Notwithstanding the provisions of Article R. 5222-18-4, where the second-hand in vitro diagnostic medical device which is the subject of the transfer has never been put into service, the file consists solely of the following elements:
1° The acceptance report for the in vitro diagnostic medical device by the person responsible for the transfer, except where the transfer takes place before the physical acceptance of the device concerned;
2° A declaration on their honour by the person responsible for the transfer of the second-hand medical device, in which they certify that the device has never been put into service.