EN ISO 10555-1:1996/A1:1999
(Amendment)Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1996/AM1:1999)
Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1996/AM1:1999)
To amend EN ISO 10555-1 so as to include requirements for hydratable catheters.
Sterile intravaskuläre Katheter zur einmaligen Verwendung - Teil 1: Allgemeine Anforderungen (ISO 10555-1:1996/AM1:1999)
Cathéters intravasculaires stériles, non réutilisables - Partie 1: Prescriptions générales (ISO 10555-1:1996/AM1:1999)
Sterilni žilni katetri za enkratno uporabo - 1. del: Splošne zahteve (ISO 10555-1:1996/AM1:1999)
General Information
- Status
- Withdrawn
- Publication Date
- 14-Jul-1999
- Withdrawal Date
- 12-May-2009
- Technical Committee
- CEN/TC 205 - Non-active medical devices
- Drafting Committee
- CEN/TC 205/WG 6 - Catheters and enteral feeding tubes
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 13-May-2009
- Completion Date
- 13-May-2009
- Directive
- 93/42/EEC - Medical devices
Relations
- Effective Date
- 20-May-2009
- Effective Date
- 08-Jun-2022
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Frequently Asked Questions
EN ISO 10555-1:1996/A1:1999 is a amendment published by the European Committee for Standardization (CEN). Its full title is "Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1996/AM1:1999)". This standard covers: To amend EN ISO 10555-1 so as to include requirements for hydratable catheters.
To amend EN ISO 10555-1 so as to include requirements for hydratable catheters.
EN ISO 10555-1:1996/A1:1999 is classified under the following ICS (International Classification for Standards) categories: 11.040.20 - Transfusion, infusion and injection equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN ISO 10555-1:1996/A1:1999 has the following relationships with other standards: It is inter standard links to EN ISO 10555-1:2009, EN ISO 10555-1:1996. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN ISO 10555-1:1996/A1:1999 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
EN ISO 10555-1:1996/A1:1999 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
SLOVENSKI STANDARD
01-julij-2000
Sterilni žilni katetri za enkratno uporabo - 1. del: Splošne zahteve (ISO 10555-
1:1996/AM1:1999)
Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-
1:1996/AM1:1999)
Sterile intravaskuläre Katheter zur einmaligen Verwendung - Teil 1: Allgemeine
Anforderungen (ISO 10555-1:1996/AM1:1999)
Cathéters intravasculaires stériles, non réutilisables - Partie 1: Prescriptions générales
(ISO 10555-1:1996/AM1:1999)
Ta slovenski standard je istoveten z: EN ISO 10555-1:1996/A1:1999
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.
ISO
INTERNATIONAL
10555-1
STANDARD
First edition
1995-06-15
Amendment 1
1999-07-15
Sterile, single-use intravascular
catheters —
Part 1:
General requirements
AMENDMENT 1
Cathéters intravasculaires stériles, non réutilisables —
Partie 1: Prescriptions générales
AMENDEMENT 1
A
Reference number
ISO 10555-1:1995/Amd.1:1999(E)
ISO 10555-1:1995/Amd.1:1999(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.
Draft International Standards adopted by the technical committees are circulated to the member bodies for voting.
Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote.
Amendment 1 to International Standard ISO 10555-1 was prepared by Technical Committee ISO/TC 84, Medical
devices for injections, Subcommittee SC 1, Syringes, needles and intravascular catheters for single use.
The purpose of this amendment is to add to ISO 10555-1 general requirements for hydratable catheters.
© ISO 1999
All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic
or mechanical, including photocopying and microfilm, without permission in writing from the publisher.
International Organization for Standardization
Case postale 56 • CH-1211 Genève 20 • Switzerland
Internet iso@iso.ch
Printed in Switzerland
ii
© ISO
ISO 10555-1:1995/Amd.1:1999(E)
Sterile, single-use intravascular catheters —
Part 1:
General requirements
AMENDMENT 1
Page 1
Clause 3 Definitions
Delete existing definitions for 3.5 and 3.6, and substitute the following definitions:
3.5 effective length, l: Length of the catheter, or pre- and post-hydration lengths of hydratable catheters, that
can be inserted into the body (see figure 1).
3.6 outside diameter: Maximum diameter o
...




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