eego amplifier EE-21x EE-22x User Manual
Rev. 5, DRN-PDO-1664 2 of 26 2016-07-11
MANUFACTURER
eemagine Medical Imaging Solutions GmbH
Gubener Str. 47
D-10243 Berlin, Germany
Phone: +49 (0)30 2904 8404
E-Mail: support@eemagine.com
IMPORTANT NOTICES
Following the European Medical Device Directive 93/42/EEC Annex IX, eego amplifier is a CE class IIa
medical device.
This User Manual only covers the EE-21x and EE-22x variants of the eego amplifier. Refer to
dedicated User Manual for other variants.
For US customers only:
Rx only
Caution: Federal Law (USA) restricts this device to sale by or on the order of a physician.
DISCLAIMER
We have attempted to write this document as accurately as possible. However, mistakes are bound
to occur, and we reserve the right to make changes to the products, which may render parts of this
document invalid.
No part of this document may be copied or reproduced without the explicit permission of the
authors.
To Next Page
Loading...
