The SmartRead™ Medical Device Identifier is intended to determine the manufacturer of an unknown cardiac implanted electronic device (CIED) manufactured by Abbott Laboratories, Biotronik, Boston Scientific Corporation, Medtronic, or Microport.
When CIED information is unavailable, incomplete, or unknown, clinicians can be left searching for answers when time matters. Traditional identification methods can add unnecessary steps to the clinical workflow. SmartRead MDI is designed to bring rapid, non-invasive CIED manufacturer identification directly to the point of care.
Answers when every second counts.
When patients arrive without reliable CIED information, SmartRead MDI helps clinicians quickly identify the implanted device manufacturer.
Confidence starts with knowing what's implanted.
SmartRead MDI provides a simple, non-invasive way to identify the CIED manufacturer when patient records or device cards are unavailable.
A smarter approach to CIED identification.
SmartRead MDI helps health systems bring fast, consistent device identification to the teams and settings where patients receive care.
The SmartRead™ Medical Device Identifier is intended to determine the manufacturer of an unknown cardiac implanted electronic device (CIED) manufactured by Abbott Laboratories, Biotronik, Boston Scientific Corporation, Medtronic, or Microport. The SmartRead is authorized as a Class II medical device by the FDA for marketing and sale in the United States. The DeNovo request was granted on 9/29/2026
Practices, Imaging Centers, and Hospital Departments can use SmartRead MDI. It is designed to eliminate mis-matched programmer interrogation and other delays in care.