96
The SLA system conforms to applicable requirements of 21 CFR Subchapter J at the date of
manufacture. It is designated a Class I Laser Device by the Center for Devices and Radiological
Health (CDRH). In normal operation, the laser beam is completely confined and the viewing
windows in the Process Module block the UV laser radiation. However, if the laser cover, doors, or
windows, are removed for any reason, the unit becomes a dangerous Class IV laser device. Direct
or reflected laser power from a Class IV laser device can cause eye damage. See
more information.
70696 Revision 1C 27-Aug-08