Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2009 + Amd 1:2012)

EN ISO 7199 + A1 specifies requirements for sterile, single-use, extracorporeal blood-gas exchangers (oxygenators) intended for supply of oxygen to, and removal of carbon dioxide from, the blood of humans.

Kardiovaskuläre Implantate und künstliche Organe - Blutgasaustauscher (Oxygenatoren) (ISO 7199:2009 + Amd 1:2012)

Diese Internationale Norm legt Anforderungen an sterile extrakorporale Blutgasaustauscher (Oxygenatoren) zum Einmalgebrauch fest, die zur Zufuhr von Sauerstoff in das und zur Entfernung von Kohlendioxid aus dem menschliche(n) Blut bestimmt sind.
Diese Internationale Norm gilt auch für Wärmeaustauscher, die in Oxygenatoren integriert sind, und für Außengeräte, die allein für den Gebrauch mit dem Gerät bestimmt sind.
Diese Internationale Norm gilt nicht für:
-   implantierte Oxygenatoren;
-   Flüssigkeits-Oxygenatoren;
-   extrakorporale Kreisläufe (Blutschlauchsysteme);
-   separate Wärmeaustauscher;
-   separate Hilfsgeräte.

Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) (ISO 7199:2009 + Amd 1:2012)

L'ISO 7199:2009 précise les prescriptions relative aux échangeurs gaz/sang extracorporels stériles (oxygénateurs), à usage unique, destinés à oxygéner le sang des patients et à en éliminer le dioxyde de carbone.
L'ISO 7199:2009 s'applique également aux échangeurs thermiques qui font partie intégrante des oxygénateurs extracorporels, et aux seuls accessoires nécessaires à l'utilisation du dispositif.

Vsadki (implantati) za srce in ožilje ter umetni organi - Izmenjevalniki krvnih plinov (ISO 7199:2009 + Amd 1:2012)

Standard EN ISO 7199 + A1 določa zahteve za sterilne zunajtelesne izmenjevalnike krvnih plinov za enkratno uporabo, ki so namenjeni za dovajanje kisika in odvajanje ogljikovega dioksida iz človeške krvi.

General Information

Status
Withdrawn
Public Enquiry End Date
29-Apr-2014
Publication Date
04-Sep-2014
Withdrawal Date
27-Feb-2017
Technical Committee
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
21-Feb-2017
Due Date
16-Mar-2017
Completion Date
28-Feb-2017

RELATIONS

Effective Date
01-Oct-2014

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SLOVENSKI STANDARD
SIST EN ISO 7199:2014
01-oktober-2014
1DGRPHãþD
SIST EN 12022:2000

Vsadki (implantati) za srce in ožilje ter umetni organi - Izmenjevalniki krvnih plinov

(ISO 7199:2009 + Amd 1:2012)

Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO

7199:2009 + Amd 1:2012)

Kardiovaskuläre Implantate und künstliche Organe - Blutgasaustauscher (Oxygenatoren)

(ISO 7199:2009 + Amd 1:2012)

Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels

(oxygénateurs) (ISO 7199:2009 + Amd 1:2012)
Ta slovenski standard je istoveten z: EN ISO 7199:2014
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 7199:2014 en

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------
SIST EN ISO 7199:2014
---------------------- Page: 2 ----------------------
SIST EN ISO 7199:2014
EUROPEAN STANDARD
EN ISO 7199
NORME EUROPÉENNE
EUROPÄISCHE NORM
August 2014
ICS 11.040.40 Supersedes EN 12022:1999
English Version
Cardiovascular implants and artificial organs - Blood-gas
exchangers (oxygenators) (ISO 7199:2009 + Amd 1:2012)

Implants cardiovasculaires et organes artificiels - Kardiovaskuläre Implantate und künstliche Organe -

Échangeurs gaz/sang extracorporels (oxygénateurs) (ISO Blutgasaustauscher (Oxygenatoren) (ISO 7199:2009 + Amd

7199:2009 + Amd 1:2012) 1:2012)
This European Standard was approved by CEN on 17 July 2014.

