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LFZR88
Hi All
I'm aware this is an old thread, but I wondered if anyone could help me with a question I have for Brazil. We currently have a Class IIb Medical device product registered in Brazil, but are about to extend the range and therefore would like to add this to the existing registration, can anyone help me with requirements and a timeline for this?
Many thanks
I'm aware this is an old thread, but I wondered if anyone could help me with a question I have for Brazil. We currently have a Class IIb Medical device product registered in Brazil, but are about to extend the range and therefore would like to add this to the existing registration, can anyone help me with requirements and a timeline for this?
Many thanks