SX1 User Manual
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M-SX1-001-01
1
COMPLIANCE
FDA-CDRH Compliance
Under the US Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH), the
unit complies with the Code of Federal Regulations (CFR), Title 21, Subchapter J, which pertains to laser
safety and labeling. See following link for more information:
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CSA / IEC Compliance
The unit complies with certain standards of the Canadian Standards Association (CSA) and the
International Electrotechnical Commission (IEC).
The unit falls in the Installation Category (Overvoltage Category) II under IEC 664. IEC 664 relates to
impulse voltage levels and insulation coordination. The category is defined as: local level, appliances,
portable equipment, etc., with smaller transient overvoltages than Installation Category (Overvoltage
Category) III.
The unit falls in the Pollution Degree 2 category under IEC 1010-1 and CAN/CSA-C22.2 No. 1010.1. The IEC
standard on Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use
relates to insulation coordination. The CSA standard is on Safety Requirements for Electrical Equipment
for Measurement Control, and Laboratory Use, Part I: General Requirements. The Pollution Degree 2
category is defined as follows: “Normally only non
-conductive pollution occurs. Occasionally, however, a
temporary conductivity caused by conden
sation must be expected.”
CE Compliance
Electronic test equipment is subject to the EMC Directive in the European Union. The EN61326 standard
prescribes both emission and immunity requirements for laboratory, measurement, and control
equipment. This unit has undergone extensive testing according to the European Union Directive and
Standards.
