I believe that you only have to register the class 1 device (non measuring or sterile) with the competent authority where your EU Authorized Representative is located.
One of the important updates of the revised MDD is that:
The manufacturers are permitted only to have 1(one) Authorized Representative for a single product in European Union (EU) “…it is necessary to introduce an obligation for such manufacturers to designate an authorized representative for a device. The designation should be effective at least for all devices of the same model.” (Article 14, section 2)
The manufacturer does not need necessarily to designate the same EC REP for his entire range of medical devices.
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