Linear Medical Safety Certificates

File E116994
Project 90SC14984
1990-11-07
REPORT
ON
COMPONENT - POWER SUPPLIES,
MEDICAL AND DENTAL EQUIPMENT
CONDOR D C POWER SUPPLIES INC.
Oxnard, California
Copyright
1990 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. 15
and Report
Page 1
Issued:
Revised:
1990-11-07
2004-06-02
DESCRIPTION
PRODUCT COVERED:
COMPONENT – Medical Linear Power Supplies, Models MB5-3-OVP-A, MB121.7-A, MB15-1.5-A, MB24-1.2-A, MB28-1-A, MC5-6-OVP-A, MC12-3.4-A, MC15-3-A,
MC24-2.4.A, MC28-2-A, MAA15-0.8-A, MAA512-A, MAA524-A, MBB15-1.5-A, MBB512-A,
MBB524-A, MTAA-16W-A, MBAA-40W-A, MCP1249 and MCP1799.
ELECTRICAL RATINGS:
Input:
100/120/215/230-240 V ac, 50/60 Hz,
Input currents vary by model. See table below.
Model #
MB5-3-OVP-A
MB12-1.7-A
MB15-1.5.A
MB24-1.2-A
MB28-1-A
MC5-6-OVP-A
MC12-3.4-A
MC15-3-A
MC24-2.4-A
MC28-2-A
MAA15-0.8-A
MAA512-A
MAA524-A
MBB15-1.5-A
MBB512-A
MBB524-A
MTAA-16W-A
MBAA-40W-A
MCP1249
MCP1799
Input Currents
100 V ac
120 V ac
0.75
0.75
0.75
0.8
0.8
1.1
1.2
1.3
1.4
1.4
0.77
0.75
0.7
0.65
1.2
1.2
0.7
1.3
1.4
0.75
0.6
0.6
0.75
0.65
0.75
0.9
1.0
1.1
1.2
1.2
0.65
0.75
0.6
0.56
1.0
1.1
0.6
1.1
1.2
0.6
215 V ac
0.4
0.4
0.4
0.4
0.4
0.5
0.6
0.6
0.7
0.7
0.35
0.4
0.3
0.31
0.6
0.6
0.3
0.6
0.2
0.4
230-240 V ac
0.4
0.4
0.4
0.4
0.4
0.5
0.5
0.6
0.6
0.6
0.33
0.4
0.3
0.28
0.5
0.5
0.3
0.6
0.6
0.4
File E116994
Output:
Vol. 1
Volts
MB5-3-OVP-A
MB12-1.7-A
MB15-1.5.A
MB24-1.2-A
MB28-1-A
MC5-6-OVP-A
MC12-3.4-A
MC15-3-A
MC24-2.4-A
MC28-2-A
MAA15-0.8-A
MAA512-A
9
MAA524-A
18
MBB15-1.5-A
MBB512-A
9
MBB524-A
18
MTAA-16W-A
±12
MCP1249
MCP1799
Page 2
Issued:
Revised:
1990-11-07
2004-06-02
Maximum output power for each unit is defined below.
Output power is derated 10% for 50Hz operation.
Model
MBAA-40W-A
Sec. 15
and Report
5
12
15
24
28
5
12
15
24
28
±15
±12
5
to 15
5
TO 24
15
5
to 15
5
TO 24
5
to ±15
5
±15
±12
26
6.5
Amps, 60 Hz
3.0
1.7
1.5
1.2
1.0
6.0
3.4
3.0
2.4
2.0
1.0
0.8
2.0
0.5
2.0
0.3
1.5
3.0
1.25
3.0
0.8
2.0
0.4
3.0
0.8
1.0
2.0
1.4
Amps, 50 Hz
Max Watts
2.7
1.53
1.35
1.08
0.9
5.4
3.06
2.7
2.16
1.8
0.9
0.72
1.8
0.45
1.8
.27
1.35
2.7
1.125
2.7
0.72
1.8
0.36
2.7
0.72
0.9
1.8
1.26
15.0
20.4
22.5
28.8
28.0
30.0
40.8
45.0
57.6
56.0
30.0
19.2
17.5
--17.2
--22.5
33.75
--29.2
--22.0
--39.0
----52.0
9.1
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 First Edition of the Standard For
Medical Electrical Equipment, Part 1: General Requirements for Safety, UL
60601-1. An insulation diagram is provided as Ill. 1, the manufacturer's
installation instructions is provided as Ills. 2 and the transformer
information diagram is provided as Ills. 3 and 4.
File E116994
Vol. 1
Sec. 15
and Report
Page 3
Issued:
Revised:
1990-11-07
2004-06-02
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 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.
Leakage current testing should be repeated in the end product
application.
4.
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.
5.
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.
6.
The Temperature Test was performed in a raised ambient of 50°C.
7.
The component should be properly bonded to ground in the end-use
equipment.
8.
The output circuits have not been evaluated for direct patient
connection (Type B, BF or CF).
9.
The main isolation transformer, T1, complies with Class B (130°°C)
limits, except for MB24-1.2-A, MB28-1-A, MAA15-0.8-A, MTAA-16W-A,
MC24-2.4-A, and MCP1799, which comply with Class F (155°°C) limits.
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 anaesthetic mixture with air, oxygen, or
nitrous oxide.
12.
Double fusing in the end-product should be considered since primary
fusing of both sides on the mains supply lines was not provided.
File E116994
Project 90SC13193
1990-11-29
REPORT
ON
COMPONENT - POWER SUPPLIES,
MEDICAL AND DENTAL EQUIPMENT
CONDOR D C POWER SUPPLIES INC.