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

© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 7199:2014 E

worldwide for CEN national Members.
---------------------- Page: 3 ----------------------
SIST EN ISO 7199:2014
EN ISO 7199:2014 (E)
Contents Page

Foreword ..............................................................................................................................................................3

Annex ZA (informative) Relationship between this European Standard and the Essential

Requirements of EU Directive 93/42/EEC on medical devices ......................................................................4

---------------------- Page: 4 ----------------------
SIST EN ISO 7199:2014
EN ISO 7199:2014 (E)
Foreword

The text of ISO 7199:2009 + Amd 1:2012 has been prepared by Technical Committee ISO/TC 150 “Implants

for surgery” of the International Organization for Standardization (ISO) and has been taken over as EN

ISO 7199:2014 by 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 February 2015, and conflicting national standards shall be withdrawn

at the latest by February 2015.

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 12022:1999.

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.

Endorsement notice

The text of ISO 7199:2009 + Amd 1:2012 has been approved by CEN as EN ISO 7199:2014 without any

modification.
---------------------- Page: 5 ----------------------
SIST EN ISO 7199:2014
EN ISO 7199:2014 (E)
Annex ZA
(informative)
Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC on medical devices

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 Essential Requirements of the

New Approach Directive 93/42/EEC on medical devices.

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 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.

Table ZA.1 — Correspondence between this European Standard and Directive 93/42/EEC on

medical devices
Clause(s)/sub-clause(s) Essential Requirements (ERs) of
Qualifying remarks/Notes
of this EN Directive 93/42/EEC
4.1.1; 4.1.2; 5.2; 6.2.1; 6.2.2; 6.3 7.2 Some redundancies, but all
these EN sections address
performance and sterility
issues.
4.3.3; 5.2; 5.4.3 7.3
4.2.1; 4.2.2; 4.2.4 7.5
4.1.1; 6.2.1; 6.2.2; 6.3 8.1
6.2.1; 6.2.2; 6.3 8.3
6.2.1; 6.2.2; 6.3 8.4
4.1.1; 5.2.1; 6.2.1; 6.2.2; 6.2.3 8.5
6.2.1 8.6
6.1; 6.2.1 8.7
4.2.4 9.1
6.1; 6.2; 6.3 13

WARNING — Other requirements and other EU Directives may be applicable to the product(s) falling within

the scope of this standard.
---------------------- Page: 6 ----------------------
SIST EN ISO 7199:2014
INTERNATIONAL ISO
STANDARD 7199
Second edition
2009-04-15
Cardiovascular implants and artificial
organs — Blood-gas exchangers
(oxygenators)
Implants cardiovasculaires et organes artificiels — Échangeurs
gaz/sang extracorporels (oxygénateurs)
Reference number
ISO 7199:2009(E)
ISO 2009
---------------------- Page: 7 ----------------------
SIST EN ISO 7199:2014
ISO 7199:2009(E)
PDF disclaimer

This PDF file may contain embedded typefaces. In accordance with Adobe's licensing policy, this file may be printed or viewed but

shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In

downloading this file, parties accept therein the responsibility of not infringing Adobe's licensing policy. The ISO Central Secretariat

accepts no liability in this area.
Adobe is a trademark of Adobe Systems Incorporated.

Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-creation

parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies. In

the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below.

COPYRIGHT PROTECTED DOCUMENT
© ISO 2009

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 either ISO at the address below or

ISO's member body in the country of the requester.
ISO copyright office
Case postale 56 • CH-1211 Geneva 20
Tel. + 41 22 749 01 11
Fax + 41 22 749 09 47
E-mail copyright@iso.org
Web www.iso.org
Published in Switzerland
ii © ISO 2009 – All rights reserved
---------------------- Page: 8 ----------------------
SIST EN ISO 7199:2014
ISO 7199:2009(E)
Contents Page

Foreword............................................................................................................................................................ iv

Introduction ........................................................................................................................................................ v

1 Scope ..................................................................................................................................................... 1

2 Normative references ........................................................................................................................... 1

3 Terms and definitions........................................................................................................................... 2

4 Requirements ........................................................................................................................................ 3

4.1 Biological characteristics .................................................................................................................... 3

4.2 Physical characteristics....................................................................................................................... 3

4.3 Performance characteristics ............................................................................................................... 3

5 Tests and measurements to determine compliance with this International Standard.................. 4

5.1 General................................................................................................................................................... 4

5.2 Biological characteristics .................................................................................................................... 4

5.3 Physical characteristics....................................................................................................................... 5

5.4 Performance characteristics ............................................................................................................... 5

6 Information supplied by the manufacturer ........................................................................................8

6.1 Information to be given on the oxygenator........................................................................................ 8

6.2 Information to be given on the packaging ......................................................................................... 8

6.3 Information to be given in the accompanying documents............................................................... 9

6.4 Information to be given in the accompanying documents in a prominent form.......................... 10

7 Packaging ............................................................................................................................................ 10

Bibliography ..................................................................................................................................................... 11

© ISO 2009 – All rights reserved iii
---------------------- Page: 9 ----------------------
SIST EN ISO 7199:2014
ISO 7199:2009(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.

