Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps - Amendment 1: Connectors

Implants cardiovasculaires et systèmes extracorporels — Systèmes de pontage cardiopulmonaire — Pièges à bulles veineuses — Amendement 1: Raccords

General Information

Status
Published
Publication Date
17-Dec-2019
Current Stage
6060 - International Standard published
Start Date
18-Dec-2019
Due Date
04-Oct-2020
Completion Date
18-Dec-2019

Relations

Effective Date
01-Jan-2022

Overview

ISO 18241:2016/Amd 1:2019 is an important amendment to the international standard for cardiovascular implants and extracorporeal systems, specifically addressing cardiopulmonary bypass systems and venous bubble traps. Released by the International Organization for Standardization (ISO), this amendment focuses on connectors used in these medical devices, ensuring secure and standardized connections between blood pathway components.

The amendment guides manufacturers, healthcare providers, and regulatory bodies on connector specifications, testing, and compatibility. It incorporates references to ISO 80369-7, which standardizes small-bore connectors for healthcare applications, thus enhancing patient safety by minimizing misconnections in cardiovascular procedures.

Key Topics

  • Connector Standards and Compatibility
    Connectors for venous bubble traps must ensure secure connections per testing procedures defined in the amendment. Accepted connector types include those compliant with ISO 8637-1:2017 and ISO 80369-7. The amendment also endorses connector dimensions formerly outlined by ISO 594-1 and ISO 594-2.

  • Performance Testing Requirements
    Connector performance must be validated according to ISO 80369-7, Clause 6, using reference fittings specified in Annex A. These tests verify mechanical strength, secure locking, and resistance to accidental disconnection.

  • Luer and Luer Lock Fittings
    Detailed in Annex A, the amendment illustrates and specifies dimensions for 6% (Luer) conical slip fittings and Luer lock fittings. These connectors are widely used to connect tubing in cardiopulmonary bypass systems, ensuring leak-proof and secure joints.

  • Gauging and Reference Fittings
    Standardized steel gauges and reference fittings described in the annex help manufacturers maintain product conformity during quality control and certification processes. These tools ensure fittings meet dimensional and mechanical requirements to prevent clinical failures.

Applications

ISO 18241:2016/Amd 1:2019 serves critical applications in the medical device industry including:

  • Cardiopulmonary Bypass Systems
    Ensuring reliable venous bubble trap connections enhances patient safety during heart surgeries by preventing air embolism.

  • Extracorporeal Circulation Devices
    Connectors that comply with this amendment support safe blood flow management outside the body, including during dialysis and cardiac support.

  • Medical Device Design and Manufacturing
    Manufacturers use the amendment to design connectors with consistent dimensions and performance characteristics facilitating global regulatory acceptance.

  • Clinical Risk Management
    Standardized connectors reduce risks of misconnections and compatibility errors, contributing to better outcomes and compliance with healthcare safety protocols.

Related Standards

  • ISO 80369-7:2016
    Specifies small-bore connectors for intravascular or hypodermic applications, referenced by ISO 18241 Amendment 1 to harmonize connector safety.

  • ISO 8637-1:2017
    Pertains to extracorporeal blood purification devices with related connector specifications that complement cardiopulmonary bypass system requirements.

  • ISO 594-1 & ISO 594-2 (Superseded)
    Former standards for conical fittings referenced for dimensional legacy compatibility within Annex A.

Summary

ISO 18241:2016/Amd 1:2019 standardizes connectors for venous bubble traps in cardiopulmonary bypass systems, ensuring secure, reliable, and safe blood pathway connections. By aligning with ISO 80369-7 and providing detailed dimensional guidelines, it supports the manufacture and use of connectors that minimize clinical risks and improve device interoperability. This amendment plays a pivotal role in advancing cardiovascular implant safety and effective extracorporeal circulation management worldwide.

Standard

ISO 18241:2016/Amd 1:2019 - Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps — Amendment 1: Connectors Released:12/18/2019

English language
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Frequently Asked Questions

ISO 18241:2016/Amd 1:2019 is a standard published by the International Organization for Standardization (ISO). Its full title is "Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps - Amendment 1: Connectors". This standard covers: Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps - Amendment 1: Connectors

Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps - Amendment 1: Connectors

ISO 18241:2016/Amd 1:2019 is classified under the following ICS (International Classification for Standards) categories: 11.040.40 - Implants for surgery, prosthetics and orthotics. The ICS classification helps identify the subject area and facilitates finding related standards.