Oxnard, California
Copyright  1990 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. 16
and Report
Page 1
Issued:
1990-11-29
DESCRIPTION
PRODUCT COVERED:
COMPONENT – Medical Linear Power Supplies, Models MD5-12/OVP-A, MD126.8-A, MD15-6-A, MS24-4.8-A, MD28-4-A, MCC15-3-A, MCC512-A, MCC524-A, MCAA60W-A, MCBB-75W-A, MCP1279.
ELECTRICAL RATINGS:
Input:
100/120/215/230-240 V ac, 50/60 Hz,
Input currents vary by model. See table below.
Model #
MD5-12/OVP-A
MD12-6.8-A
MD15-6-A
MD24-4.8-A
MD28-4-A
MCC15-3-A
MCC512-A
MCC524-A
MCAA-60W-A
MCBB-75W-A
MCP1279
Input Currents
100 V ac
120 V ac
215 V ac
230-240 V ac
2.3
2.8
2.8
2.8
2.5
3.0
2.5
2.4
3.0
2.3
2.5
1.9
2.4
2.4
2.4
2.1
2.8
2.2
2.1
2.8
2.0
2.1
1.0
1.3
1.3
1.3
1.2
1.5
1.2
1.2
1.5
1.1
1.2
1.0
1.2
1.2
1.2
1.1
1.4
1.1
1.0
1.4
1.0
1.1
File E116994
Output:
Model
MD5-12/OVP-A
MD12-6.8-A
MD15-6-A
MD24-4.8-A
MD28-4-A
MCC15-3-A
MCC512-A
MCC524-A
MCAA-60W-A
MCBB-75W-A
MCP1279
Vol. 1
Sec. 16
and Report
Page 2
Issued:
1990-11-29
Maximum output power for each unit is defined below.
Output power is derated 10% for 50 Hz operation.
Volts
5
12
15
24
28
±15
±12
5
9 TO 15
5
18 TO 24
5
±15
±12
5
±15
±12
28
Amps, 60 Hz
12.0
6.8
6.0
4.8
4.0
3.0
3.4
6.0
2.5
6.0
2.0
6.0
0.8
1.0
6.0
1.5
1.71
4.0
Amps, 50 Hz
Max Watts
10.8
6.12
5.4
4.32
3.6
2.7
3.06
5.4
2.25
5.4
1.8
5.4
0.72
0.9
5.4
1.35
1.54
3.6
60
81.6
90.0
115.2
112.0
90
81.6
67.5
--78.0
--54.0
----74.5
----112
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 Second Edition of the Standard For
Medical Electrical Equipment, Part 1: General Requirements for Safety, UL
2601-1. An insulation diagram is provided as Ill. 1, the manufacturer's
installation instructions is provided as Ills. 2 and the transformer
information diagram is provided as Ills. 3.
Conditions 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 Second Edition of the Standards for Medical Electrical
Equipment, Part 1: General Requirements for Safety, UL 2601-1, which
covers the end use product for which the component is designed.
File E116994
Vol. 1
Sec. 16
and Report
Page 3
Issued:
1990-11-29
2.
The component shall be installed in compliance with the enclosure,
mounting, spacing, casualty, markings and segregation requirements of
the end-use application.
3.
Leakage current testing should be repeated in the end product
application.
4.
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.
5.
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.
6.
The Temperature Test was performed in a raised ambient of 50°C.
7.
The component should be properly bonded to ground in the end-use
equipment.
8.
The output circuits have not been evaluated for direct patient
connection (Type B, BF or CF).
9.
The main isolation transformer, T1, complies with Class 130 limits,
except for MD24-4.8, MD28-4-A AND MCP1279 which comply with Class 155
limits.
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 anaesthetic mixture with air, oxygen, or
nitrous oxide.
12.
Double fusing in the end-product should be considered since primary
fusing of both sides on the mains supply lines was not provided.
Certificate of Compliance
Certificate:
1231873 (LR 46516C)
Master Contract:
150684
Project:
1566321
Date Issued:
2004/06/14
Issued to:
Condor D.C. Power Supplies Inc.
2311 Statham Pky
Oxnard, California 93033
USA
Attention: Mr. Dave Hemphill
The products listed below are eligible to bear the CSA Mark shown
with adjacent indicators 'C' and 'US'
Issued by:
Mohamed Omran, P. Eng.
Authorized by: Shane Stevenson, Product
Group Manager
PRODUCTS
CLASS 5311 20
CLASS 5311 96
- POWER SUPPLIES - Component Type - For Use in Medical Equipment
- POWER SUPPLIES - Component Acceptance - Certified to US Standards
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0))!1) +))1) /-22*
The 'C' and 'US' indicators adjacent to the CSA Mark signify that the product has been evaluated to the applicable CSA and ANSI/UL Standards, for use in Canada and the
U.S., respectively. This 'US' indicator includes products eligible to bear the 'NRTL' indicator. NRTL, i.e. National Recognized Testing Laboratory, is a designation granted
by the U.S. Occupational Safety and Health Administration (OSHA) to laboratories which have been recognized to perform certification to U.S. Standards.
DQD 507 2003/01/31
Certificate:
1231873 (LR 46516C)
Master Contract:
150684
Project:
1566321
Date Issued:
2004/06/14
3 4 , 5 6 *
7(
89' & 6 '& 6 :/*
APPLICABLE REQUIREMENTS
/)7/) /* 7* !*2 8
89'
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9' ( <
=9' 6 6%
DQD 507 2003/01/31
Supplement to Certificate of Compliance
Certificate:
Master Contract:
1231873
150684
The products listed, including the latest revision described below, are eligible to be
marked in accordance with the referenced Certificate.
Product Certification History
Project
Date
Description
1566321
2004/06/14
Update Report 1231873 to Add New Model Designation MCP1799.
History
1231873
2001/08/07
Original Certification.