Device with different options for a sub-component - CE marking implications

#1
I have a Class IIa device made of several subassemblies, where all sub-assemblies are delivered to the hopspital and assembled on-site.

One of the sub-assemblies must be chosen from different size options specific to the beds used in the hospital, therefore the part number for the sub-assembly model sold to the hospital is listed on the invoice. That subassembly is essential for the functioning of the device.

My question is: do I need to CE mark the sub-assembly in question individually or is the CE mark present on the overall device sufficient?

Thank you for your help!
 
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#3
Could the customer order the specific sub assemblies seperately? Or is it always a modular kit that is ordered and shipped together? Can they be ordered as a spare part?
The sub assembly is always shipped and installed as part of the device, it is an integral part of it.
It could be ordered as a spare part too but by the manufacturer who would replace it themselves.
 
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