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The CE-marking indicates that the product has been subject to an
assessment of his conformity with the MDD and that the medical
device fulfills the requirements of the Medical Device Directive
(93/42/EEC).
Please check our website www.pendiq.com or www.diamesco.com
for an updated issue of this manual since issued in March 2017.
Technical changes reserved.
DIQ-IFU-02 (Rev.0 2017.03.30)
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