Class I marketing regulation and supply chain

#1
My company manufactures class I 510k exempt medical device (registered with the FDA) we have our offices in the AU and UK as well. We ship the manufactured product from the US to UK and AU. The UK and AU offices market the product further in other countries (Asia-pacific and EU region respectively) Do we (the US office) is liable for country specific regulations where the product is being marketed? or can our US and UK office take care of the product registrations?.

If it helps, the product label states the address of all the three countries. US office as "manufactured by" and AU and UK offices as "manufactured for"

Thank you!
 
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