What is the record retention period for Medical Devices as per Korean Medical Device Act (MDA)

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One of our Medical devices reached the End of Life and the last batch expired and was removed from our Quality Manual however I am waiting for confirmation from the team were their products still out in the field.

Can anyone please help me confirm the requirement/if there are that these device's records should’ve retained even if there are products still out in the field? and what is the duration of record retention and how long the records need to be retained as per the Korean Medical Device Act (MDA).
 
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