So if we consider Class III Battery powered devices, not connected to a charger, with no patient applied parts, visual inspection and output checks should suffice.
But if the complete equipment can be used whilst plugged into a charger, then it gets tested as Class I/II (depending upon what Class the charger appears to be)?
Class III BF/CF? such as in the case of wall mounted external AED Defib such as FR2?
But ... how is the FR2 marked? And/or what Class does the manufacturer's documentation declare it to be?
