OxyFlo Pro User Manual
Revision 1.1 | May 2015
6
equipment in a residential area is likely to cause interference, in which case
the user will be required to correct the interference at his/her own expense.
1.4
EMC Compliance – EC Declaration of Conformity
This equipment meets the intent of Directive 2004/108/EC for
Electromagnetic Compatibility.
Compliance was demonstrated to the following specifications as listed in the
Official Journal of the European Communities.
EN 61326-1:2006
EN 61326-2-1:2006
1.5
Laser Safety
WARNING
Use of controls or adjustments or performance of procedures
other than those specified herein may result in hazardous
radiation exposure.
WARNING
Never apply an OxyFlo Pro probe directly to the eye. The
laser exposure may cause permanent damage to the retina.
OxyFlo Pro is classified as a Class 1 Laser Product in accordance with the
European Standard EN 60825-1:1994 and 21 CFR 1040.10 and 1040.11.
In accordance with the standard, the back panel of the monitor carries the
declaration:
Class 1 Laser Product
OxyFlo Pro incorporates semiconductor laser diode devices operating in
continuous mode and emitting invisible laser radiation at a nominal
operating wavelength of 830nm. The maximum output power at the probe
tip is less than 0.5mW. Laser light emitted from the optical fibre is highly
divergent.
Although the characteristics of the laser radiation place the OxyFlo device
within the Class 1 classification, users should avoid directing the laser
radiation onto the eye.
Applying the probe to any tissue other than the eye is harmless, even over
prolonged time periods.
1.6
OxyFlo Pro Symbols
SN
Serial number
REF
Catalogue number
(product code)