File E116994 Project 00SC14101 September 27, 2000 REPORT ON COMPONENT - POWER SUPPLIES, MEDICAL AND DENTAL EQUIPMENT Condor DC Power Supplies, Inc. Oxnard, California Copyright © 2000 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 4. File E116994 Vol. 1 Sec. 70 and Report Page 1 Issued: Revised: 2000-09-27 2005-12-14 DESCRIPTION PRODUCT COVERED: USR, CNR - COMPONENT, Switching Power Supply, Medical and Dental, Models GLD140A-102, GLD140H-101, GLD140X-C or -CF where X equals any alpha character A through Z which represents various output configurations, -C is a slotted cover option and –CF is a solid cover with fan option. . Models may be followed by suffix –XXX and/or G, where XXX may be any number from 001 thru 999 and suffix G indicates compliance to RoHS (RoHS compliance has not been evaluated by UL). ELECTRICAL RATINGS: Input: Output: 100-240 V ac, 50/60 Hz, 3.0 A. Output Output Output Output #1 #2 #3 #4 Volts 5 3.3 to 24 5 to 15 -15 to -12 Convection Amperes 16 max 10 max 4 max 0.75 max Airflow Amperes 20 max 12 max 5 max 1.2 max Power = 180 Watts maximum with cover/fan option or slotted Cover with a minimum of 150 LFM airflow. 140 Watts maximum with no airflow and no cover. Fan output is 12 V dc, 0.25 A GLD140H, GLD140H-101*: +5 V/6 A, +12 V/2.5 A, +15 V/2 A, -15 V/2A ª Maximum output power = 120W with Convection Cooling ENGINEERING CONSIDERATIONS (NOT FOR FIELD REPRESENTATIVE'S USE): USR – indicates investigation to the Standard for Medical Electrical Equipment, UL 60601-1, First Edition CNR – indicates investigation to Canadian Standard CSA C22.2 No. 601.1 For use in product where the acceptability of the combination is determined by Underwriters Laboratories Inc. File E116994 Vol. 1 Sec. 70 and Report Page 1A Issued: New: 2000-09-27 2005-05-31 ENGINEERING REFERENCES: Following Illustrations are provided for engineering references: Ill. Ill. Ill. Ill. 1 2 3 4 – – – – Isolation Diagram Installation Instruction Sheet PWB Trace Layout Transformer Construction Detail (T3 & T4) File E116994 Vol. 1 Sec. 70 and Report Page 2 Issued: Revised: 2000-09-27 2005-02-02 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 First Edition of the Standard 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. 5. The output circuits have not been evaluated for direct patient connection (Type B, BF or CF). 6. The component should be properly bonded to ground in the end-use equipment. 7. The Temperature Test was performed in a raised ambient of 50°C. 8. The isolation transformers, T3 and T4, complies with Class 155 limits. 9. Leakage current testing should be repeated in the end product application. 10. The power supply was evaluated as reinforced insulation between primary and secondary; basic insulation between primary to ground. 11. 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 anesthetic mixture with air, oxygen, or nitrous oxide. File E116994 Vol. 1 Sec. 70 and Report Page 3 Issued: 09-27-00 12. These power supplies have been evaluated for patient care equipment, but not patient connected. 13. Under normal and single fault conditions, the outputs do not exceed 25 V ac or 60 V dc. 14. The grounding trace on the pwb has not been evaluated as the Protective Earthing path for any metal parts accessible in the end product. However, the grounding path was subjected to the Earthing Test per Clause 18 (30 A for 2 minutes) with acceptable results. 15. This unit has not been evaluated for use with a slotted cover without airflow. File E116994 Vol. 1 Sec. 70 and Report Page 4 Issued: Revised: 2000-09-27 2005-12-14 CONSTRUCTION DETAILS: See Section General, Construction Details. Trace Layout - Field Representative to insure that the trace layout has not changed. See Ill. 3. Model Differences - All models are the same, except for output ratings and differences in secondary, low voltage circuitry. -C indicates slotted cover option, -CF indicates cover and fan option. GLD140H uses a 5 pin regulator for output #4, which requires a different PWB. New trace layout is added to Ill. 3. GLD140H-101 is identical to the model GLD140H-101 except it is provide with a slotted cover (item 23) GLD140A-102 is identical to model GLD140A except Line-to-Ground capacitors C3 & C4 value is changed from 1000 pF to 680 pF to reduce earth leakage current. Models followed by the suffix –XXX represents value added configurations that have no impact on safety. Models followed by the suffix G indicates compliance to RoHS (RoHS compliance has not been evaluated by UL).