Hivatkozási szám

MSZ EN ISO 13485:2012

Dokumentumazonosító

654059

Cím

Orvostechnikai eszközök. Minőségirányítási rendszerek. Szabályozási célú követelmények (ISO 13485:2003)

Angol cím

Medical devices. Quality management systems. Requirements for regulatory purposes (ISO 13485:2003)

Alkalmazási terület

1.1 General This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services. The primary objective of this International Standard is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes some particular requirements for medical devices and excludes some of the requirements of ISO 9001 that are not appropriate as regulatory requirements. Because of these exclusions, organizations whose quality management systems conform to this International Standard cannot claim conformity to ISO 9001 unless their quality management systems conform to all the requirements of ISO 9001 (see Annex B). 1.2 Application All requirements of this International Standard are specific to organizations providing medical devices, regardless of the type or size of the organization. If regulatory requirements permit exclusions of design and development controls (see 7.3), this can be used as a justification for their exclusion from the quality management system. These regulations can provide alternative arrangements that are to be addressed in the quality management system. It is the responsibility of the organization to ensure that claims of conformity with this International Standard reflect exclusion of design and development controls [see 4.2.2 a) and 7.3]. If any requirement(s) in Clause 7 of this International Standard is(are) not applicable due to the nature of the medical device(s) for which the quality management system is applied, the organization does not need to include such a requirement(s) in its quality management system [see 4.2.2 a)]. The processes required by this International Standard, which are applicable to the medical device(s), but which are not performed by the organization, are the responsibility of the organization and are accounted for in the organization’s quality management system [see 4.1 a)]. In this International Standard the terms “if appropriate” and “where appropriate” are used several times. When a requirement is qualified by either of these phrases, it is deemed to be “appropriate” unless the organization can document a justification otherwise. A requirement is considered “appropriate” if it is necessary in order for - the product to meet specified requirements, and/or - the organization to carry out corrective action.

ICS

03.100.70 Irányítási rendszerek

11.040.01 Orvostechnikai berendezések általában

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2012-07-01

A visszavonás napja

2019-03-31

Forrás

idt EN ISO 13485:2012; idt EN ISO 13485:2012/AC:2012; idt ISO 13485:2003

Előd

MSZ EN ISO 13485:2010

Utód

MSZ EN ISO 13485:2016

Módosítás

Kiegészítő információk

SZK-közlemények

2012/10: Helyesbítés

Kapcsolódó európai jogszabály

93/42/EGK A TANÁCS 93/42/EGK IRÁNYELVE (1993. június 14.) az orvostechnikai eszközökről (MDV93); 98/79/EK AZ EURÓPAI PARLAMENT ÉS A TANÁCS 98/79/EK IRÁNYELVE (1998. október 27.) az in vitro diagnosztikai orvostechnikai eszközökről (VITD); 90/385/EGK A TANÁCS IRÁNYELVE (1990. június 20.) az aktív beültethető orvostechnikai eszközökre vonatkozó tagállami jogszabályok közelítéséről (90/385/EGK) (IMD90)

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