Owner’s Record

The model and serial numbers are located at the rear. Record these numbers in the space provided below. Refer to these numbers whenever you call upon your Sony dealer regarding this product.

Model No. ____________________

Serial No. ____________________

WARNING

To reduce the risk of fire or electric shock, do not expose this apparatus to rain or moisture.

To avoid electrical shock, do not open the cabinet. Refer servicing to qualified personnel only.

THIS APPARATUS MUST BE EARTHED.

To disconnect the main power, unplug the AC IN connector.

This symbol indicates the equipotential terminal which brings the various parts of a system to the same potential.

For the 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.

For the customers in Canada

This unit has been certified according to Standard CSA C22.2 No.601.1.

For the customers in the U.S.A. and Canada

Both the UP-990AD and the UP-970AD Hybrid Graphic Printers are Non-Patient Equipment.

These units cannot be used in the vicinity of patients.

* Patient Vicinity

.83m

R1

(6

feet)

 

 

When you use this product connected to 240V single phase, be sure to connect this product to a center tapped circuit.

Important safeguards/notices for use in the medical environments

1.All the equipments connected to this unit shall be certified according to Standard IEC60601-1, IEC60950-1, IEC60065 or other IEC/ISO Standards applicable to the equipments.

2.When this unit is used together with other equipment in the patient area*, the equipment shall be either powered by an isolation transformer or connected via an additional protective earth terminal to system ground unless it is certified according to Standard IEC60601-1.

*Patient Area

.5m R1

3.The leakage current could increase when connected to other equipment.

2