Contents: External pulse generator
||Dimensions (H x W x T, cm)
||20 x 9.6 x 3.8
||490 (includes battery)
||Standard 9 V, alkaline or lithium
Brief Summary: Prior to using these devices, please review the Instructions for Use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use. Devices depicted may not be available in all countries. Check with your St. Jude Medical representative for product availability in your country.
Indications for Use: The Model 3085 external pulse generator/temporary pacemaker is designed to be used with cardiac stimulation lead systems for temporary atrial, ventricular or A V sequential stimulation. The Model 3085 has applications where such stimulation modes are indicated for therapeutic, rophylactic, or diagnostic purposes. Specific indications include, but are not limited to, the following:
Sick sinus syndrome; Bradycardia with congestive heart failure; Complete heart block; Acute myocardial infarction complicated with heart block; Sinus bradycardia; Cardiac arrest with ventricular systole; Atrial and/or ventricular ectopic arrhythmia; Postoperatively after cardiac surgery; Temporary application during implantation or exchange of a permanent pacemaker. Indication for atrial overdrive stimulation: Supraventricular tachycardia.
Contraindications: There are no contraindications with regards to the use of the Model 3085 for temporary cardiac stimulation for therapy and prevention of arrhythmia. The state of health of the patient, however, can restrict the choice of operational mode and stimulation parameters. For example, a mode of operation with atrial sensing is not suitable or appropriate when atrial fibrillation occurs. This is due to excessive and chaotic frequency of detected fibrillation waves. Overdrive-stimulation therapy must only be used in the atrium. Overdrive-stimulation in the ventricle could cause life threatening ventricular fibrillation
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