3D Systems iPro 8000 SLA Center User Manual page 100

S e r v i c e
8000/9000
User's Manual
The SLA Center 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 Laser Safety for
more information.
40-D043 Revision C 5-May-17
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