© 2016 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8537:2016 E
worldwide for CEN national Members.

Contents Page
European foreword . 3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC amended by Directive 2007/47/EEC . 5
European foreword
This document (EN ISO 8537:2016) has been prepared by Technical Committee ISO/TC 84 "Devices for
administration of medicinal products and catheters" 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 October 2016, and conflicting national standards shall
be withdrawn at the latest by October 2016.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent
rights.
This document supersedes EN ISO 8537:2008.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requirements of EU Directive(s).
For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this
document.
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, Former Yugoslav Republic of Macedonia, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands,
Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.
The following referenced documents are indispensable for the application of this document.
For undated references, the latest edition of the referenced document (including any amendments)
applies. For dated references, only the edition cited applies. However, for any use of this standard
‘within the meaning of Annex ZA’, the user should always check that any referenced document has not
been superseded and that its relevant contents can still be considered the generally acknowledged
state-of-art.
When an IEC or ISO standard is referred to in the ISO standard text, this shall be understood as a
normative reference to the corresponding EN standard, if available, and otherwise to the dated version
of the ISO or IEC standard, as listed below.
NOTE The way in which these referenced documents are cited in normative requirements determines the
extent (in whole or in part) to which they apply.
Table — Correlation between normative references and dated EN and ISO standards
Normative references Equivalent dated standard
as listed in Clause 2 of the ISO
EN ISO or IEC
standard
ISO 594-1 EN ISO 594-1:1986 ISO 594-1:1986
ISO 7864 EN ISO 7864:1995* ISO 7864:1993*
ISO 9626 EN ISO 9626:1995* ISO 9626:1991*
ISO 14971 EN ISO 14971:2012 ISO 14971
ISO 62366-1 EN ISO 62366-1:2015 IEC 62366-1:2015
ISO 15223-1 EN ISO 15223-1:2012 ISO 15223-1:2012
ISO 10993-1 EN ISO 10993-1:2009 ISO 10993-1:2003
ISO 80369-7 EN ISO 80369-7:2016** ISO 80369-7:2016**
* New versions expected end of 2015.
** Expected 2016.
Endorsement notice
The text of ISO 8537:2016 has been approved by CEN as EN ISO 8537:2016 without any modification.
Annex ZA
(informative)
Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC amended by Directive
2007/47/EEC
This European Standard has been prepared under a mandate given to CEN by the European
Commission and the European Free Trade Association to provide a means of conforming to the
Essential Requirements of Directive 93/42/EEC.
Once this standard is cited in the Official Journal of the European Union under that Directive and has
been implemented as a national standard in at least one Member State, compliance with the normative
clauses of this standard given in Table ZA.1 confers, within the limits of the scope of this standard, a
presumption of conformity with the corresponding Essential Requirements of that Directive and
associated EFTA Regulations.
NOTE 1 Where a reference from a clause of this standard to the risk management process is made, the risk
management process needs to be in compliance with Directive 93/42/EEC as amended by 2007/47/EC. This
means that risks have to be reduced ‘as far as possible’, ‘to a minimum’, ‘to the lowest possible level’, ‘minimized’
or ‘removed’, according to the wording of the corresponding essential requirement.
NOTE 2 The manufacturer’s policy for determining acceptable risk must be in compliance with essential
requirements 1, 2, 5, 6, 7, 8, 9, 11 and 12 of the Directive.
NOTE 3 This Annex ZA is based on normative references according to the table of references in the European
foreword, replacing the references in the core text.
NOTE 4 When an Essential Requirement does not appear in Table ZA.1, it means that it is not addressed by this
European Standard.
Table ZA.1 — Correspondence between this European Standard and Directive 93/42/EEC
Essential
Clause(s)/subclause(s) of this Requirements (ERs)
Qualifying remarks/notes
European Standard of Directive
93/42/EEC
5.1 m 7.1
6.1.2 c, 6.1.3 c, 6.2 b 7.2
5.2, 5.4 7.3
5.11.2, 5.11.3 7.5
6.1 7.6
6.1.2, 6.1.3, 7.2.2, 7.3, 7.4 8.3
5.1 n 8.4
5.1, 5.4, 5.6, 5.7, 7.3 g, 7.4 h, 7.5 h, 7.6 f 9.2
5.1 e, 5.1 g 10.1
5.1 e, 5.2 10.2
5.1 f 10.3
Clause 7 13.1
Clause 7 13.2
7.2.1, 7.2.2, 7.3, 7.4, 7.5, 7.6, 7.7 13.3
7.2.1 b, 7.3 e, 7.4 g 13.4
13.6 The information is provided on
7.4, 7.5, 7.6 the packaging and no additional
instruction for use is required
WARNING — Other requirements and other EU Directives may be applicable to the product(s) falling
within the scope of this standard.
INTERNATIONAL ISO
STANDARD 8537
Third edition
2016-03-15
Sterile single-use syringes, with or
without needle, for insulin
Seringues à insuline, stériles, non réutilisables, avec ou sans aiguille
Reference number
ISO 8537:2016(E)
©
ISO 2016
ISO 8537:2016(E)
© ISO 2016, Published in Switzerland
All rights reserved. Unless otherwise specified, 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.
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ii © ISO 2016 – All rights reserved

ISO 8537:2016(E)
Contents Page
Foreword .v
Introduction .vi
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 2
4 Types of syringes . 5
5 Requirements . 5
5.1 General requirements . 5
5.2 Material selection . 6
5.3 Colour coding . 6
5.4 Extraneous matter . 7
5.4.1 General. 7
5.4.2 Limits for acidity or alkalinity . 7
5.4.3 Limits for extractable metals. 7
5.5 Lubrication . 7
5.5.1 Lubrication of syringes . 7
5.5.2 Lubrication of needle tube . 8
5.6 Dimensions . 8
5.6.1 Barrel and plunger stopper . 8
5.6.2 Finger grips . 8
5.7 Plunger/plunger stopper . 8
5.7.1 General.
...

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