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mwa
Have anybody an idea about this norm of ISo regarding medical device.
According to the norm .
Should the declaration and guidance according to IEC 60601 , be accompanied by every device to the customer?
Does this norm give any information about this specific question?
According to the norm .
Should the declaration and guidance according to IEC 60601 , be accompanied by every device to the customer?
Does this norm give any information about this specific question?