File E116994 Project 96SC12407 Issued: November 26, 1996 Revised: October 19, 2006 REPORT ON COMPONENT - POWER SUPPLIES, MEDICAL AND DENTAL EQUIPMENT SL Power Electronics Corp. Ventura, California Copyright © 1996 Underwriters Laboratories Inc. Underwriters Laboratories Inc. authorizes the above-named company to reproduce this Report provided it is reproduced in its entirety. Underwriters Laboratories Inc. authorizes the above named company to reproduce that portion of this Report consisting of this Cover Page through Page 3. File E116994 Vol. 1 Sec. 47 and Report Page 1 Issued: Revised: 1996-11-26 2006-10-06 DESCRIPTION PRODUCT COVERED: Component - Switching Power Supplies, Medical and Dental, Models GLM75 followed by suffixes A, A-103, B, C, D, E, F, H, H-101, J, or P, may or may not be followed by -L , -C or –LC, and/or -V. May or may not be followed by an Optional “G”, which indicates compliance with RoHS. (RoHS compliance has not been evaluated by UL.) ELECTRICAL RATINGS: Input: Output: 100-240 V ac, 50/60 Hz, 3.1 A. Maximum Continuous Power, total of all outputs at ambient of 50 °C. Output #1 MODEL GLM75A GLM75A-103 GLM75B GLM75C GLM75D GLM75E GLM75F GLM75H GLM75H-101 GLM75J GLM75P +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V +5.1 V Standard & -L option 26 CFM 0 CFM 110 Watts 75 Watts Output #2 Note 2 Note 3 8A 8A 8A 8A 8A 8A 8A 8A 8A 8A 8A 10 A 10 A 10 A 10 A 10 A 10 A 10 A 10 A 10 A 10 A 10 A +12 V +12 V +12 V +12 V +24 V +24 V +15 V +15 V +15 V +12 V +24 V Note 2 Note 3 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 4.0 A 3.0 A 3.0 A 3.0 A 3.0 A 2.5 A 2.5 A 3.0 A 3.0 A 3.0 A 3.0 A 4.0 A With Chassis/Cover (Note 26 CFM 0 CFM 110 Watts 65 Watts 5) Output #3 Output #4 Note 2 Note 3 Note 2 Note 3 -12 V 1.0 A 1.0 A -5 V -15 V -12 V -15 V -5 V -15 V -15 V -12 V -12 V 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 1.0 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.5 A 2.0 A 2.5 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A 3.0 A +12 V -12 V +12 V +15 V +12 V +15 V -15 V +15 V +16 V 5V +12 V Notes: 1. Model may be followed by –L for chassis bracket, –C or –LC for chassis/cover, or –V for Voltage Adj. Pot (+5.1V). 2. Maximum ratings for 0 CFM airflow without chassis/cover. 3. Maximum ratings for 26 CFM airflow. 4. Maximum Operating Relative Humidity 96 %, no condensation. 5. Contact Condor Technical Support for airflow requirements when using chassis/cover option. 6. Storage: -40 to +85 °C. Units should be allowed to warmup under non-condensing conditions before application of power. File E116994 Vol. 1 Sec. 47 and Report Page 2 Issued: Revised: 1996-11-26 2006-10-06 ENGINEERING CONSIDERATIONS (NOT FOR FIELD REPRESENTATIVE'S USE): For use in product where the acceptability of the combination is determined by Underwriters Laboratories Inc. This product was evaluated to the Standard For Medical Electrical Equipment, Part 1: General Requirements for Safety, UL 60601-1. An insulation diagram is provided as ILL. 3. Condition of Acceptability - When installed in the end-use equipment, the following are among the considerations to be made: 1. This component has been judged on the basis of the required spacings in the Standards for Medical Electrical Equipment, Part 1: General Requirements for Safety, UL 60601-1, which covers the end use product for which the component is designed. 2. The component shall be installed in compliance with the enclosure, mounting, spacing, casualty markings and segregation requirements of the end-use application. 3. Consideration should be given to measuring the temperature on power electronic components and transformer windings when the power supply is installed in the end-use equipment. 4. The input/output connectors are not acceptable for field connections, they are only intended for connection to mating connectors of internal wiring inside the end-use machine. The output circuits have not been evaluated for direct patient connection (Type B, BF or CF). 5. The component should be properly bonded to ground in the end-use equipment. File E116994 Vol. 1 Sec. 47 and Report Page 3 Issued: Revised: 1996-11-26 2003-02-18 6.* The Temperature Tests were as performed in a raised ambient of 50°C., 7. The main isolation transformer, T3, complies with Class 155 limits. 8. Leakage current testing should be repeated in the end product application. 9. The power supply was evaluated as Reinforced insulation between primary and secondary; basic insulation between primary to ground and secondary to ground. 10. This power supply has been evaluated as Class I, continuous operation, ordinary equipment and has not been evaluated for use in the presence of a flammable anaesthetic mixture with air, oxygen, or nitrous oxide. 11. Fusing in the end-product shall be considered since primary fusing of both sides on the mains supply line was not provided (3.15 A fuse provided on input line side). 12. Under normal and single fault conditions, the outputs do not exceed 25 V ac or 60 V dc.