ISO 18241:2016/Amd 1:2019 has the following relationships with other standards: It is inter standard links to ISO 18241:2016. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

ISO 18241:2016/Amd 1:2019 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)


INTERNATIONAL ISO
STANDARD 18241
First edition
2016-08-15
AMENDMENT 1
2019-12
Cardiovascular implants and
extracorporeal systems —
Cardiopulmonary bypass systems —
Venous bubble traps
AMENDMENT 1: Connectors
Implants cardiovasculaires et systèmes extracorporels — Systèmes de
pontage cardiopulmonaire — Pièges à bulles veineuses
AMENDEMENT 1: Raccords.
Reference number
ISO 18241:2016/Amd.1:2019(E)
©
ISO 2019
ISO 18241:2016/Amd.1:2019(E)
© ISO 2019
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
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Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2019 – All rights reserved

ISO 18241:2016/Amd.1:2019(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 150, Implants for surgery, Subcommittee
SC 2, Cardiovascular implants and extracorporeal systems.
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 18241:2016/Amd.1:2019(E)
Cardiovascular implants and extracorporeal systems —
Cardiopulmonary bypass systems — Venous bubble traps
AMENDMENT 1: Connectors
Clause 2
Add:
ISO 80369-7, Small-bore connectors for liquids and gases in healthcare applications — Part 7: Connectors
for intravascular or hypodermic applications
4.2.3 Connectors
Replace the text with the following:
Connectors for connection to the blood pathway shall, when tested in accordance with 5.3.3, allow a
secure connection.
NOTE 1 Connectors of a type that allows connection of tubes with an inner diameter of 4,8 mm, 6,3 mm, 9,5 mm
or 12,7 mm, or a type that complies with ISO 8637-1:2017, Figure 1, or a type that complies with ISO 80369-7 have
been found satisfactory.
NOTE 2 Connectors with dimensions as given in Annex A (formerly defined by ISO 594-1 and ISO 594-2) and
fitting to functional gauges and reference steel fittings is a way to be in accordance with this requirement.
Performance testing of the connectors shall be performed according to ISO 80369-7, Clause 6, using the
reference fittings given in Annex A.
Annex A
Add the following annex before the Bibliography:
ISO 18241:2016/Amd.1:2019(E)
Annex A
(informative)
Examples of connectors
A.1 Luer slip fittings
A.1.1 Figures A.1 and A.2 depict Luer slip fittings. For corresponding dimensions, see Table A.1.
a) Male 6 % (Luer) conical fitting (“male fitting”)
b) Female 6 % (Luer) conical fitting (“female fitting”)
NOTE See Key and dimensions in Table A.1.
Figure A.1 — Typical 6 % (Luer) conical fittings
NOTE See Key and dimensions in Table A.1.
Figure A.2 — Typical assembly of 6 % (Luer) conical fittings
2 © ISO 2019 – All rights reserved

ISO 18241:2016/Amd.1:2019(E)
Table A.1 — Dimensions of 6 % (Luer) conical fittings
Dimensions, in mm
Reference Designation
Rigid Semi-rigid
material material
A Male fitting N/A N/A
B Female fitting N/A N/A
Basic Minimum diameter of the end of the male conical fitting
min. 3,925 3,925
dimensions (reference diameter)
d
max. Maximum diameter at the end of the male conical fitting 3,990 4,027
min. Minimum diameter at the opening of the female conical fitting 4,270 4,270
D
Maximum diameter at the opening of the female conical
max. 4,315 4,315
fitting
E Minimum length of the male conical fitting 7,500 7,500
F Minimum depth of the female conical fitting 7,500 7,500
a
Other L Minimum length of engagement 4,665 4,050
dimensions
Tolerance for length of engagement of the female
a
M 0,750 0,750
conical fitting
Tolerance for length of engagement of the male
a
N 1,083 1,700
conical fitting
b
R Radius of curvature (maximum) 0,5 0,5
a
Dimensions L, M and N are derived from the basic dimensions.
b
Or equivalent entry chamfer without any sharp corners.
A.1.2 Gauging test
A.1.2.1 When tested in accordance with A.1.2.4, the conical fitting should satisfy the requirements
specified in A.1.2.2 and A.1.2.3.
A.1.2.2 The small end of the male conical fitting should lie between the two limit planes of the gauge
and the larger end of the tapered portion should extend beyond the datum plane of the gauge. Rocking
should not be evident between the gauge and the fitting made of rigid material undergoing test.
A.1.2.3 The plane of the maxim
...

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