EN 46003:1999

Quality systems - Medical devices - Particular requirements for the application of EN ISO 9003

General information

99.60 Withdrawal effective   Jun 27, 2007

CEN/CENELEC

CEN/CLC/WG QS CEN/CENELEC Coordinating working group on quality supplements

European Norm

03.120.10   Quality management and quality assurance | 11.040.01   Medical equipment in general

Scope

This European Standard specifies, in conjunction with EN ISO 9003 : 1994, the quality system requirements for the final inspection and test of medical devices excluding in vitro diagnostic medical devices and active implantable medical devices, and is applicable when a medical device supplier's quality system is assessed in accordance with regulatory requirements. NOTE: For sterile medical devices the relevant particular clauses inEN 46002 : 1996 apply as this standard alone is not sufficient for manufacturers of sterile medical devices seeking to comply with regulatory requirements. As part of an assessment by a third party for the purpose of regulatory requirements, the supplier may be required to provide access to confidential data in order to demonstrate compliance with this standard. The supplier may be required to exhibit these data but is not obliged to provide copies for retention.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Harmonized/Supporting

Life cycle

NOW

WITHDRAWN
EN 46003:1999
99.60 Withdrawal effective
Jun 27, 2007

REVISED BY

WITHDRAWN
EN ISO 13485:2003