OK...........So the elephant is leaving the room. So let's continue the discussion as it stands today (6/29/16).
Our NB and EU rep are both located in the UK. As of today I have not heard a thing from either one of them. If we were in noncompliance I'm certain we would have heard from them

. Not to say they are non-compliant but: what are we supposed to do now

How can a UK Notified Body still be entitled to conduct a conformity assessment on the basis of the European Medical Device Directive when they are no longer a member state.

Can they just open up an office in another EU country and it continues "business as usual"? We are under a service/representation contract; does this decision affect (nullify) that agreement

? Does anybody have a clue how this is going to be
handled?
I hope we can shed light on this.
Luis