Located in Paris, France.
www.impeto-medical.com
contact
Located in San Diego, CA, USA
www.sudoscan.com
contact
Located in Beijing, China
cn.impeto-medical.com
contact
For the rest of the world, please contact us via the contact form
Impeto Medical complies with State and Federal regulations regarding the manufacture and sale of SUDOSCAN and EZSCAN.
European Medical device directive 93/42 (class IIa) and ISO 13485:2016 delivered by SGS Belgium, notified body 1639.
Updated: december 2021
Country | Products |
---|---|
Europe (CE mark) For : Belgium, Denmark, France, Germany, Italy, Luxembourg, Netherlands, Portugal, Romania, Switzerland, Spain, United Kingdom. | SUDOSCAN EZSCAN |
USA (FDA) | SUDOSCAN |
Australia | EZSCAN |
Chile | EZSCAN |
China | SUDOSCAN EZSCAN |
Egypt | SUDOSCAN EZSCAN |
India | SUDOSCAN EZSCAN |
Irak | EZSCAN |
Israel | SUDOSCAN |
Japan | SUDOSCAN |
Jordan | SUDOSCAN EZSCAN |
Kuwait | SUDOSCAN EZSCAN |
Lebanon | SUDOSCAN EZSCAN |
Mexico | SUDOSCAN |
Morocco | SUDOSCAN EZSCAN |
Peru | SUDOSCAN |
Qatar | SUDOSCAN EZSCAN |
Taiwan | SUDOSCAN EZSCAN |
Saudi Arabia | SUDOSCAN EZSCAN |
Ukraine | SUDOSCAN |
United Arab Emirates | SUDOSCAN EZSCAN |
Promotional Communication. The medical devices SUDOSCAN & EZSCAN are regulated health products under the CE certification, Class IIa, according to the European Medical Device directive – SGS Belgium, notified body 1639. The test allows screening and monitoring of peripheral autonomic neuropathies. It can be performed in diabetic patients or in patients suffering from neurological diseases involving small fibers damage. As with any diagnostic test, its results must be interpreted in a global context including the clinic and other examinations performed. Please read the user manual instructions carefully. Contact our office for more information. Last update: 2021/01/12
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