Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004)

ISO/TR 14969:2004 provides guidance for the application of the requirements for quality management systems contained in ISO 13485. It does not add to, or otherwise change, the requirements of ISO 13485. It does not include requirements to be used as the basis of regulatory inspection or certification assessment activities.
This guidance can be used to better understand the requirements of ISO 13485 and to illustrate some of the variety of methods and approaches available for meeting the requirements of ISO 13485.

Medizinprodukte - Qualitätssicherungssysteme - Anleitungen zur Anwendung von ISO 13485:2003 (ISO/TR 14969:2004)

Dispositifs médicaux - Systèmes de gestion de qualité - Lignes directrices pour l'application de l'ISO 13485:2003 (ISO/TR 14969:2004)

Medicinski pripomočki - Sistemi vodenja kakovosti - Navodila za uporabo ISO 13485:2003 (ISO/TR 14969:2004)

To tehnično poročilo zagotavlja navodila za uporabo zahtev za sisteme vodenja kakovosti, ki jih zajema ISO 13485. Ne dodaja ali kako drugače spreminja zahtev, ki se uporabljajo kot osnova za predpisano pregledovanje in dejavnosti certifikacijskega ocenjevanja. To vodilo se lahko uporablja za boljše razumevanje zahtev ISO 13485 in predstavitev nekaterih metod in pristopov, ki so na voljo za izpolnjevanje zahtev ISO 13485.

General Information

Status
Withdrawn
Publication Date
07-Jun-2005
Withdrawal Date
01-Mar-2016
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
02-Mar-2016
Completion Date
02-Mar-2016

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SLOVENSKI STANDARD
SIST-TP CEN ISO/TR 14969:2010
01-januar-2010
0HGLFLQVNLSULSRPRþNL6LVWHPLYRGHQMDNDNRYRVWL1DYRGLOD]DXSRUDER,62
 ,6275
Medical devices - Quality management systems - Guidance on the application of ISO
13485:2003 (ISO/TR 14969:2004)
Medizinprodukte - Qualitätssicherungssysteme - Anleitungen zur Anwendung von ISO
13485:2003 (ISO/TR 14969:2004)
Dispositifs médicaux - Systèmes de gestion de qualité - Lignes directrices pour
l'application de l'ISO 13485:2003 (ISO/TR 14969:2004)
Ta slovenski standard je istoveten z: CEN ISO/TR 14969:2005
ICS:
03.120.10 Vodenje in zagotavljanje Quality management and
kakovosti quality assurance
11.040.01 Medicinska oprema na Medical equipment in general
splošno
SIST-TP CEN ISO/TR 14969:2010 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST-TP CEN ISO/TR 14969:2010

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SIST-TP CEN ISO/TR 14969:2010



TECHNICAL REPORT
CEN ISO/TR 14969

RAPPORT TECHNIQUE

TECHNISCHER BERICHT
June 2005
ICS 11.040.01; 03.120.10

English version
Medical devices - Quality management systems - Guidance on
the application of ISO 13485:2003
Dispositifs médicaux - Systèmes de gestion de qualité -
Lignes directrices pour l'application de l'ISO 13485:2003


This Technical Report was approved by CEN on 3 March 2005. It has been drawn up by the Technical Committee CEN/CLC/WG QS.

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, 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
© 2005 CEN All rights of exploitation in any form and by any means reserved Ref. No. CEN ISO/TR 14969:2005 E
worldwide for CEN national Members.

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SIST-TP CEN ISO/TR 14969:2010
CEN ISO/TR 14969:2005 (E)
Foreword
The text of ISO/TR 14969:2004 has been prepared by Technical Committee ISO/TC 210 “Quality
management and corresponding general aspects for medical devices”. The transposition into a CEN
ISO/TR 14969 has been managed by the CEN/CENELEC Co-ordinating Working Group on quality
supplements for medical devices (CEN/CLC/CWG QS) the Secretariat of which is held by DIN in
collaboration with the CEN Management Centre (CMC).
With the publication of CEN ISO/TR 14969:2005 the following standards became obsolete and shall
be withdrawn:

* EN 724:1994 .Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and
EN 46002 for non-active medical devices.,

* EN 928:1995 .In vitro diagnostic systems - Guidance on the application of EN 29001 and EN
46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices.

* EN 50103:1995 .Guidance on the application of EN 29001 and EN 46001 and of EN 29002
and EN 46002 for the active (including active implantable) medical device industry."

It should be noted that the above-mentioned European standards which are not replaced by CEN
ISO/TR 14969:2005, were harmonized under the European Medical Devices Directives (90/385/EEE,
93/42/EEC and (98/79/EC). CEN ISO/TR 14969:2005 is not proposed for harmonization and so does
not provide a presumption of conformity with regard to these European Directives.
2

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SIST-TP CEN ISO/TR 14969:2010

TECHNICAL ISO/TR
REPORT 14969
First edition
2004-10-15

Medical devices — Quality management
systems — Guidance on the application
of ISO 13485:2003
Dispositifs médicaux — Systèmes de gestion de qualité — Lignes
directrices pour l'application de l'ISO 13485:2003




Reference number
ISO/TR 14969:2004(E)
©
ISO 2004

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SIST-TP CEN ISO/TR 14969:2010
ISO/TR 14969:2004(E)
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