EU MDR - Labilities when a device is discontinued from the Market

#1
When a device is discontinued from the Market, but still few units are in circulation. What are the liabilities that imply to the manufacturer? How to maintain compliance? Will MDR Transition still imply?
 
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#2
Are they being used beyond 'end of life'? (If you have set one and informed users!)
MDR will apply to new devices placed on the market.
 
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