EN 28362-3:1993
(Main)Injection containers for injectables and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:1989)
Injection containers for injectables and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:1989)
Injektionsbehältnisse für Injektionspräparate und Zubehör - Teil 3: Aluminium-Bördelkappen für Injektionsflaschen (ISO 8362-3:1989)
Récipients et accessoires pour produits injectables - Partie 3: Capsules en aluminium pour flacons (ISO 8362-3:1989)
Vsebniki za parenteralne farmacevtske oblike in dodatna oprema - 3. del: Aluminijeve zaporke za viale (ISO 8362-3:1989)
General Information
Relations
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Vsebniki za parenteralne farmacevtske oblike in dodatna oprema - 3. del: Aluminijeve zaporke za viale
(ISO 8362-3:1989)Injektionsbehältnisse für Injektionspräparate und Zubehör - Teil 3: Aluminium-Bördelkappen für Injektionsflaschen (ISO 8362-3:1989)Récipients et accessoires pour produits injectables - Partie 3: Capsules en aluminium pour flacons (ISO 8362-3:1989)Injection containers for injectables and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:1989)11.040.20Transfuzijska, infuzijska in injekcijska opremaTransfusion, infusion and injection equipmentICS:Ta slovenski standard je istoveten z:EN 28362-3:1993SIST EN 28362-3:2000en01-januar-2000SIST EN 28362-3:2000SLOVENSKI
STANDARD
SIST EN 28362-3:2000
SIST EN 28362-3:2000
SIST EN 28362-3:2000
SIST EN 28362-3:2000
SIST EN 28362-3:2000
INTERNATIONAL STANDARD ISO 8362-3 First editisn 1989-11-15 Injection Containers for injectables and accessories - Part 3 : Aluminium taps for injection vials Rkipients et accessoires pour produits injec tables - Partie 3 : Capsules en aluminium pour flacons Reference number ISO 8362-3 : 1989 (El SIST EN 28362-3:2000
ISO 8362-3 : 1989 (EI Contents Foreword . iii Introduction . iv 1 Scope . 1 2 Normative reference . 1 3 Dimensions and designation . 1 4 Requirements . 3 5 Packaging . 3 6 Marking . 3 0 ISO 1989 All rights reserved. NO part of this publication may be reproduced or utilized in any ferm or by any means, electronie or mechanical, including photocopying and microfilm, without permission in writing from the publisher. International Organization for Standardization Case postale 56 l CH-1211 Geneve 20 l Switzerland Printed in Switzerland SIST EN 28362-3:2000
ISO 8362-3 : 1989 (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. Esch 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, govern- mental 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. Draft International Standards adopted by the technical committees are circulated to the member bodies for approval before their acceptance as International Standards by the ISO Council. They are approved in accordance with ISO procedures requiring at least 75 % approval by the member bodies voting. International Standard ISO 8361-3 was prepared by Technical Committee ISO/TC 76, Transfusion, infusion and injection equipmen t for medical use. ISO 8362 consists of the following Parts, under the general title lnjection Containers for injectables and accessories : - Part 7: lnjection vials made of glass tubing - Part 2 : Closures for injection vials - Part 3 : Aluminium taps for injection vials - Part 4: lnjection vials made of moulded glass SIST EN 28362-3:2000
ISO 8362-3 : 1989 (EI Introduction The materials from which injection Containers (including the elastomeric closures) are made are suitable primary packaging materials for storing injectable products until they are administered. However, in this pa
...
Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.