Issue Date:
2012-02-09
Page 1 of 13
Report Reference #
E116994-A76-UL
UL TEST REPORT AND PROCEDURE
Standard:
Certification Type:
CCN:
Product:
Model:
ANSI/AAMI ES60601-1:2005, 3rd ed. (Medical Electrical Equipment Part 1: General Requirements for Basic Safety and Essential
Performance)
CAN/CSA-C22.2 No. 60601-1 (2008) (Medical Electrical Equipment Part 1: General Requirements for Basic Safety and Essential
Performance)
Component Recognition
QQHM2, QQHM8 (Power Supplies, Medical and Dental)
Power Supply
MINT1175AXXYYKZZ, MINT1175BXXYYKZZ, Where XX represents
the output voltage which may be any number from 12 to 56, YY
represents output connector which may be any two alphanumeric
digits, and ZZ represents non-safety related customer options and
RoHS statements which may be any two alphanumeric digits.
Input: 100-240V~, 50-60Hz, 3.0A
Rating:
Output:
With 200 LFM (linear feet per minute) forced air flow:
Main Output: 12Vdc/14.6A to 56Vdc/3.13A, Maximum 175W,
Fan Output: 12Vdc/0.4A
Without forced air flow:
Main Output: 12Vdc/10A to 56Vdc/2.15A, Maximum 120W,
Fan Output: 12Vdc/0.4A
Applicant Name and Address:
SL POWER ELECTRONICS CORP
BLDG A
6050 KING ST
VENTURA CA 93003
UNITED STATES
This is to certify that representative samples of the products covered by this Test Report have been investigated in accordance with the
above referenced Standards. The products have been found to comply with the requirements covering the category and the products are
judged to be eligible for Follow-Up Service under the indicated Test Procedure. The manufacturer is authorized to use the UL Mark on
such products which comply with this Test Report and any other applicable requirements of UL LLC ('UL') in accordance with the FollowUp Service Agreement. Only those products which properly bear the UL Mark are considered as being covered by UL's Follow-Up
Service under the indicated Test Procedure.
The applicant is authorized to reproduce the referenced Test Report provided it is reproduced in its entirety.
UL authorizes the applicant to reproduce the latest pages of the referenced Test Report consisting of the first page of the Specific
Technical Criteria through to the end of the Conditions of Acceptability.
Any information and documentation involving UL Mark services are provided on behalf of UL LLC (UL) or any authorized licensee of UL.
Prepared by:
Vincent Wan
Reviewed by: Richard Dolle
Copyright © 2012
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2012-02-09
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Report Reference #
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Supporting Documentation
The following documents located at the beginning of this Procedure supplement the requirements of this Test
Report:
A. Authorization - The Authorization page may include additional Factory Identification Code markings.
B. Generic Inspection Instructions i. Part AC details important information which may be applicable to products covered by this Procedure.
Products described in this Test Report must comply with any applicable items listed unless otherwise
stated in the body of this Test Report.
ii. Part AE details any requirements which may be applicable to all products covered by this Procedure.
Products described in this Test Report must comply with any applicable items listed unless otherwise
stated in the body of each Test Report.
iii. Part AF details the requirements for the UL Certification Mark which is not controlled by the technical
standard used to investigate these products. Products are permitted to bear only the Certification
Mark(s) corresponding to the countries for which it is certified, as indicated in each Test Report.
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2012-02-09
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Report Reference #
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Product Description
The MINT1175AWWXXYZZ series (Class I type), and MINT1175BWWXXYZZ series (Class II type) are
open-frame AC/DC power supplies, designed for building-in to an end-product used in a hospital or related
health care facility environment.
The power supplies output can be maximum 262 W with 175 LFM (linear feet per minute) forced air flow, or
de-rated to maximum of 120 W without forced air flow.
Model Differences
The MINT1175AWWXXYZZ series is Class I type; MINT1175BWWXXYZZ series is Class II type.
Class I construction installs a metal pillar for connecting to protective earth, which Class II construction does
not have. Class I construction installs a pair of 1500pF capacitors (C115, C116) from Mains lines to
protective earth, which Class II construction does not have.
All Models are identical in circuit with exception to the Mains Transformer T200 and minor secondary
components that allow for different output voltage ratings. There are four types of Mains Transformer T300 in
the series of power supplies, difference is number of turns on secndary winding N3, N4. Refer to Enclosure
4-06, 4-07.
Technical Considerations
Classification of installation and use : For building-in
Device type (component/sub-assembly/ equipment/ system) : Component, Power Supply
Intended use (Including type of patient, application location) : To supply regulated power to end
products.
Mode of operation : Continuous
Supply connection : Build-in
Accessories and detachable parts included : None
Other options include : None
The product was not investigated to the following standards or clauses:: Scope of Power Supply
evaluation defers the following clauses to the be determined as part of the end product: Clause 4.2
(Risk Management), Clause 7.5 (Safety Signs), Clause 7.9 (Accompanying Documents), Clause 9
(ME Hazard), Clause 10 (Radiation), Clause 14 (PEMS), Clause 16 (ME Systems).
