Company Description:
We have produced gamma camera systems since 1983 for the complete nuclear medical market of the nuclear medical diagnostic. We provide for the discriminating and price sensitive market.
All our gamma camera system are remanufactured* according to current medical and technical requirements. The experience and the know-how since more than 35 years form the development of our data and image processing unit Scintron.
This diagnostic prospects are also available for the veterinary market.
Accredited service, constantly care of our hard- and software and time accordant design show our capacities.
Since 1995 MiE America, Inc. has been in business to provide a better service to our america customers. Located is MiE America, Inc. in Elk Grove Village, IL, USA.
Our company is in accordance with EN ISO 9001:2000, EN ISO 13485:2003 + AC: 2007 and Annex II of Directive 93/42/EWG certified. Also, we are registered as Remanufacturer* of medical devices at the FDA. 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.
We have produced gamma camera systems since 1983 for the complete nuclear medical market of the nuclear medical diagnostic. We provide for the discriminating and price sensitive market.
All our gamma camera system are remanufactured* according to current medical and technical requirements. The experience and the know-how since more than 35 years form the development of our data and image processing unit Scintron.
This diagnostic prospects are also available for the veterinary market.
Accredited service, constantly care of our hard- and software and time accordant design show our capacities.
Since 1995 MiE America, Inc. has been in business to provide a better service to our america customers. Located is MiE America, Inc. in Elk Grove Village, IL, USA.
Our company is in accordance with EN ISO 9001:2000, EN ISO 13485:2003 + AC: 2007 and Annex II of Directive 93/42/EWG certified. Also, we are registered as Remanufacturer* of medical devices at the FDA. 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.