JDS Uniphase RX3 Series, User Manual

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Safety Features and Compliance
The RX3 Series Multichannel Backreflection Meter complies to CE requirements plus UL3101-1
and CAN/CSA-C22.2 No.1010.1 with respect to laser sources. It is classified per Table 2 as a
Class 1 instrument. The following safety features are incorporated into the design of the unit
There is an LED on the front panel indicating when the laser/LED source is on.
Laser Safety Labeling
The RX3 Series Backreflection Meter is classified per Table 2. As required by the FDA standard
21CFR1040.10, an identification label (Figure 1) is placed on the top of the unit showing name
of manufacturer, address, and month and year of manufacture.
Figure 1: Identification Label
A note, as shown in Figure 2, indicating compliance to FDA requirements is silk-screened on
the rear panel of the instrument.
“THIS DEVICE COMPLIES WITH 21CFR1040.10 EXCEPT DEVIATIONS PER LASER NOTICE
N0. 50, JULY 2001”
Figure 2: FDA Compliance Text
A triangular laser safety label, as shown in Figure 3, is located adjacent to output connectors on
the front panel.
Figure 3: Laser Safety Label
A warning label is located on the front of the instrument, as shown in Figure 4, indicating the
IEC Class of laser and applicable standard:
Figure 4: Laser Warning Label
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