REGULATORY APPROVALS
FEDERAL COMMUNICATIONS COMMISSION
RADIO FREQUENCY INTERFERENCE STATEMENT
This equipment has been tested and found to comply with the limits for a Class B 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 residential installation.This equipment generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio
communications. However, there is no guarantee that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct the interference by one or more of the following
measures:
Reorient or relocate the receiving antenna
Increase the separation between the equipment and receiver
Connect the equipment into an outlet on a circuit different from that to which the receiver
is connected
Consult the dealer or an experienced radio/TV technician for help
Warning
To assure continued FCC compliance, the user must use only shielded interfacing cables when connecting to
computer or peripheral. Also, any unauthorized changes or modifications to this equipment would void the user’s
authority to operate.
INDUSTRY CANADA COMPLIANCE STATEMENT
This Class B digital apparatus meets all requirements of the Canadian Interface-causing Equipment Regulations. Cet
Appareil numerique de la classe B respecte toutes les exiginces du Reglement sur le material broilleur du Canada.
CE COMPLIANCE FOR EMISSIONS AND IMMUNITY
This device has been tested to comply with the following European standards for emissions and immunity for ITE and
medical equipment: En 55022, En 55024, EN 61000-3-2/3, and EN 60601-1-2.
MEDICAL PRODUCT SAFETY
CONFORMS TO UL STD 60601-1; CERTIFIED TO CSA STD C22.2 NO. 601.1
4007055
The ETL Recognized Component mark on the product label indicates compliance with UL 60601-1 and CSA Std
C22.2 No. 601.1 standards for medical use. These products must be used with a UL listed computer to comply with
UL safety standards.
The label will also indicate IPX1 per UL and CE standards for “drip-proof” water resistance.
Custom, non-programmable waterproof (IPX8) models are also available by special order. This product should not be
used in the presence of a flammable atmosphere such as an anesthetic mixture with air, oxygen, or nitrous oxide.
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