What is the right procedure for asking to TI an agreement specifically governing such use?
This thread has been locked.
If you have a related question, please click the "Ask a related question" button in the top right corner. The newly created question will be automatically linked to this question.
What is the right procedure for asking to TI an agreement specifically governing such use?
You are asking about this clause from the datasheet?
"No TI components are authorized for use in FDA Class III (or similar life-critical medical equipment) unless authorized officers of the parties
have executed a special agreement specifically governing such use."
Don't know the answer off the top of my head.
I'll research and get back to you.
Thanks,
Dave