ISO 8536-12:2007/Amd 1:2012

Infusion equipment for medical use — Part 12: Check valves — Amendment 1

Matériel de perfusion à usage médical — Partie 12: Clapet antiretour — Amendement 1

General Information

• Status: Withdrawn
• Publication Date: 30-Sep-2012
• Withdrawal Date: 30-Sep-2012
• ICS: 11.040.20 - Transfusion, infusion and injection equipment
• Technical Committee: ISO/TC 76 - Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use
• Drafting Committee: ISO/TC 76/WG 1 - Soft containers for blood, blood components and parenterals; Infusion, transfusion and blood processing equipment
• Current Stage: 9599 - Withdrawal of International Standard
• Completion Date: 04-Feb-2021

Relations

• Revised: ISO 8536-12:2021 - Infusion equipment for medical use — Part 12: Check valves for single use
• Effective Date: 31-Jul-2021
• Amends: ISO 8536-12:2007 - Infusion equipment for medical use — Part 12: Check valves
• Effective Date: 06-Jun-2022

Standards Content (Sample)

INTERNATIONAL ISO
STANDARD 8536-12
First edition
2007-04-01
AMENDMENT 1
2012-10-01
Infusion equipment for medical use —
Part 12:
Check valves
AMENDMENT 1
Matériel de perfusion à usage médical —
Partie 12: Clapet antiretour
AMENDEMENT 1
Reference number
ISO 8536-12:2007/Amd.1:2012(E)
©
ISO 2012

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ISO 8536-12:2007/Amd.1:2012(E)
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ii © ISO 2012 – All rights reserved

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ISO 8536-12:2007/Amd.1:2012(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.
International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
The main task of technical committees is to prepare International Standards. 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.
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.
Amendment 1 to ISO 8536-12:2007 was prepared by Technical Committee ISO/TC 76, Transfusion,
infusion and injection, and blood processing equipment for medical and pharmaceutical use.
© ISO 2012 – All rights reserved iii

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ISO 8536-12:2007/Amd.1:2012(E)
Infusion equipment for medical use —
Part 12:
Check valves
AMENDMENT 1
Page 1, Clause 2
Replace the last entry, ISO 15223:2000,
...