C
cjr978
I was hoping that someone on the forum may be able to help. Our German subsiduary wishes to start distributing product in Belgium. All our of products a CE marked Class I and IIa surgical instrumnets and Class IIb surgical implants.
My understanding is that Belgium do not have any special registration requirements in addition to the usual CE marking activity. However the German team seem to believe there are registration requirements with associated costs and a 6 month time delay.
I am assuming they may well be confusing registration for sellling purposes with a requirement to get hospitals and/or insurance companies to actually agree to use our devices - but cant find anything useful on the internet to help.
Can anyone help clarify the situation for me.
Many thanks
Chris
My understanding is that Belgium do not have any special registration requirements in addition to the usual CE marking activity. However the German team seem to believe there are registration requirements with associated costs and a 6 month time delay.
I am assuming they may well be confusing registration for sellling purposes with a requirement to get hospitals and/or insurance companies to actually agree to use our devices - but cant find anything useful on the internet to help.
Can anyone help clarify the situation for me.
Many thanks
Chris