GTD9X1003-WWWVV-TW Desktop/External ICT / ITE / Medical Power Supply/Class 2/Household Power Supply Datasheet

GTD9X1003-WWWVV-TW, ICT / ITE / Medical Power Supply/Class 2/Household Power Supply,  60601-1-4th Ed. , Desktop/External, DC-DC, , Input Rating: 12-36V, , Output Rating: 100 Watts, Power rating with convection cooling (W) , 12-54V in 0.1V increments, Approvals: China RoHS; Double Insulation; PSE; RoHS; UKCA; Ukraine; VCCI; WEEE; GTD9X1003-WWWVV-TW, ICT / ITE / Medical Power Supply/Class 2/Household Power Supply,  60601-1-4th Ed. , Desktop/External, DC-DC, , Input Rating: 12-36V, , Output Rating: 100 Watts, Power rating with convection cooling (W) , 12-54V in 0.1V increments, Approvals: China RoHS; Double Insulation; PSE; RoHS; UKCA; Ukraine; VCCI; WEEE;GTD9X1003-WWWVV-TW, ICT / ITE / Medical Power Supply/Class 2/Household Power Supply, 60601-1-4th Ed. , Desktop/External, DC-DC, , Input Rating: 12-36V, , Output Rating: 100 Watts, Power rating with convection cooling (W) , 12-54V in 0.1V increments, Approvals: China RoHS; Double Insulation; PSE; RoHS; UKCA; Ukraine; VCCI; WEEE; GTD9X1003-WWWVV-TW, ICT / ITE / Medical Power Supply/Class 2/Household Power Supply, 60601-1-4th Ed. , Desktop/External, DC-DC, , Input Rating: 12-36V, , Output Rating: 100 Watts, Power rating with convection cooling (W) , 12-54V in 0.1V increments, Approvals: China RoHS; Double Insulation; PSE; RoHS; UKCA; Ukraine; VCCI; WEEE;
Model NumberGTD9X1003-WWWVV-TW
CE EC-Declaration for Medical
CE EC-Declaration for Industrial/Commercial/ITE
CE EC-Declaration for HouseholdContact GlobTek for more information
UKCA-Declaration for Medical
UKCA-Declaration for Industrial/Commercial/ITE
UKCA-Declaration for HouseholdContact GlobTek for more information
Morocco SDoC Declaration
RoHS/RoHS3 Declaration
Prop 65 Statement
REACH Declaration
Conflict Minerals Declaration
Model Parameters
CategoryICT / ITE / Medical Power Supply/Class 2/Household Power Supply
Input Voltage Range (V)12-36V
Max Input Current (A)12.0A
Max Output Power Rating (W)100
Output Voltage Range (V)12-54
Ingress ProtectionIP43
Size (mm)149.4 x 62.6 x 33.5

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Rating Table
Preferred ratings shown below.
Custom output voltages available in 0.1V increment from the minimum voltage listed to the maximum voltage listed; contact sales.
Model Number (Final ordering #/Part No to be defined)Voltage (V)Current (A)Power (W)RFQ
* (Final ordering #/Part No to be defined)



  • 2 x MOPP medical isolation
  • EMS-ready per IEC60601-1-12
  • Wide "universal" DC input range
  • 120W short-term power capability (optional)
  • Shock & vibration in accordance with IEC60601-1-12 (EMS)


Input Voltage Range:12 - 36VDC (nameplate, nominal)
10.2 - 39.6VDC (rated, -15% / +10%)

Plus short-term capability between 9.0 - 10.2V. (Duration is limited by temperature rise.)
Input Current:9.5A (typ.) @ 12VDC
12.0A (max.) @ 10.2VDC
No Load Input Power:< 0.5W
Efficiency:87% @ 12VDC, 90% @ 24VDC typ., at a "typical" 60W usage scenario


Turn-on Delay:< 2 seconds
Output Regulation:+1.5% / -4% max. (measured at the output connector)
Line Regulation:± 0.1 % typ.  (measured at the output connector)
Ripple:1% max. (using a 10µF low-ESR electrolytic cap + 0.1µF ceramic cap, measured @ 20MHz BW, at the output connector)
Transient Response (Step Load):10% max. deviation, 2ms max. recovery time (with 100W load step)
Transient Response
(Load Dump):
5% max. deviation, 100ms max. recovery time (with 100W load dump)


