Agree with Brian in his YAID [Yet Another It Depends]
But if you are in the real scope of IEC 60601 series standards that also means
you will have a regulatory submission to the likes of FDA, Health Canada, EU
Notified Bodies, etc. There is a lot more overhead for these regulatory
submissions
YAID [Yet Another It Depends].
Instant gratification can be had by looking at the respective TRFs for these
standards. This is a big question that is too scope-dependent. Probably more
apt to compare 62368 with 60601. And have yet to observe a 'practical' test
process at any third-party test la
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