1.1 Inclusions
1.1.1 This part of ISO 17665 specifies requirements for the development, validation and routine control of a
moist heat sterilization process for medical devices.
NOTE Although the scope of this part of ISO 17665 is limited to medical devices, it specifies requirements and
provides guidance that may be applicable to other health care products.
1.1.2 Moist heat sterilization processes covered by this part of ISO 17665 include but are not limited to:
a) saturated steam venting systems;
b) saturated steam active air removal systems;
c) air steam mixtures;
d) water spray;
e) water immersion.
NOTE See also Annex E.
1.2 Exclusions
1.2.1 This part of ISO 17665 does not specify requirements for development, validation, and routine control
of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine
spongiform encephalopathy and Creutzfeldt-Jakob disease. Specific recommendations have been produced
in particular countries for the processing of materials potentially contaminated with these agents.
NOTE See also ISO 22442-1, ISO 22442-2 and ISO 22442-3.
1.2.2 This part of ISO 17665 does not apply to those sterilization processes that are based on a
combination of moist heat with other biocidal agents (e.g. formaldehyde) as the sterilizing agent.
1.2.3 This part of ISO 17665 does not detail a specified requirement for designating a medical device as
sterile.
NOTE Attention is drawn to national or regional requirements for designating medical devices as sterile. See, for
example, EN 556-1 or ANSI/AAMI ST67.
1.2.4 This part of ISO 17665 does not specify a quality management system for the control of all stages of
production of medical devices.
NOTE It is not a requirement of this part of ISO 17665 to have a complete quality management system during
manufacture, but the elements of a quality management system that are the minimum necessary to control the sterilization
process are normatively referenced at appropriate places in the text (see, in particular, Clause 4). Attention is drawn to the
standards for quality management systems (see ISO 13485) that control all stages of production of medical devices,
including the sterilization process. Regional and national regulations for the provision of medical devices might require
implementation of a complete quality management system and the assessment of that system by a third party.
1.2.5 This part of ISO 17665 does not specify requirements for occupational safety associated with the
design and operation of moist heat sterilization facilities.
NOTE Requirements for operational safety are specified in IEC 61010-2-040. Additionally, safety regulations exist in
some countries.
Diese ÖNORM legt Anforderungen für die Entwicklung, Validierung und Routineüberwachung eines Sterilisationsverfahrens für Medizinprodukte unter Verwendung von feuchter Hitze fest. Zu den durch die Norm erfassten Sterilisationsverfahren mit feuchter Hitze gehören, ohne darauf begrenzt zu sein : Entlüftungssysteme unter Verwendung gesättigten Dampfs; Systeme mit aktiver Luftentfernung unter Verwendung gesättigten Dampfs; Luft-Dampf-Gemische; Wasserberieselung und Eintauchen in Wasser.