After an implantation period of approx.64 months, it was reported that the device shows the eos status.The icd was explanted.Please note this icd is affected by a field safety corrective action, bio-lqc, initiated in march 2021.
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Prior to the analysis of the device, the quality documents accompanying the manufacturing process for this icd were re-investigated.All production steps were performed accordingly, and in particular the final acceptance test proved the device functions to be as specified.There was no indication of a material or manufacturing problem.Subsequently the device was interrogated.The interrogation could be properly performed and revealed the mos2 battery status.All electrical parameters were verified and showed a normal device behavior.Especially, the current consumption and the battery state of discharge were found normal and as expected.There was no indication of a device malfunction.
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