Input Protection:Input line fusing (high-breaking capacity)
Reverse polarity protection (up to -36VDC)
Input Under-Voltage Protection:Shut down @ 7.4V (typ.), Restore @ 9.0V (max.)
Output Over-Voltage Protection:110 - 130%, Latching, cycle DC input voltage to reset
Output Over-Current Protection:110 - 150%, Auto-recovery
Output Short-Circuit Protection:Auto-recovery
Over-Temperature Protection:Latching, cycle DC input voltage to reset


MTBF:> 1,500,000 hours @ 25°C ambient (Telcordia SR-332, Issue 3)
Operating Temperature:-10°C to 40°C (100W)
Check derating curve for T > 40°C.
Storage Temperature:-40°C to 80°C
Humidity:0% to 95% relative humidity, non-condensing
Cooling:Natural convection
Shock:End use handling: Half-sine, <3ms duration, 1.65m/s, 3 shocks per face
Transportation simulation: Trapezoid, 60G acceleration, 5.75m/sec, 3 shocks per face
General shock: Half-sine, 100G acceleration, 6ms duration, 3 shocks per face
Vibration:IEC60601-1-12, Section 10.1.3, Clause B
Bump:EN1789, Clause 6.4.1
Drop:EN1789, Clause 6.4.2
Ingress Protection:IP43
RoHS:Complies with EU 2015/863 and China SJ/T 11363-2006


Compliant Standards:General medical: IEC60601-1
Emergency medical services (EMS): IEC60601-1-12
Information & communications technologies (ICT): IEC62368-1
Dielectric Withstand Voltage (Hi-Pot):4300VDC from input to output,  1 minute
4300VDC from input to case, 1 minute
500VAC from output to case, 1 minute
Output Leakage Current:NC: 8µA max.
SFC: 40µA max.
Means of Protection (Primary-to-Secondary):2 x MOPP
Protection Class:Class II (reinforced insulation)


Compliant Standards:Medical: IEC60601-1-2
Aftermarket automotive: EN50498
Conducted Emissions:CISPR25, Class 3
(measured with resistive load)
Radiated Emissions:CISPR25, Class 3
(measured with resistive load)
Electrical Transient Conduction Along Supply Lines:ISO7637-2 (Test conditions for  12V nom.  / 24V nom. systems, respectively)
   Test Pulse 1:  - 100V / -600V (5,000 pulses)
   Test Pulse 2a: + 50V / + 50V (5,000 pulses)
   Test Pulse 2b: + 10V / + 20V (10 pulses)
   Test Pulse 3a: -150V / - 200V (1 hour)
   Test Pulse 3b: +100V / + 200V (1 hour)
   Test Pulse 4: -6V / -12V (1 pulse)

ISO16750-2 Load Dump:
   12V nom. system: Test Pulse B : Us* = 35V, Ri = 2Ω, td = 400ms
   24V nom. system: Test Pulse B:  Us* = 65V, Ri = 2Ω, td = 350ms
Electrostatic Discharge (ESD) Immunity:EN61000-4-2, 10KV contact discharge, 18KV air discharge, Criterion A
Radiated RF Immunity:EN61000-4-3, 20V/m @ 80MHz - 2.7GHz, 80% 1KHz AM, 80% 5Hz AM, Criterion A
Conducted RF Immunity:EN61000-4-6, 3VRMS & 6VRMS (ISM & Amateur bands), 80% 1KHz AM, Criterion A


