EN 45502 vs IEC 60601-1-8

#1
Hello,

I'm working for a company which is developping an active implanted device with an external part which enables the patient to activate and configure the device and to receive information from the implanted part.
The external part shall be compliant with IEC 60601-1-8 whereas the implanted part shall be compliant with EN 45502.
IEC 60601-1-8 requires alarms whereas EN 45502 requires warning.
Can you please explain me the difference between alarms and warning according to those standards?
Shall a warning, which is emitted by the implanted part, be signalled as an alarm on the external part?

Thanks in advance

Best regards

Clément
 
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