ISO 7199 was prepared by Technical Committee ISO/TC 150, Implants for surgery, Subcommittee SC 2,

Cardiovascular implants and extracorporeal systems.

This second edition cancels and replaces the first edition (ISO 7199:1996), which has been technically revised.

iv © ISO 2009 – All rights reserved
---------------------- Page: 10 ----------------------
SIST EN ISO 7199:2014
ISO 7199:2009(E)
Introduction

This International Standard is intended to ensure that devices designed to affect the exchange of gases in

support of, or as a substitution for, the normal respiratory function of the lungs have been adequately tested

for both their safety and function, and that extracorporeal device characteristics are appropriately disclosed

when labeling the device.

This International Standard therefore contains procedures to be used for evaluation of extracorporeal blood-

gas exchangers (oxygenators). Type test procedures for determination of the gas transfer, blood cell damage

and heat exchanger performance are described, although limits for these characteristics are not specified.

Ready identification of the performance characteristics should, however, assist the user in the selection of an

oxygenator that will suit the needs of the patient.

This International Standard also includes minimum reporting requirements, which will allow the user to

compare performance characteristics of oxygenators of different designs in a standard way.

This International Standard makes reference to other International Standards in which methods for

determination of characteristics common to medical devices can be found.

No provisions have been made for quantification of microbubble generation or for non-formed elements of

bovine blood because there currently is no consensus regarding satisfactorily reproducible test methods.

Requirements for animal and clinical studies have not been included in this International Standard. Such

studies may be parts of a manufacturer's quality system.

This International Standard contains only those requirements that are specific to oxygenators. Non-specific

requirements are covered by references to other International Standards listed in the normative references

section. Since non-toxicity is anticipated to be the subject of a future horizontal/level 1 standard, this

International Standard does not cover non-toxicity.
© ISO 2009 – All rights reserved v
---------------------- Page: 11 ----------------------
SIST EN ISO 7199:2014
---------------------- Page: 12 ----------------------
SIST EN ISO 7199:2014
INTERNATIONAL STANDARD ISO 7199:2009(E)
Cardiovascular implants and artificial organs — Blood-gas
exchangers (oxygenators)
1 Scope

This International Standard specifies requirements for sterile, single-use, extracorporeal blood-gas

exchangers (oxygenators) intended for supply of oxygen to, and removal of carbon dioxide from, the blood of

humans.

This International Standard also applies to heat exchangers that are integral parts of oxygenators and to external

equipment unique to the use of the device.
This International Standard does not apply to:
⎯ implanted oxygenators;
⎯ liquid oxygenators;
⎯ extracorporeal circuits (blood tubing);
⎯ separate heat exchangers;
⎯ separate ancillary devices.
2 Normative references

The following referenced documents are indispensable for the application of this document. For dated

references, only the edition cited applies. For undated references, the latest edition of the referenced

document (including any amendments) applies.

ISO 10993-1, Biological evaluation of medical devices — Part 1: Evaluation and testing

ISO 10993-7, Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals

ISO 10993-11, Biological evaluation of medical devices — Part 11: Tests for systemic toxicity

ISO 11135:1994, Medical devices — Validation and routine control of ethylene oxide sterilization

ISO 11137-1, Sterilization of health care products — Radiation — Part 1: Requirements for development,

validation and routine control of a sterilization process for medical devices

ISO 11607-1, Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile

barrier systems and packaging systems

ISO 11607-2, Packaging for terminally sterilized medical devices — Part 2: Validation requirements for

forming, sealing and assembly processes

ISO 17665-1, Sterilization of health care products — Moist heat — Part 1: Requirements for the development,

validation and routine control of a sterilization process for medical devices
© ISO 2009 – All rights reserved 1
---------------------- Page: 13 ----------------------
SIST EN ISO 7199:2014
ISO 7199:2009(E)
3 Terms and definitions
For the purposes of this document, the following terms and definitions apply.
3.1
blood-gas exchanger
oxygenator

extracorporeal device designed to supplement, or be a substitute for, the respiratory function of the lungs

