Zeiss INTRABEAM, Instructions For Use Manual

Page: 73 / 82

Version 6.2
G-30-1767-en
Page 73
INTRABEAM Water Phantom System data
Regulatory information
Ambient conditions
Description Labeling
Classification The medical device is classified according to Ap-
pendix IX of the Medical Device Directive 93/42/EEC
as Class I (with measuring functionality).
CE mark The medical device complies with the essential re-
quirements stipulated in Appendix I of the Medical
Device Directive 93/42/EEC.
In line with appendix XII of the Medical Device Di-
rective 93/42/EEC the medical device is labeled
with .
For operation Temperature
Rel. humidity
(without condensation)
Air pressure
+ 15 °C...+ 40 °C
(59 °F...104 °F)
30 %...75 %
700 hPa...1060 hPa
For transportation
and storage Temperature
Rel. humidity
(without condensation)
Air pressure
- 20 °C...+ 70 °C
(- 4 °F ...158 °F)
10 %...75 %
500 hPa...1060 hPa