EN ISO 10993-4:2002

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)

Migrated from Progress Sheet (TC Comment) (2000-07-10): TC Res. 176/1996: Revision approved (TA/970210) ++ SPP update 1997-09-30. ISO/DIS was not followed by // CEN Enq. To be treated by ++ UAP later. ++ new TC forecast in BP Bli 991025 ++ Contact Mr Vyze ext 850 when processing this project through each stage

Biologische Beurteilung von Medizinprodukten - Teil 4: Auswahl von Prüfungen zur Wechselwirkung mit Blut (ISO 10993-4:2002)

Dieser Teil von ISO 10993 legt allgemeine Anforderungen zur Beurteilung der Wechselwirkungen von Medizinprodukten mit Blut fest.
Dieser Teil enthält:
a)   eine Klassifizierung von für den Kontakt mit Blut vorgesehenen medizinischen und zahnmedizinischen Produkten, die nach der Festlegung in ISO 10993 1 auf der bestimmungsgemäßen Verwendung und Dauer des Kontakts beruht;
b)   die Grundprinzipien, die für die Beurteilung der Wechselwirkungen von Medizinprodukten mit Blut maßgebend sind;
c)   die Begründung für die strukturierte Auswahl von Prüfungen nach bestimmten Kategorien, zusammen mit den Prinzipien und der wissenschaftlichen Grundlage dieser Prüfungen.
Einzelheiten von Prüfanforderungen können wegen des eingeschränkten Wissensstandes und der mangelnden Präzision von Prüfungen auf Wechselwirkungen von Medizinprodukten mit Blut nicht festgelegt werden. Außerdem beschreibt dieser Teil von ISO 10993 die biologische Beurteilung im allgemeinen Sinne und braucht nicht unbedingt eine ausreichende Anleitung für Prüfverfahren für ein bestimmtes Medizinprodukt zu sein.

Evaluation biologique des dispositifs médicaux - Partie 4: Choix des essais concernant les interactions avec le sang (ISO 10993-4:2002)

Biološko ovrednotenje medicinskih pripomočkov - 4. del: Izbira preskusov za ugotavljanje interakcij s krvjo (ISO 10993-4:2002)

General Information

• Status: Withdrawn
• Publication Date: 14-Oct-2002
• Withdrawal Date: 19-May-2009
• ICS: 11.100 - Laboratory medicine
• Technical Committee: CEN/TC 206 - Biocompatibility of medical and dental materials and devices
• Drafting Committee: CEN/TC 206 - Biocompatibility of medical and dental materials and devices
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Start Date: 20-May-2009
• Completion Date: 20-May-2009
• Directive: 90/385/EEC - Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/BC/CEN/89/9 - Joint Standardization request to CEN/CENELEC concerning harmonized standards relating to horizontal aspects in the field of medical devices
• Ref Project: SIST EN ISO 10993-4:2003 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)

Relations

• Replaces: EN 30993-4:1993 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:1992)
• Effective Date: 22-Dec-2008
• Replaced By: EN ISO 10993-4:2009 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)
• Effective Date: 30-May-2009
• Amended By: EN ISO 10993-4:2002/A1:2006 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2002/Amd 1:2006)
• Effective Date: 08-Jun-2022

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 10993-4:2003
01-marec-2003
1DGRPHãþD
SIST EN 30993-4:2000
%LRORãNRRYUHGQRWHQMHPHGLFLQVNLKSULSRPRþNRYGHO,]ELUDSUHVNXVRY]D
XJRWDYOMDQMHLQWHUDNFLMVNUYMR,62
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with
blood (ISO 10993-4:2002)
Biologische Beurteilung von Medizinprodukten - Teil 4: Auswahl von Prüfungen zur
Wechselwirkung mit Blut (ISO 10993-4:2002)
Evaluation biologique des dispositifs médicaux - Partie 4: Choix des essais concernant
les interactions avec le sang (ISO 10993-4:2002)
Ta slovenski standard je istoveten z: EN ISO 10993-4:2002
ICS:
11.100.20 %LRORãNRRYUHGQRWHQMH Biological evaluation of
PHGLFLQVNLKSULSRPRþNRY medical devices
SIST EN ISO 10993-4:2003 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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EUROPEAN STANDARD
EN ISO 10993-4
NORME EUROPÉENNE
EUROPÄISCHE NORM
October 2002
ICS 11.100 Supersedes EN 30993-4:1993
English version
Biological evaluation of medical devices - Part 4: Selection of
tests for interactions with blood (ISO 10993-4:2002)
Evaluation biologique des dispositifs médicaux - Partie 4: Biologische Beurteilung von Medizinprodukten - Teil 4:
Choix des essais concernant les interactions avec le sang Auswahl von Prüfungen zur Wechselwirkung mit Blut (ISO
(ISO 10993-4:2002) 10993-4:2002)
This European Standard was approved by CEN on 19 August 2002.
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 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 Management Centre has the same status as the official
versions.
CEN members are the national standards bodies of Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece,
Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2002 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 10993-4:2002 E
worldwide for CEN national Members.

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EN ISO 10993-4:2002 (E)
CORRECTED  2002-12-11
Foreword
This document (EN ISO 10993-4:2002) has been prepared by Technical Committee ISO/TC 194
"Biological evaluation of medical devices" in collaboration with Technical Committee CEN/TC
206 "Biocompatibility of medical and dental materials and devices", the secretariat of which is
held by NEN.
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 April 2003, and conflicting national
standards shall be withdrawn at the latest by April 2003.
This document supersedes EN 30993-4:1993.
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 ZB, 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, Czech
Republic, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg,
Malta, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and the United Kingdom.
Endorsement notice
The text of ISO 10993-4:2002 has been approved by CEN as EN ISO 10993-4:2002 without any
modifications.
NOTE Normative references to International Standards are listed in Annex ZA (normative).
2

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EN ISO 10993-4:2002 (E)
Annex ZA
(normative)
Normative references to international publications
with their relevant European publications
This European Standard incorporates by dated or undated reference, provisions from other
publications. These normative references are cited at the appropriate places in the text and the
publications are listed hereafter. For dated references, subsequent amendments to or revisions of
any of these publications apply to this European Standard only when incorporated in it by
amendment or revision. For undated references the latest edition of the publication referred to
applies (including amendments).
NOTE Wher
...