Mi E America
Medical Devices, 420 Bennett Rd, Elk Grove Village, Illinois, 60007, United States, 51-200 Employees
Phone Number: +18*********
Who is MIE AMERICA
We have been producing gamma cameras and PET systems since 1981 for the complete nuclear imaging medical market of the nuclear medical diagnostic. We provide for the discriminating and pr...
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Headquarters: 420 Bennett Rd, Elk Grove Village, Illinois, 60007, United States
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Date Founded: 1995
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Employees: 51-200
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Revenue: $5 Million to $10 Million
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Active Tech Stack: See technologies
Industry: Medical Devices
SIC Code: 3829
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NAICS Code: 453998 |
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Frequently Asked Questions Regarding MiE America
Answer: MiE America's headquarters are located at 420 Bennett Rd, Elk Grove Village, Illinois, 60007, United States
Answer: MiE America's phone number is +18*********
Answer: MiE America's official website is https://mieamerica.com
Answer: MiE America's revenue is $5 Million to $10 Million
Answer: MiE America's SIC: 3829
Answer: MiE America's NAICS: 453998
Answer: MiE America has 51-200 employees
Answer: MiE America is in Medical Devices
Answer: MiE America contact info: Phone number: +18********* Website: https://mieamerica.com
Answer: We have been producing gamma cameras and PET systems since 1981 for the complete nuclear imaging medical market of the nuclear medical diagnostic. We provide for the discriminating and price sensitive market. All our systems are manufactured and remanufactured* according to current medical and technical requirements. The experience and the know-how since 1974 formed the development of our data and image processing unit called SCINTRON. These diagnostic prospects are also available for the veterinary market Accredited service, constant care of our hardware and software as well as the time accordant design show our capacities. Since 1995 MiE America, Inc. has been in business to provide better service for our North American customers. MiE America, Inc. is located in Elk Grove Village, IL, USA. The MiE GmbH is in accordance with EN ISO 9001:2008, EN ISO 13485:2012 + AC: 2012 certified and our gamma camera systems are with Annex II of Directive 93/42/EWG approved. All systems are new CE labeled. Also, we are registered as Manufacturer and Remanufacturer* of medical devices at the FDA - our systems are 510(k) approved since 1995. This extensive certification is the basis for the manufacture and distribution of medical products on the world market. *Remanufacturer means any person who processes, conditions, renovates, repackages, restores, or does any other act to a finished device that significantly changes the finished device's performance or safety specifications, or intended use.
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