3.2
blood pathway
paths of the oxygenator containing blood during intended clinical use
3.3
gas pathway

parts of the oxygenator containing the ventilation gas during intended clinical use

3.4
heat exchanger

component that is intended to control the temperature of the circulating blood or priming solution

3.5
heat exchanger performance factor

ratio of the difference between the temperature of blood at the outlet of the oxygenator and the temperature of

blood at the inlet of the oxygenator to the difference between the temperature of the water at the inlet of the

heat exchanger and the temperature of blood at the inlet of the oxygenator
3.6
integral part

part that is connected to the oxygenator and cannot normally be separated by the user

3.7
operating variables
settings of controls that affect the function of the device
3.8
platelet reduction

percentage reduction of platelets contained in a circuit incorporating an oxygenator, less the percentage

reduction in an identical control circuit without an oxygenator, as a function of time

3.9
plasma-free haemoglobin level

concentration of plasma-free haemoglobin in a circuit incorporating an oxygenator, less the concentration in

an identical control circuit without an oxygenator, as a function of time
3.10
white blood cell reduction

percentage reduction of white blood cells contained in a circuit incorporating an oxygenator, less the

percentage reduction in an identical control circuit without an oxygenator, as a function of time

3.11
residual blood volume

difference between the priming volume of the unit and the blood volume that can be e

...

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.UD]SRUHGImplants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) - Amendement 1: Éclaircissements pour les méthodologies d'essai, le marquage et le plan d'échantillonnage (ISO 7199:2009 + Amd 1:2012)Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) - Amendment 1: Clarifications for test methodologies, labelling, and sampling schedule (ISO 7199:2009 + Amd 1:2012)11.040.40Implantanti za kirurgijo, protetiko in ortetikoImplants for surgery, prosthetics and orthoticsICS:Ta slovenski standard je istoveten z:FprEN ISO 7199kSIST FprEN ISO 7199:2014en01-april-2014kSIST FprEN ISO 7199:2014SLOVENSKI

STANDARD
kSIST FprEN ISO 7199:2014
EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM
FINAL DRAFT
FprEN ISO 7199
January 2014 ICS 11.040.40 Will supersede EN 12022:1999English Version

Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) - Amendment 1: Clarifications for test methodologies, labelling, and sampling schedule (ISO 7199:2009 + Amd 1:2012)

Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) - Amendement 1: Éclaircissements pour les méthodologies d'essai, le marquage et le plan d'échantillonnage (ISO 7199:2009 + Amd 1:2012)

Kardiovaskuläre Implantate und künstliche Organe - Blutgasaustauscher (Oxygenatoren) - Erläuterungen hinsichtlich Prüfverfahren, Kennzeichnung und Probenahmeplan This draft European Standard is submitted to CEN members for unique acceptance procedure. It has been drawn up by the Technical Committee CEN/TC 205.

If this draft becomes a European Standard, 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.

This draft European Standard was established by CEN 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.

Recipients of this draft are invited to submit, with their comments, notification of any relevant patent rights of which they are aware and to provide supporting documentation.

Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and shall not be referred to as a European Standard.

EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre:
Avenue Marnix 17,

B-1000 Brussels © 2014 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. FprEN ISO 7199:2014 EkSIST FprEN ISO 7199:2014

FprEN ISO 7199:2014 (E) 2 Contents Page Foreword ..............................................................................................................................................................3 Annex ZA (informative)

Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC on medical devices .........................................................4

kSIST FprEN ISO 7199:2014

FprEN ISO 7199:2014 (E) 3 Foreword The text of ISO 7199:2009 + Amd 1:2012 has been prepared by Technical Committee ISO/TC 150 “Implants for surgery” of the International Organization for Standardization (ISO) and has been taken over as FprEN ISO 7199:2014 by Technical Committee CEN/TC 205 “Non-active medical devices” the secretariat of which is held by DIN. This document is currently submitted to the Unique Acceptance Procedure. This document will supersede EN 12022:1999. 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. Endorsement notice The text of ISO 7199:2009 + Amd 1:2012 has been approved by CEN as FprEN ISO 7199:2014 without any modification. kSIST FprEN ISO 7199:2014

FprEN ISO 7199:2014 (E) 4 Annex ZA (informative)

Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC on medical devices 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 Essential Requirements of the New Approach Directive 93/42/EEC on medical devices.

