This part of IEC 60601 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PERITONEAL DIALYSIS ME EQUIPMENT as defined in 201.3.208, hereafter referred to as PD EQUIPMENT. It applies to PD EQUIPMENT intended for use either by medical staff or under the supervision of medical experts, including PD EQUIPMENT operated by the PATIENT, regardless of whether the PD EQUIPMENT is used in a hospital or domestic environment.

If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This document can also be applied to PD EQUIPMENT used for compensation or alleviation of disease, injury or disability.

These particular requirements do not apply to the DIALYSING SOLUTION, or the DIALYSING SOLUTION CIRCUIT.

Cross References:
IEC 60601-1-2:2014
IEC 60601-1-8:2006
IEC 60601-1-11:2015
IEC 60601-1-6:2010/AMD1:2013
IEC 60601-1-8:2006/AMD1:2012
IEC 60601-1-6:2010
IEC 60601-1-9:2007/AMD1:2013
ISO 80369-1:2010
IEC 60601-1-6:2010/AMD1:2013
IEC 60601-1-6:2010
IEC 60601-1-10:2007
IEC 60601-1-9:2007
IEC 60601-1-10:2007/AMD1:2013


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