Response I received from Ti today suggests that the MSP430 could be used so long as "officers of the parties have executed an agreement specifically governing such use". While our product(s) are neither life supporting nor sustaining, but implantable nevertheless, with whom should we interface with to execute such as agreement if still required? It was again suggested I post here for a response, so there you go ... Incidentally, over 80% of implants currently use the MSP430, so unsure if this is a new requirement. Look forward to your urgent response, thank you.