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System&Procedure pack or accessory

#1
We are a manufacturer of ophthalmic devices with a CE mark. In some cases, we put our devices on top of different tables with a motorized column that allows the operator to adjust the total height. The tables we buy from our supplier and they have its own CE mark as class I medical device.
Currently, we treat the tables as an accessory to our system (is mentioned in the IFU but was not tested with our device during EC type-examination ) but according to MDD article 12 we did a risk assessment and we have a written declaration as required in the article 12 of MDD where we state that we have verified the compatibility.

The question is should we treat this as a procedure packs and we need under MDR register also as System&Procedure pack actor or can we treat the tables as an optional accessory only we have added to our device but we have still done internally risk assessment and prepare a written declaration that accessory table is compatible with our device-so no need for System&Procedure pack registration in this case?
Thank you for your comments.
 
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