Housing:High impact plastic, 94V0 polycarbonate, non-vented
Markings:Adhesive backed label or laser engraving
Derating CurveUser-added image
Qty (ea.)/Carton60
Individual Box/Gift Box Size (mm)Egg Crate
Individual Box/Gift Box Color
Master Carton Size (mm)480 x 450 x 205
Gross Weight (kg)15.2
Label Width (mm)50.0
Label Height (mm)110.0
Input Configuration
Output Configuration
Common output connector options:
Click to add to your request.
L Type (Coaxial 5.5x2.5mm plug)
C Type (Coaxial 5.5x2.1mm plug)
K Type (Coaxial 3.5x1.3mm plug)
LL Type (5.5x2.5mm Locking 760k type)
CL Type (5.5x2.1mm Locking S761k type)
Magnetic Connector
L Type (Coaxial 5.5x2.5mm plug)C Type (Coaxial 5.5x2.1mm plug)K Type (Coaxial 3.5x1.3mm plug)LL Type (5.5x2.5mm Locking 760k type)CL Type (5.5x2.1mm Locking S761k type)Magnetic Connector
YL3 Type (KPPX-3P)
YL4 Type (KPPX-4P)
EJ1/2/3/4/5 (EIAJ RC-5320A type connectors)
MSB Type (Micro USB)
Custom design
YL3 Type (KPPX-3P)YL4 Type (KPPX-4P)EJ1/2/3/4/5 (EIAJ RC-5320A type connectors)MSB Type (Micro USB)Inquire for custom design

For a comprehensive list of options, click here

Contact GlobTek for your specific requirements or custom solutions.


Below follows a link to the latest regulatory certifications and marks for this specific product. National standards as well as certification schemes are constantly changing and so is the set of certification marks and symbols applicable to this product. Various standards, marks and symbols, and certificates are subject to change at any time without notice.

Additional standards or unique country certifications are available upon request. Please contact Globtek to request a quotation.

Medical 4th Ed.EN/IEC 60601-1-2, 4th Edition (Please visit EMC reports for further info)
User-added imageCHINA SJ/T 11364-2014, China RoHS Chart:
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User-added imageIndoor Use Only - Mark is on the label or Molded in the case
User-added imageJAPAN TUV R-PSE, Cert. No. JD 50469658, to J62368-1(H30) , J55032(H29),J3000(H25)[15V or less]. Please reference the following website for guidelines on PSE regulations:
RoHSSpecifications of directive 2011/65/EU Annex VI (ROHS-2) with amendment 2015/863-EU (ROHS-3)
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UKCA Certification
User-added imageUkraine UKRSepro (Document:
User-added imageJapan: Voluntary Control Council for Interference (VCCI)
 User-added imageWEEE: Complies with EU 2012/19/EU ( Mark is on the label or Molded in the case
Popular Products (Stock items)
SKUVolts OutCurrent Out (Amps)ConnectorRFQSample Request
What is an IEC 60601-1 medical grade rated power supply AC adapter?

An IEC 60601-1-2 medical grade rated power supply AC adapter converts input line voltage from the wall to a lower voltage, typically DC, which is used to operate and end use piece of medical equipment. IEC 60601-1-2 medical grade power supply AC adapters are typically housed in a plastic enclosure and are available with both 2 and 3 prong input options. power supplies are also available as open frame for use inside of medical equipment. These AC to DC converters are designed in accordance with international medical standards and provide for compliance with certain aspects of them which differs from generic information and communication technology equipment power supplies.

Why is my medical grade IEC 60601-1 power supply certified to IEC 60601-1 3rd Edition while the latest standard is IEC 60601-1 4th Edition?
IEC 60601-1 has different sections in specifications for safety and EMI/EMC. The latest revision of the safety portion of  IEC 60601-1 is 3rd Edition while for EMI/EMC the latest revision is 60601-1-2, 4th Ed. 

What is the effective date of 60601-1-2, 4th Ed?
60601-1-2, 4th Ed. was effective on December 31, 2018.

What's the difference between an IEC 60950-1 and IEC 60601-1 medical grade rated power supply?

IEC 60950-1 and IEC 60601-1-2 power supplies are both AC to DC converters and may be either internal or external but are designed to different specifications to match the end system specifications. While the basic performance behaviors are similar such as input and output voltages and mechanical configurations, there are many differences as well. Some of the key differences are that medical IEC 60601 medical grade AC to DC adapters are able to withstand a higher dielectric withstand voltage and must have lower leakage current.  There are many other differences and also considerations to consider depending on the end use application.  

