SIST EN ISO 10993-10:2003/A1:2006

Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006)

40.20 different than ISO, de-synchronization due to misleading notification from ISO/CS.

Biologische Beurteilung von Medizinprodukten - Teil 10: Prüfungen auf Irritation und Allergien vom verzögerten Typ (ISO 10993-10:2002/A1:2006)

Évaluation biologique des dispositifs médicaux - Partie 10: Essais d'irritation et d'hypersensibilité retardée - Amendement 1 (ISO 10993-10:2002/Amd 1:2006)

Biološko ovrednotenje medicinskih pripomočkov – 10. del: Preskusi draženja in zakasnjene preobčutljivosti – Dopolnilo 1 (ISO 10993-10:2002/Amd 1:2006)

General Information

• Status: Withdrawn
• Publication Date: 30-Sep-2006
• Withdrawal Date: 17-May-2009
• ICS: 11.100.20 - Biological evaluation of medical devices
• Technical Committee: VAZ - Healthcare
• Current Stage: 9900 - Withdrawal (Adopted Project)
• Start Date: 18-May-2009
• Due Date: 10-Jun-2009
• Completion Date: 18-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: EN ISO 10993-10:2002/A1:2006 - Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006)

Relations

• Replaced By: SIST EN ISO 10993-10:2009 - Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006)
• Effective Date: 01-Jul-2009
• Amends: SIST EN ISO 10993-10:2003 - Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002)
• Effective Date: 22-Dec-2008
• Amends: SIST EN ISO 10993-10:2003 - Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002)
• Effective Date: 08-Jun-2022

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 10993-10:2003/A1:2006
01-oktober-2006
%LRORãNRRYUHGQRWHQMHPHGLFLQVNLKSULSRPRþNRY±GHO3UHVNXVLGUDåHQMDLQ
]DNDVQMHQHSUHREþXWOMLYRVWL±'RSROQLOR,62$PG
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type
hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006)
Biologische Beurteilung von Medizinprodukten - Teil 10: Prüfungen auf Irritation und
Allergien vom verzögerten Typ (ISO 10993-10:2002/A1:2006)
Évaluation biologique des dispositifs médicaux - Partie 10: Essais d'irritation et
d'hypersensibilité retardée - Amendement 1 (ISO 10993-10:2002/Amd 1:2006)
Ta slovenski standard je istoveten z: EN ISO 10993-10:2002/A1:2006
ICS:
11.100.20 %LRORãNRRYUHGQRWHQMH Biological evaluation of
PHGLFLQVNLKSULSRPRþNRY medical devices
SIST EN ISO 10993-10:2003/A1:2006 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

EUROPEAN STANDARD
EN ISO 10993-10:2002/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM
July 2006
ICS 11.100

English Version
Biological evaluation of medical devices - Part 10: Tests for
irritation and delayed-type hypersensitivity - Amendment 1 (ISO
10993-10:2002/Amd 1:2006)
Évaluation biologique des dispositifs médicaux - Partie 10: Biologische Beurteilung von Medizinprodukten - Teil 10:
Essais d'irritation et d'hypersensibilité retardée - Prüfungen auf Irritation und Allergien vom verzögerten Typ
Amendement 1 (ISO 10993-10:2002/Amd 1:2006) (ISO 10993-10:2002/A1:2006)
This amendment A1 modifies the European Standard EN ISO 10993-10:2002; it was approved by CEN on 7 July 2006.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this
amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references concerning such
national standards may be obtained on application to the Central Secretariat or to any CEN member.
This amendment 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 Central Secretariat has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania,
Slovakia, Slovenia, 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
© 2006 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 10993-10:2002/A1:2006: E
worldwide for CEN national Members.

---------------------- Page: 2 ----------------------

EN ISO 10993-10:2002/A1:2006 (E)





Foreword


This document (EN ISO 10993-10:2002/A1:2006) 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 January 2007, and conflicting national standards
shall be withdrawn at the latest by January 2007.

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, Cyprus,
Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland,
Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania,
Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.


Endorsement notice

The text of ISO 10993-10:2002/Amd 1:2006 has been approved by CEN as EN ISO 10993-
10:2002/A1:2006 without any modifications.

2

---------------------- Page: 3 ----------------------

EN ISO 10993-10:2002/A1:2006 (E)



ANNEX ZA
(informative)

Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC and 90/385/EEC



This European Standard has been prepared under a mandate given to CEN to provide one means
of conforming to Essential Requirements of the New Approach Directives 93/42/EEC Medical
devices: General and 90/385/EEC Medical devices: Active implantable.

Once this standard is cited in the Official Journal of the European Communities under that Directive
and has been implemented as a national standard in at least one Member State, compliance with
the normative clauses of this International Standard confers, within the limits of the scope of this
International Standard, a presumption of conformity with the relevant Essential Requirements of
those Directives and associated EFTA regulations.

WARNING: Other requirements and other EU Directives may be applicable to the products falling
within the scope of this standard.

3

---------------------- Page: 4 ----------------------

INTERNATIONAL ISO
STANDARD 10993-10
Second edition
2002-09-01
AMENDMENT 1
2006-07-15


Biological evaluation of medical
devices —
Part 10:
Tests for irritation and delayed-type
hypersensitivity
AMENDMENT 1
Évaluation biologique des dispositifs médicaux —
Partie 10: Essais d'irritation et d'hypersensibilité retardée
AMENDEMENT 1




Reference number
ISO 10993-10:2002/Amd.1:2006(E)
©
ISO 2006

-----
...