This CRF Module is intended to collect details about how a participant's/ subject's implanted device is modified (e.g., battery replacement, lead revision, etc.) while enrolled in a study. If the entire device is explanted, the Devices Log CRF Module should also be used.
Registration Status:
Qualified
Designations:
Designation:
Device Revision/Replacement Log
Tags:
Designations:
Definition:
This CRF Module is intended to collect details about how a participant's/ subject's implanted device is modified (e.g., battery replacement, lead revision, etc.) while enrolled in a study. If the entire device is explanted, the Devices Log CRF Module should also be used.