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 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.

Table ZA.1 — Correspondence between this European Standard and Directive 93/42/EEC on medical devices Clause(s)/sub-clause(s) of this EN Essential Requirements (ERs) of Directive 93/42/EEC Qualifying remarks/Notes 4.1.1; 4.1.2; 5.2; 5.3; 6.2.1; 6.2.2; 6.3.1 7.2 Some redundancies, but all these EN sections address performance and sterility issues. 4.1.2; 4.3.3; 5.2; 5.4.3 7.3

4.2.1; 4.2.2; 4.2.4 7.5
4.1.1; 6.2.1; 6.2.2; 6.3.1 8.1
6.2.1; 6.2.2; 6.3.1 8.3
6.2.1; 6.2.2; 6.3.1 8.4
6.2.1; 6.2.2; 6.3.1 8.5 Partly addressed only. 6.2.1 8.6
6.1; 6.2.1 8.7
4.2.4 9.1
4.3 10.1
4.3 10.2 Partly addressed. 6.1; 6.2; 6.3 13

WARNING — Other requirements and other EU Directives may be applicable to the product(s) falling within the scope of this standard. kSIST FprEN ISO 7199:2014

Reference numberISO 7199:2009(E)© ISO 2009

INTERNATIONAL STANDARD ISO7199Second edition2009-04-15Cardiovascular implants and artificial organs — Blood-gas exchangers (oxygenators) Implants cardiovasculaires et organes artificiels — Échangeurs gaz/sang extracorporels (oxygénateurs)

kSIST FprEN ISO 7199:2014

ISO 7199:2009(E) PDF disclaimer This PDF file may contain embedded typefaces. In accordance with Adobe's licensing policy, this file may be printed or viewed but shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In downloading this file, parties accept therein the responsibility of not infringing Adobe's licensing policy. The ISO Central Secretariat accepts no liability in this area. Adobe is a trademark of Adobe Systems Incorporated. Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-creation parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies. In the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below.

COPYRIGHT PROTECTED DOCUMENT

ISO 2009 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 either ISO at the address below or ISO's member body in the country of the requester. ISO copyright office Case postale 56 • CH-1211 Geneva 20 Tel.

+ 41 22 749 01 11 Fax
+ 41 22 749 09 47 E-mail
copyright@iso.org Web
www.iso.org Published in Switzerland
ii © ISO 2009 – All rights reserved
kSIST FprEN ISO 7199:2014

ISO 7199:2009(E) © ISO 2009 – All rights reserved iiiContents Page Foreword............................................................................................................................................................iv Introduction........................................................................................................................................................v 1 Scope.....................................................................................................................................................1 2 Normative references...........................................................................................................................1 3 Terms and definitions...........................................................................................................................2 4 Requirements........................................................................................................................................3 4.1 Biological characteristics....................................................................................................................3 4.2 Physical characteristics.......................................................................................................................3 4.3 Performance characteristics...............................................................................................................3 5 Tests and measurements to determine compliance with this International Standard..................4 5.1 General...................................................................................................................................................4 5.2 Biological characteristics....................................................................................................................4 5.3 Physical characteristics.......................................................................................................................5 5.4 Performance characteristics...............................................................................................................5 6 Information supplied by the manufacturer........................................................................................8 6.1 Information to be given on the oxygenator........................................................................................8 6.2 Information to be given on the packaging.........................................................................................8 6.3 Information to be given in the accompanying documents...............................................................9 6.4 Information to be given in the accompanying documents in a prominent form..........................10 7 Packaging............................................................................................................................................10 Bibliography.....................................................................................................................................................11

kSIST FprEN ISO 7199:2014

ISO 7199:2009(E) iv © ISO 2009 – All rights reserved 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. ISO 7199 was prepared by Technical Committee ISO/TC 150, Implants for surgery, Subcommittee SC 2, Cardiovascular implants and extracorporeal systems. This second edition cancels and replaces the first edition (ISO 7199:1996), which has been technically revised.

