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SSH EN ISO 14937:2009

Sterilizimi i produkteve të kujdesit shëndetësor - Kërkesa të përgjithshme për karakterizimin e një agjenti sterilizues dhe zhvillimin, vlerësimin dhe kontrollin e zakonshëm të procesit të sterilizimit për pajisjet mjekësore (ISO 14937:2009)

Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)
23 maj 2011

General information

60.60     23 maj 2011

DPS

DPS/KT 316

European Norm

11.080.01  

anglisht  

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Scope

ISO 14937:2009 specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices.
It applies to sterilization processes in which microorganisms are inactivated by physical and/or chemical means and is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
ISO 14937:2009 specifies the elements of a Quality Management System which are necessary to assure the appropriate characterization of the sterilizing agent, development, validation and routine monitoring and control of a sterilization process.

Related directives

Directives related to this standards.

98/79/EC

Pajisje mjekësore të diagnostikimit "in-vitro"

Të harmonizuara
90/385/EEC

Pajisjet mjekësore aktive transplatuese

Të harmonizuara
93/42/EEC

Pajisje Mjekësore

Të harmonizuara

Life cycle

PREVIOUSLY

WITHDRAWN
SSH EN ISO 14937:2000

NOW

PUBLISHED
SSH EN ISO 14937:2009
60.60 Standard published
23 maj 2011

Related project

Adopted from EN ISO 14937:2009