Healthcare Professionals

INTRODUCING MEDTRONIC’S MOST COMPREHENSIVE 

 

TEMPORARY EXTERNAL PACEMAKER PORTFOLIO

External Pacemakers

Medtronic external pacemakers are intended for use with a cardiac pacing lead system for temporary single or dual chamber pacing in a clinical environment.

The Next Generation Temporary External Pacemakers

  • Easy to configure and operate
  • Reliable and proven design
  • Seven-year service life
  • Constant Current design

Overview Brochure

Model 5392

5392

Dual Chamber Temporary External Pacemaker

The dual chamber model 5392 is the next generation temporary pacemaker with both single and dual chamber pacing capability. It has enhanced user interface with improved visibility and increased responsiveness. It also features an improved low battery indicator.


Model 53401

54301

Single Chamber Temporary External Pacemaker

Model 53401 is a battery powered, external single chamber pacemaker for temporary use. It provides four common pacing modes including on-demand VVI/AAI (synchronous) and VOO/AOO (asynchronous) as well as burst functionality for managing atrial tachyarrhythmias.



Education and Training Resources

Access a wide range of interactive courses, case studies, videos and presentations.

5392 Video Series

5392 You Tube Series

5392 Dual Chamber Temporary External Pacemaker

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54301 Video Series

You Tube Series

54301 Single Chamber Temporary External Pacemaker

Watch Now

Product Ordering List

Order the following components:

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Surgical Cables

Surgical Cables Model Type Channel Length Device Compatible
5487

5487


5487L

Disposable, short
Disposable, long

A or V


A or V

6


12

Both

4301

58325S

Reusable, small clip

A or V

12

Both

5883

5883S

 

 

5883L

Disposable, small clip, short

Disposable, small clip, long

A or V

 

 

A or V

6

 

 

12

Both

Patient Cables

Other

StreamLine Pacing Leads (Heart Wires)


IMPORTANT INFORMATION ON INDICATIONS, SAFETY AND WARNINGS

For listing of Indications, Contraindications, Warnings, Precautions, and Potential Adverse Events, please refer to the Instructions For Use .