Re: Non EU translation requirements
We have approval for our software medical device in S. Korea and have translated the instructions for use into Korean but not the software interface. Of course, translation of software interface would be preferred by customers there but it is not a big enough market for us to incur the cost of maintaining a translated interface. I'm not sure about Chile, but you could look and see if it is mentioned in this document: http :// www .ita.doc.gov/td/health/Chileregs2005.pdf - OBSOLETE BROKEN 404 LINK(s) UNLINKED - PLEASE HELP - REPORT POSTS WITH BROKEN LINKS