Sony UP-27MD Operating Instructions - Page 4

Storage and transport pressure This symbol indicates the acceptable atmospheric pressure range for storage and transport environments. For accessories This symbol indicates the batch code. This symbol indicates "Do not reuse". For customers in the U.S.A. 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. You are cautioned that any changes or modifications not expressly approved in this manual could void your authority to operate this equipment. All interface cables used to connect peripherals must be shielded in order to comply with the limits for a digital device pursuant to Subpart B of part 15 of FCC Rules. If you have any questions about this product, you may call; Sony Customer Information Service Center 1-800222-7669 or http://www.sony.com/ Supplier's Declaration of Conformity Trade Name : SONY Model : UP-27MD Responsible party : Sony Electronics Inc. Address : 16535 Via Esprillo, San Diego, CA 92127 U.S.A. Telephone Number: 858-942-2230 For customers in the U.S.A. Caution Federal law (United States of America) restricts this device to sale by or on the order of a licensed healthcare practitioner. For customers in Canada This unit has been certified according to Standard CAN/CSA-C22.2 No. 60601-1. Important safeguards and notices for use in the medical environments 1. All devices connected to the unit must be certified or compliant according to IEC 60601-1, IEC 60950-1, and IEC 60065 standards and other IEC/ISO standards applicable to the devices. 2. Furthermore, the system as a whole must comply with IEC 60601-1 standards. All peripheral devices connected to the signal input/output sections of the unit constitute the medical-use system, and therefore, the user is responsible for ensuring that the system as a whole complies with IEC 60601-1 standards. If in doubt, consult qualified Sony service personnel. 3. Connecting the unit to other devices may increase the leakage current. 4. For all peripheral devices connected to the unit that operate on commercial power supplies and do not comply with IEC 60601-1 standards, incorporate an isolation transformer that complies with IEC 60601-1 standards and connect to the commercial power supply via the transformer. 5. The unit generates, uses, and may radiate radio frequency energy. If it is not installed and used in accordance with the instruction manual, it may cause interference on other devices. If the unit causes interference (which can be determined by disconnecting the power cord from the unit), try the following. - Relocate the unit with respect to the affected devices. - Connect the unit and the affected devices to different branch circuits. 4