COVID-19 Update: Astrodyne TDI Provides Life-Sustaining Medical Power Supplies in Times of Crisis

Hackettstown, NJ - As the Coronavirus (COVID-19) continues to spread across the globe, Astrodyne TDI recognizes the urgency behind increased demand for lifesaving medical devices.  Astrodyne TDI’s engineering expertise in developing state of the art medical grade power supplies can be found in ventilators, LVAD’s and other circulatory devices, surgical suites and oxygen concentrators.

Pulmonary management devices are critical for patients with severe COVID-19, to assist or replace breathing function. Astrodyne TDI has unique expertise in the development and manufacture of power supplies used in critical FDA certified devices and their demanding medical environment.

In addition to supporting the increased demand and mitigating key shortages, Astrodyne TDI remains open through this crisis and can provide technical support and sampling within 48 hours of request.   Astrodyne TDI specializes in BF and CF rated power supplies along with certifications in IEC60601-1, required to ensure patient protection. We will be holding a webinar on our current and next generation embedded and external medical power supplies in the near future to aid Medical Industry Engineers in their design activities during this critical time. 

“The outbreak of the novel Coronavirus and associated severe acute respiratory syndrome is changing the way we are working and living day to day.  This is clearly an unprecedented and dynamic situation.  ATDI has taken multiple precautions to protect our employees and continue the production of our life-saving medical products along with our other supported markets,” said Chris Viola CEO Astrodyne TDI.




Astrodyne TDI designs and manufactures Power Supplies and EMI Filters for a variety of markets, including Aerospace, Industrial, Medical, Military, and Semiconductor Manufacturing. To meet the demands of such a wide range of Power Supply and EMI Filter applications, we have extremely flexible manufacturing capabilities combined with a Quality Management system audited for FDA Class III Medical Device support and ISO13485.


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