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OBL under the MDR. Which are the obligations of the OEM?

#1
Cheers to all.

I have one questions related to OBL/OEM obligations. I searched on google but I didn't find the answer to what I'm looking for, maybe someone can help me.
So my company (manufacturer/distributor of medical devices) is thinking on starting a business model as an OBL.
From what I understand, under the MDD both the OEM and the OBL needed to have a conformity assessment for obtaining the CE mark.
But now under the MDR, the responsibility for each particular device relies only on the OBL. The OBL is the one who needs to go through a conformity assessment by a NB.
So my question is: does the OEM still needs to have a CE mark for each particular device? What are its obligations? Do they need to have an ISO 13485 QMS implemented?
Or the responsibility for the MD now relies only on the OBL?

Any help would be much appreciated. Thank you.
 
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