Member

Identifies a subordinate or component-level record linked to a parent implant record within a hierarchical data structure. Used to represent accessory devices, sub-components, or related implant items that are tracked individually but associated with a primary implant encounter or order.

Records the municipality where a surgically placed medical device procedure was performed or where the implant supplier is located. Used in device registry reporting, geographic outcomes analysis, and supply chain documentation to identify the location associated with the implant event.

Identifies the FDA regulatory classification tier assigned to a surgically placed medical device, such as Class I, II, or III, based on risk level. Used in compliance tracking, procurement decisions, and clinical documentation to ensure appropriate regulatory handling and patient safety oversight.

A standardized alphanumeric identifier used to classify and uniquely reference a surgically placed medical device within clinical, billing, and supply chain systems. May correspond to UDI, HCPCS, or internal catalog codes used to track procurement, utilization, and reimbursement across encounters.

The portion of a surgically placed medical device cost that a patient is responsible for paying after the insurance deductible is met, calculated as a percentage of the allowed amount. Used in patient billing and benefit coordination to determine member financial liability for implant procedures.

A free-text field used to capture supplemental notes, clinical observations, or operational remarks associated with a surgically placed medical device. Supports documentation of exceptions, special handling instructions, device condition notes, or communication between surgical and administrative staff.

Records the date on which the surgical placement of a medical device was successfully completed. Used in operative documentation, implant registries, and warranty tracking to establish the official implantation date, which anchors follow-up schedules, device lifespan calculations, and post-surgical care timelines.

A privacy protection flag indicating whether a surgically placed device record requires restricted access. When set, limits visibility of implant details such as device type and placement site to authorized clinical staff only, supporting sensitive condition confidentiality.

The total number of surgically placed devices recorded for a patient or clinical encounter. Used in clinical data systems to track multiple implants such as pacemakers, stents, or joint replacements, supporting device inventory, surgical history reporting, and post-implant monitoring.

The country where the surgically placed device was manufactured, approved, or implanted. Used in clinical tracking systems to support regulatory compliance, international device recalls, FDA reporting, and cross-border patient care coordination involving implanted medical devices.

The unique identifier of the user or system that originally created the implant record in the clinical data system. Used in audit trails to establish accountability, track data entry source, and support compliance reviews for surgically placed device documentation.

The calendar date on which the implant record was initially entered into the clinical data system. Used in audit logging and data governance to establish when a surgically placed device was first documented, supporting traceability and regulatory compliance reporting.

The timestamp indicating the exact time an implant record was first entered into the clinical data system. Combined with the created date, supports precise audit trail reconstruction for surgically placed device documentation and clinical data integrity reviews.

The serum creatinine lab value recorded in association with a surgically placed device, used to assess kidney function prior to or following implant procedures. Elevated creatinine may influence device selection, contrast agent use, or post-implant medication management.

The calendar date on which a medical device was surgically placed into a patient. Used in clinical records to establish the start of device active use, support warranty tracking, schedule follow-up monitoring, and calculate device longevity for replacements or recalls.

The combined date and time at which a medical device was surgically placed into a patient. Used in clinical data systems to precisely timestamp implant procedures, supporting operative documentation, device registry submissions, and adverse event timeline analysis.

The Drug Enforcement Administration registration number associated with the prescribing or implanting clinician when controlled substances are used during an implant procedure. Used for regulatory compliance, controlled substance reconciliation, and surgical case documentation in clinical records.

The date of patient death recorded in association with an implanted medical device. Used in clinical registries and device surveillance systems to calculate device longevity, support post-market safety reporting, and fulfill manufacturer or regulatory mortality tracking requirements.

The calendar date on which an implant record was logically removed from the active clinical data system. Used in data governance and audit processes to track record lifecycle, support data retention compliance, and maintain historical accuracy of surgically placed device documentation.

A flag indicating whether an implant record has been logically removed from active clinical data without physical deletion. Used in data management systems to preserve historical device records while excluding them from current reporting, supporting audit trails and data integrity for surgically placed devices.