Bio-Rad ZOE™ Fluorescent Cell Imager - Manual (Page 5)

| iii ZOE Fluorescent Cell Imager Instruction Manual | iii
Safety Compliance
This instrument has been tested and found to be in compliance with all applicable requirements of the following safety and
electromagnetic standards:
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EN 61010-1:2010 — Electrical Equipment for Measurement, Control, and Laboratory Use
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UL Std No. 61010-1:2012 — Electrical Equipment for Measurement, Control, and Laboratory Use, Part 1: General Requirements
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CAN/CSA C22.2 No. 61010-1-12 — Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use,
Part 1: General Requirements
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IEC 61010-1:2010 — Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use, Part 1
General Requirements
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IEC62471 Photobiological Safety of Lamps and Lamp Systems
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EN62471 Photobiological Safety of Lamps and Lamp Systems
Electromagnetic Compatibility (EMC)
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F.C.C. Title 47 Part 15B as a Class A digital device
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IEC/EN61326-1 Class A Electrical Equipment for Measurement, Control, and Laboratory Use — General Requirements
FCC Warning and Notes
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Warning: Changes or modifications to this unit not expressly approved by the party responsible for compliance could void the
user’s authority to operate the equipment
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Note: This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to part 15 of
the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when the equipment
is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not
installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation
of this equipment in a residential area is likely to cause harmful interference, in which case the user will be required to correct the
interference at the user’s own expense
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Note regarding FCC compliance: Although this design of instrument has been tested and found to comply with Part 15, Subpart
B, of the FCC Rules for a Class A digital device, please note that this compliance is voluntary, as the instrument qualifies as an
“exempted device” under 47 CFR 15.103(c) in regard to the cited FCC regulations in effect at the time of manufacture
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Note regarding Canadian EMC compliance: Le present appareil numerique n’emet pas de bruits radioelectrique depassant les
limites applicables aux appareils numeriques de classe A prescrites dans le reglement sur le brouillage radioelectrique edicte par le
Ministere des Communications du Canada
Canada Warning and Notes
This ISM device complies with Canadian ICES-001.
Cet appareil ISM est conforme à la norme NMB-001 du Canada.
This Bio-Rad instrument is designed and certified to meet EN61010* and the EMC requirements of EN61326 (for Class A) safety
standards. Certified products are safe to use when operated in accordance with the instruction manual. This instrument should not
be modified or altered in any way. Alteration of this instrument will cause the following results:
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Void the manufacturer’s warranty
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Void the EN61010 safety certification
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Create a potential safety hazard
Bio-Rad Laboratories is not responsible for any injury or damage caused by the use of this instrument for purposes other than those
for which it is intended, or by modifications of the instrument not performed by Bio-Rad Laboratories or an authorized agent. We
strongly recommend that you follow the safety specifications listed in this section and throughout this manual. Use only the supplied
power cord in the instrument, making sure to choose the plug adaptor that corresponds to the electrical outlets in your region.