What MOOP and MOPP?
Medical devices must incorporate one or more Means of Protection (MOPs) to isolate patients and operators from the risks of electrocution. A Means of Protection (MOPs)  can be safety insulation, a protective earth, a defined creepage distance, or an air gap or other protective impedance. These can be used in various combinations. IEC 60601-1 3rd edition differentiates between the risk to patients and the risk to operators. A MOP can therefore be classified as Means of Patient Protection (MOPP) or a Means of Operator Protection (MOOP). The main difference between one MOOP and one MOPP is primarily one of permissible creepage distance. Both requirements are satisfied using Basic insulation. To achieve 2 x MOPP qualification the isolation test is particularly demanding at 4000 Vac and the creepage distance of 8mm is twice that required for one MOPP. 

What is a BF and CF rated an IEC 60601-1-2 medical grade rated power supply AC adapter and what is the difference?

Medical grade power supplies and AC to DC adapters are categorized into one of three applied parts types: body type (B), body floating type (BF), and cardiac floating type (CF). These applied parts require specific attributes such as isolation voltage, creepage and leakage current. Floating refers to an ungrounded power supply, Class II, that is not referenced to another output and is fully isolated. Type B refers to devices that operate within the patient's vicinity, as described in IEC 60601-1 as six feet around a patient's chair or bed and do not touch the patient electronically and are grounded. These devices include operating room lighting, hospital carts and beds, automated dispensers of medication and supplies, and diagnostic equipment like x-ray machines. Type BF devices deliver electrical energy signals to or from the patient such as electrosurgical devices, endoscopes, and electrical vital sign monitors like thermometers. Type CF devices are similar to BF, except they supply power to devices connected to the heart, such as a defibrillator, external pacemaker or intracardiac ECG electrodes and Type CF requires a higher degree of protection against electrical shock than BF types.  

Is level VI efficiency required for power over Ethernet?

According to the department of energy of the United States,  An EPS may be considered a Class A EPS if it connects to the end-use application using any type of electrical connection, cable, cord, or other wiring, including both removable and hard-wired connections. An Ethernet cable would meet these criteria, so an EPS that connects to the end-use product via an Ethernet cable would still be considered a Class A EPS and would be subject to the applicable energy conservation standards if it meets the other  five criteria of a Class A EPS. In general all power over ethernet power supply adapters meet all criteria and are required to be level VI efficiency.

What is a IEC 62368-1:2018 power supply?

IEC 62368-1:2018 is applicable to the safety of electrical and electronic equipment within the field of audio, video, information and communication technology, and business and office machines with a rated voltage not exceeding 600 V. This is a product safety standard that classifies energy sources, prescribes safeguards against those energy sources, and provides guidance on the application of, and requirements for, those safeguards. The prescribed safeguards are intended to reduce the likelihood of pain, injury and, in the case of fire, property damage. An IEC 62368-1 rated AC to DC converter or power supply is a power supply that has been tested to and certified to comply with the said standard.

Did IEC 62368-1 power supplies replace IEC60950-1 power supplies?

On December 20, 2020 the safety standards that historically have applied to information technology equipment and audio video equipment, IEC 60065 and IEC 60950-1,transition to IEC 62368-1. In North America ETL and UL 60950-1 certifications will continue to stay valid and may continue to be used until further notice. 

What is the difference between an IEC 62368-1 and a IEC 60950-1 power supply?

While the structure and contents of the standards are very different in general most products that previously complied with IEC 60950-1 comply with the latest standard IEC 62368-1 with little or no modification.

Will my IEC60950-1 power supply remain available?

GlobTek will continue to manufacture and supply IEC 60950-1 power supplies indefinitely until further notice.

What is the The Unique Device Identification (UDI) for my GlobTek medical grade power supply?

The Unique Device Identification (UDI) as required by the Food and Drug Administration Amendments Act of 2007 and EU Medical Device Regulation (MDR) is required for registered medical devices. While GlobTek medical grade power supplies carry full medical certifications they're actually not considered medical devices themselves but a component of such. And therefore do not have registration with the Food and Drug Administration Amendments Act of 2007 and EU Medical Device Regulation (MDR) and therefore so not carry a The Unique Device Identification (UDI).
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