Discussion on OBL and OEM test data for submission as per new EUMDR

#1
Hello everyone,

Need clarification on following query,
As our client is under Brand labelling agreement being OBL and device is being manufacture an release by OEM under OBL brand name.

For obtaining CE certificate we understood that will need whole technical documentation as per new EUMDR, but this OEM and OBL have same devices in markets with their own labels and as they are equivalent to each other so is it possible to show all the test data performed on samples of OEM devices as they are equivalent device or we need test reports performed on only OBL device samples for submission to Notified body.

Thanks
 
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