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An identifier linking a surgically placed medical device to a specific implant classification group, study cohort, or insurance benefit group. Used in clinical registries, research databases, and billing systems to organize device records for population-level analysis and claims adjudication.

A hemoglobin measurement associated with a patient who has received a surgically placed medical device, such as a ventricular assist device or implantable cardiac monitor. Used to track hematologic status relevant to device performance, patient safety, and post-implant clinical outcomes.

The primary unique key assigned to a surgically placed medical device record within a clinical or registry system. Serves as the definitive reference for linking device data across implant tracking, surgical documentation, claims processing, and post-market surveillance records throughout the device lifecycle.

A sequential or positional number assigned to a surgically placed medical device when a patient has multiple implants or when devices are recorded across repeated procedures. Distinguishes individual device records in clinical data systems to ensure accurate tracking and reporting of each implant.

A coded value that denotes a specific clinical condition, status, or classification associated with a surgically placed medical device, such as whether the device is active, removed, or under recall. Used to filter and segment implant records in clinical registries and device surveillance workflows.

Clinical or operational guidance text associated with the care, handling, or monitoring of a surgically placed medical device. May include post-operative care directives, device programming parameters, or patient self-management instructions documented in the implant record for care coordination purposes.

A system-generated or assigned lookup value used as the primary relational reference for a surgically placed medical device record in a clinical data warehouse or registry. Enables efficient joins across implant, patient, procedure, and claims tables to support reporting and data integration workflows.

The language code associated with documentation or labeling for a surgically placed medical device, such as a pacemaker or joint prosthesis. Used to ensure regulatory compliance and accurate clinical communication in device tracking and implant registries.

The manufacturer surname or brand family name component identifying a surgically placed medical device within device registry records. Used to differentiate device product lines and support traceability in surgical implant tracking and post-market surveillance systems.

The full official registered name of a surgically placed medical device as recorded with regulatory authorities such as the FDA. Used in device tracking, UDI compliance, and post-market surveillance to ensure accurate identification of implanted devices across clinical systems.

A hierarchical classification indicating the anatomical placement depth or administrative tier of a surgically placed medical device within a device registry or clinical data structure. Used to organize and categorize implant records for reporting, retrieval, and clinical decision support.

The regulatory or manufacturer license number assigned to a surgically placed medical device, used to verify device authorization and compliance with FDA or international regulatory standards. Supports traceability and recall management in implant registries and clinical data systems.

A legacy or misapplied data field in implant registry schemas that may capture device pairing status, such as whether a device is used independently or in conjunction with a companion device. Requires data governance review to confirm intended clinical or operational usage.

The enterprise-level unique identifier assigned to a surgically placed medical device across all integrated clinical and administrative systems. Used as the primary cross-system reference for device tracking, UDI reconciliation, and implant registry management throughout the patient care continuum.

The upper boundary value for a measurable parameter associated with a surgically placed medical device, such as maximum stimulation output for a neurostimulator or maximum load rating for an orthopedic implant. Used in clinical monitoring and device performance validation workflows.

The medical record number of the patient in whom a surgically placed medical device has been implanted. Links device registry records to the patient health record, enabling traceability for device recalls, follow-up care, and post-market surveillance reporting.

The middle name or secondary name component of a surgically placed medical device designation within a device registry. May reflect a product sub-series or model variant name used by the manufacturer to differentiate device configurations within a product family.

The lower boundary value for a measurable parameter associated with a surgically placed medical device, such as minimum battery life threshold or minimum therapeutic output level. Used in device performance monitoring and clinical alert configuration within implant management systems.

A contact number associated with the clinical team or device manufacturer representative responsible for a surgically placed medical device. Used to facilitate rapid communication for device-related alerts, recalls, or follow-up care coordination within implant management workflows.

The system username or user identifier of the individual who last updated the record for a surgically placed medical device in the implant registry. Supports audit trail requirements, data governance, and accountability tracking for changes to implant documentation.