Luminex FLEXMAP 3D User Manual - Manual (Page 14)

WARNING: Do not use this device in close proximity to sources of strong
electromagnetic radiation, for example, unshielded intentional
RF sources, as these may interfere with proper operation
WARNING: Always handle the FLEXMAP 3D ® system according to Luminex
instructions to avoid any possible interference from its
electromagnetic fields.
Lasers
The Luminex ® FLEXMAP 3D ® instrument is classified under FDA 21 CFR 1040.10 and
1040.11 as a Class I laser product consisting of two Class IIIb lasers within the instrument.
The optional bar code reader is a Class II stand-alone component. In accordance with IEC
60825-1, the instrument is classified as Class 1, containing two Class 3b lasers. The optional
bar code reader is a Class II stand-alone component. The FLEXMAP 3D
® complies with IEC
60825-1 and 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice
No. 50, dated June 24, 2007.
The following label appears on the back of the FLEXMAP 3D ® instrument.
FIGURE 3. Laser Warning Label
The following label appears above the laser apertures located inside the optics enclosure
inside the FLEXMAP 3D
® instrument.
FIGURE 4. Avoid Exposure Label
All Class 3b laser apertures are located within the FLEXMAP 3D ® instrument and are
contained within a protective housing, accessible only to trained field service technicians.
When performing routine maintenance, turn power to the system off and disconnect the
power cord.
DANGER: Do not, under any circumstances, remove the FLEXMAP 3D ®
instrument cover. Use of controls or adjustments or performance
Luminex ® FLEXMAP 3D ® Hardware User Manual
4
For research use only. Not for use
in diagnostic procedures.