kSIST FprEN ISO 7199:2014

ISO 7199:2009(E) © ISO 2009 – All rights reserved vIntroduction This International Standard is intended to ensure that devices designed to affect the exchange of gases in support of, or as a substitution for, the normal respiratory function of the lungs have been adequately tested for both their safety and function, and that extracorporeal device characteristics are appropriately disclosed when labeling the device. This International Standard therefore contains procedures to be used for evaluation of extracorporeal blood-gas exchangers (oxygenators). Type test procedures for determination of the gas transfer, blood cell damage and heat exchanger performance are described, although limits for these characteristics are not specified. Ready identification of the performance characteristics should, however, assist the user in the selection of an oxygenator that will suit the needs of the patient. This International Standard also includes minimum reporting requirements, which will allow the user to compare performance characteristics of oxygenators of different designs in a standard way. This International Standard makes reference to other International Standards in which methods for determination of characteristics common to medical devices can be found. No provisions have been made for quantification of microbubble generation or for non-formed elements of bovine blood because there currently is no consensus regarding satisfactorily reproducible test methods. Requirements for animal and clinical studies have not been included in this International Standard. Such studies may be parts of a manufacturer's quality system. This International Standard contains only those requirements that are specific to oxygenators. Non-specific requirements are covered by references to other International Standards listed in the normative references section. Since non-toxicity is anticipated to be the subject of a future horizontal/level 1 standard, this International Standard does not cover non-toxicity.

kSIST FprEN ISO 7199:2014
kSIST FprEN ISO 7199:2014

INTERNATIONAL STANDARD ISO 7199:2009(E) © ISO 2009 – All rights reserved 1Cardiovascular implants and artificial organs — Blood-gas exchangers (oxygenators) 1 Scope This International Standard specifies requirements for sterile, single-use, extracorporeal blood-gas exchangers (oxygenators) intended for supply of oxygen to, and removal of carbon dioxide from, the blood of humans. This International Standard also applies to heat exchangers that are integral parts of oxygenators and to external equipment unique to the use of the device. This International Standard does not apply to: ⎯ implanted oxygenators; ⎯ liquid oxygenators; ⎯ extracorporeal circuits (blood tubing); ⎯ separate heat exchangers; ⎯ separate ancillary devices. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 10993-1, Biological evaluation of medical devices — Part 1: Evaluation and testing ISO 10993-7, Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals ISO 10993-11, Biological evaluation of medical devices — Part 11: Tests for systemic toxicity ISO 11135:1994, Medical devices — Validation and routine control of ethylene oxide sterilization ISO 11137-1, Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices ISO 11607-1, Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems ISO 11607-2, Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes ISO 17665-1, Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices kSIST FprEN ISO 7199:2014

ISO 7199:2009(E) 2 © ISO 2009 – All rights reserved 3 Terms and definitions For the purposes of this document, the following terms and definitions apply. 3.1 blood-gas exchanger oxygenator extracorporeal device designed to supplement, or be a substitute for, the respiratory function of the lungs 3.2 blood pathway paths of the oxygenator containing blood during intended clinical use 3.3 gas pathway parts of the oxygenator containing the ventilation gas during intended clinical use 3.4 heat exchanger component that is intended to control the temperature of the circulating blood or priming solution 3.5 heat exchanger performance factor R ratio of the difference between the temperature of blood at the outlet of the oxygenator and the temperature of blood at the inlet of the oxygenator to the difference between the temperature of the water at the inlet of the heat exchanger and the temperature of blood at the inlet of the oxygenator 3.6 integral part part that is connected to the oxygenator and cannot normally be separated by the user 3.7 operating variables settings of controls that affect the function of the device 3.8 platelet reduction percentage reduction of platelets contained in a circuit incorporating an oxygenator, less the percentage reduction in an identical control circuit without an oxygenator, as a function of time 3.9 plasma-free haemoglobin level concentration of plasma-free haemoglobin in a circuit incorporating an oxygenator, less the concentration in an identical control circuit without an oxygenator, as a function of time 3.10 white blood cell reduction percentage reduction of white blood cells contained in a circuit incorporating an oxygenator, less the percentage reduction in an identical control circuit without an oxygenator, as a function of time 3.11 residual blood volume difference between the priming volume

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