Document #OPM/1300, Revision B
CONFIDENTIAL
© 2013 Copyright VTS Medical Systems, LLC
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Notice for Users
FCC Statement
WARNING – FCC Regulations state that any unauthorized changes or modifications to this equipment
not expressly approved by the manufacturer could void the user’s authority to operate this equipment.
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
his own expense.
For part numbers RLM26HD3C and RLM26HD3MC use only the included power supply, model
WSX624M, manufactured by Jerome Industries, to insure compliance with FCC regulations.
Declaration of Conformity
RLM26HD3C, RLM26HD3CNPWR, RLM26HD3MC, RLM26HD3MCNPWR:
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) this device may not cause harmful interference, and (2) this device must accept any interference
received, including interference that may cause undesired operation.
This device has been evaluated to the UL 60601-1 standard:
Equipment evaluated to this standard is not suitable for use in the presence of a flammable anesthetic
mixture with air or with oxygen or nitrous oxide (unless additional tests have been passed). Therefore
this device is not suitable for use in the presence of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide.
Function, Intended Application and Mode of Operation:
HD3 monitors are intended to be used in the displaying and viewing of video and graphics for review and
analysis by trained medical practitioners. The mode of operation for this device is continuous operation.
These devices are classified as Class 1 Equipment:
RLM26HD3C, RLM26HD3CNPWR, RLM26HD3MC, RLM26HD3MCNPWR
Accessory Equipment:
Accessory equipment connected to the analog and digital interfaces must be certified to the respective
IEC standards (i.e. IEC 950 for data processing equipment and IEC 60601-1 for medical equipment).
Furthermore all configurations shall comply with the system standard IEC 60601-1-1. Any equipment
connected to the signal input part or signal output part configures a medical system. Therefore this
equipment, and new configuration, must comply with the requirements of the system standard IEC
60601-1-1.
For a complete list of current certifications, please refer to the Specifications page of this manual.
Part #:
Serial #:
IMPORTANT:
To aid in reporting in the case of loss or theft, or for
service maintenance purposes, please record the
monitor’s part number and serial number in the
space provided. The numbers are located on the
back of the monitor.
