Physiomed IONOSON-Basic Operating Instructions Manual page 2

Legal Notice
Distribution, reproduction and translation of the software and its documentation (or excerpts thereof) are
prohibited without the prior written consent of PHYSIOMED ELEKTROMEDIZIN AG.
PHYSIOMED ELEKTROMEDIZIN AG reserves the right to change the software and associated data as well
as the documentation without notice. All other rights reserved.
PHYSIOMED ELEKTROMEDIZIN AG
Hutweide 10
D-91220 Schnaittach/Laipersdorf (Germany)
Phone: +49 9126 2587-0
Fax: +49 9126 2587-25
E-Mail: info@physiomed.de
Internet: http://www.physiomed.de
IONOSON-Basic is made in Germany in compliance with the quality requirements of EN ISO
13485:2003+AC:2007, EN ISO 9001:2008 and the applicable safety standards and regulations of the
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices.
The compliance with the regulations mentioned here is indicated by the CE label on the instrument. The
declaration of conformity might be requested from the manufacturer at the address given above.
A conformity check acc. to Annex II, approved by the notified body 1275, was carried out.
Last updated December 10, 2010