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#Denville diagnostics generator#

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Hartford, Connecticut, United States, 06102īoca Raton, Florida, United States, 33422 Littleton, Colorado, United States, 80120 Santa Barbara, California, United States, 93105 Sansum Clinic - Santa Barbara Medical Foundation San Francisco, California, United States, 94117 Rancho Mirage, California, United States, 92270 North Hollywood, California, United States, 91602 Newport Beach, California, United States, 92660 Jonesboro, Arkansas, United States, 72401īakersfield, California, United States, 93311īurbank, California, United States, 91505Ĭoncord, California, United States, 94520ĭeer Park, California, United States, 94576 Scottsdale, Arizona, United States, 85258 Patient has a lead extender, adaptor, or capped/abandoned lead.Non-removable dental implants may be included.MRI compatible mechanical, prosthetic, and bioprosthetic heart valves may be included as long as the labeling of these devices allow for MRI scans conducted per this protocol.may be included as long as the labeling of these devices allow MRI scans conducted per this protocol MRI compatible knee replacements, hip replacements, stents, etc.Patient has other non-MRI compatible device or material implanted

neurostimulator, infusion pump, etc.) that has MR labeling that will not allow the MRI scans to be completed. Patient has another existing active implanted medical device (e.g.

#Denville diagnostics generator#

Patient has a device generator battery voltage at elective replacement interval (ERI).

High voltage lead impedance (HVLI) is NOT within range (i.e.

Pacing lead impedance is NOT within range (i.e.

Capture threshold is greater than 2.5 volts at 0.5 ms for RA and RV leads.

Patient has an ICD/CRT-D and is pacemaker dependent.

Patient is 18 years or above, or of legal age to give informed consent specific to state and national law.

Patient has the ability to provide informed consent for study participation and be willing and able to comply with the study procedures.

Patient has a pacemaker, ICD, or CRT device implanted pectorally.

Patient is scheduled for a non-thoracic MRI scan up to 1.5T.

Patient has a clinical indication for a non-thoracic MRI scan, where MRI is the imaging modality of choice that will give adequate results to manage the patient.

Patient's device and all leads must be implanted for at least 6 weeks prior to the scheduled date of the MRI.

Jude Medical pacemaker, ICD, or CRT current generation device listed in the study protocol and any market-released pacing or defibrillation lead.

Patient is implanted with a market-released St.

Why Should I Register and Submit Results?.