Perry Baromedical
Tim Labuhn is an accomplished Electrical Engineer with extensive experience in various engineering disciplines, primarily in the medical, military, and automotive sectors. Since March 2013, Tim has served as an Electrical Engineer and Consultant for Medical Systems at Perry Baromedical, specializing in the design of hyperbaric chamber systems. Additionally, Tim has been a Product Development Engineer at OrthoSensor, Inc. since March 2014 and has operated a design engineering practice since March 2001. Previous roles include a Temporary SQA Engineer at MAKO Surgical Corp., Product Manager at Perry Baromedical, Electrical Design Engineer at Lockheed Martin, and Senior Design Engineer at Anspach Companies. Tim Labuhn holds a Bachelor of Science degree in Electrical Engineering from Michigan Technological University.
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Perry Baromedical
Perry Baromedical is a distinguished and internationally recognized brand name, with a history of more than 50 years of design innovation and quality manufacturing in its field. Perry is the only full line manufacturer of hyperbaric chambers in the industry, with its product line encompassing monoplace and multiplace systems. The Company sells its products to Hospitals (Short Term and Long Term Acute Care, Critical Access and Children’s) as well as free standing wound care clinic programs throughout the world. Perry has excelled in the manufacturing, installation and servicing of hyperbaric oxygen therapy systems. Perry has lead the industry with a reputation for doing business with integrity and providing products with superior quality. (www.perrybaromedical.com) Perry Baromedical is a registered medical device manufacturer. Perry Baromedical is an ISO 13485:2003 certified world leader in the manufacture, installation and service of hyperbaric oxygen therapy systems. Hyperbaric Oxygen Chambers are United States Food and Drug Administration (FDA) Class II devices and are controlled by federal law. All systems are designed, manufactured, tested and installed in accordance with the current regulations of the FDA, The American Society of Mechanical Engineers (ASME/PVHO-2) Codes, and the requirements of the National Fire Protection Agency (NFPA). •First to design patient air flow vents •First to introduce the “white” clinically designed monoplace hyperbaric chamber •First to launch a 40 inch acrylic 3 ATA monoplace chamber, still the largest in the market •First to launch an acrylic 3 ATA chamber for two patients •First to have three distinct classes of monoplace units •First to introduce built in breathing system (BIBS) to support double blind studies