We have supplied a device to a customer in the USA. His establishment's bio-med engineering department has tested it (as part of routine tests for any new equipment) according to NFPA 99.
They report that it has "excessive sink current" (all leakage current tests according to 60601-1 are well within limits.)
Is anyone familiar with this standard and the relevant tests?
(My understanding is that NFPA 99 is largely concerned with the building and systems of a hospital but does have a section on medical equipment testing).
TIA
Pads
They report that it has "excessive sink current" (all leakage current tests according to 60601-1 are well within limits.)
Is anyone familiar with this standard and the relevant tests?
(My understanding is that NFPA 99 is largely concerned with the building and systems of a hospital but does have a section on medical equipment testing).
TIA
Pads