The degree of protection against harmful ingress of water is:: IPX0 (All models).
The mode of operation is:: Continuous
The product is suitable for use in the presence of a flammable anesthetics mixture with air or oxygen
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2012-02-09
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or with nitrous oxide:: No
Software is relied upon for meeting safety requirements related to mechanical, fire and shock: No
Manufacturer’s Recommended Ambient: 50°C
The product is Classified only to the following hazards: Casualty, Fire, Shock
Power Supply was considered Overvoltage Category II (OVCII)
Engineering Conditions of Acceptability
For use only in or with complete equipment where the acceptability of the combination is determined by UL
LLC. When installed in an end-product, consideration must be given to the following:
Products install fuses on both line and neutral lines with breaking capacity of minimum 40A. In the
end-use application, the power source, which the products connect to, has to be reviewed for the
available short circuit current.
The products were tested on a 20A branch circuit, if use on a branch circuit greater than 20A,
additional tests may be necessary.
The component shall be installed in compliance with the Marking (clause 7) and Separation (clause
8) requirements of the end use application.
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. The end use
product shall ensure that the power supply is used within its ratings.
Transformer T200 provided with a Class F (155º) insulation system. Transformer T400 provided with
a Class B (130º) insulation system.
The end product should ensure that the requirements related to accompanying documents, clause
7.9, are met.
This power supply has been evaluated as 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. The output circuits have not been evaluated for direct patient connection (Type B, BF
or CF).
The available voltage for the secondary outputs does not exceed 25 Vac or 60 Vdc, under normal
and single fault conditions.
End product Risk Management Process to include consideration of requirements specific to the
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2012-02-09
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Power Supply.
End product Risk Management Process to consider the acceptability of risk for the following
components that were identified as High-Integrity Components: Fuses (F100, F101), Optocoupler
s(U201, U202, U601, U603, U501).
Single fault testing was conducted without dielectric breakdown, however end product Risk
Management Process to consider the need for simultaneous fault condition testing.
End product Risk Management Process to consider the need for different orientations of installation
during testing.
Humidity testing was conducted, however the end product Risk Management Process to determine
risk acceptability criteria.
Temperature Test was conducted without Test Corner. End product to determine the acceptability of
risk with respect to insulation’s resistance to heat, moisture, and dielectric strength per 8.8.4.
End product to determine the acceptability of risk in conjunction to the selection of components as it
pertains to the intended use, essential performance, transport, storage conditions as part of the
power supply.
Leakage current testing should be considered in the end product application.
The expected service life of this product is 5 years.
Models MINT1175BXXYKZZ are Class II products, the need for IEC symbol 60417-5172 should be
considered in the end use product.
For Class I configuration, Two MOPP is provided between primary and secondary; One MOPP is
provided between primary and earth (chassis), operational insulation provided between secondary
and earth.
For Class II configuration, Two MOPP is provided between primary and secondary.
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.
Limitation of Voltage/Energy test (8.4.3) was not conducted and should be considered in the end
product evaluation.
Input/output connectors are suitable for factory wiring only.
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2012-02-09
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Additional Information
The schematics for these models are kept in file at the CB Testing Laboratory mentioned in the first page of
this test report, and can be provided by the manufacturer upon request by NCB's/CBTL's.
When submitting this Test Report to other Certification Body, the manufacturer is responsible for providing
any additional information that the Body may need in order to issue its Mark, including testing for compliance
with the applicable collateral standards.
The Electrical and Nameplate Labels are representative of all models in the series.
Additional Standards
The product fulfills the requirements of: The product fulfills the requirements of: ANSI/AAMI ES60601-1
(2005 + C1:09 + A2:10) (Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and
Essential Performance) (includes Deviations for United States); CAN/CSA-C22.2 No. 60601-1 (2008)
(Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance)
(includes National Differences for Canada); EN 60601-1:2006 Medical electrical equipment - Part 1: General
requirements for basic safety and essential performance.
Markings and instructions
Clause Title
Marking or Instruction Details
Company identification
Classified or Recognized company's name, Trade name, Trademark or File
Model
Model number
Alternating current
Power Input
Amps, VA, or Watts
Fuses
Ratings (current and voltage) and type. (located adjacent to fuse OR as a diagram
inside enclosure)
Class II Mark
Only for Class II type models.
Special Instructions to UL Representative
N/A
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2012-02-09
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Production-Line Testing Requirements
Test Exemptions - The following models are exempt from the indicated test
Model
Grounding Continuity
Dielectric Voltage
Withstand
Patient Circuit Dielectric
Voltage Withstand
MINT1175BXXYYKZZ
Yes
No
N/A
Solid-State Component Test Exemptions - The following solid-state components may be disconnected
from the remainder of the circuitry during either Dielectric Voltage Withstand Test:
Component
N/A
Sample and Test Specifics for Follow-Up Tests at UL
The following tests shall be conducted in accordance with the Generic Inspection Instructions
Plastic Enclosure or Part
N/A
Test
Sample(s)
Test Specifics