BS EN 60601-2-23:2015 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT as defined in 201.3.63 and hereinafter referred to as ME EQUIPMENT, whether this ME EQUIPMENT is stand alone or part of a system.

This standard applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth.

This standard does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa).

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 standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.


Cross References:
IEC 60601-1-2:2007
EN 60601-1-2:2007
EN 60601-1-2:2007+corrigendum Mar.:2010
IEC 60601-1-8:2006
EN 60601-1-8:2007
EN 60601-1-8:2007+corrigendum Mar.:2010
IEC 60601-2-49:2011
EN 60601-2-49:2015


Replaces BS EN 60601-2-23:2000 which remains current

All current amendments available at time of purchase are included with the purchase of this document.