Adaptive USB PD Power Supply/ Quick Charge Charger for Medical Grade and ITE/ICT applications for USB PD 2.0 and USB PD 3.0 Applications T2
|Communication formats supported: USB Power Delivery (PD) 2.0/3.0, Quick Charge™ 2.0/3.0, Quick Charge™ 4.0/4.0+ with up to 7 voltages and VDM options available. Fully globally certified for Medical 60601-1, ICT 62368 Communication formats supported: USB Power Delivery (PD) 2.0/3.0, Quick Charge™ 2.0/3.0, Quick Charge™ 4.0/4.0+ with up to 7 voltages and VDM options available. Fully globally certified for Medical 60601-1, ICT 62368|
|CE EC-Declaration for Medical||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000PGI8DEAX|
|CE EC-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000PGI8DEAX|
|CE EC-Declaration for Household||Contact GlobTek for more information|
|UKCA-Declaration for Medical||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000PGI8DEAX|
|UKCA-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000PGI8DEAX|
|UKCA-Declaration for Household||Contact GlobTek for more information|
|Morocco SDoC Declaration||https://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0O0c00000PGI8DEAX|
|Prop 65 Statement||https://en.globtek.com/prop-65-statement.pdf|
|Conflict Minerals Declaration||https://www.globtek.com/pdf/conflict-minerals.pdf|
|Technology||USB Adaptive Power Supply AC Adaptor|
|Category||USB Power Delivery (PD) Source, ICT/ITE/Medical|
|Input Voltage Range (V)||100-240V~, 50-60Hz|
|Max Input Current (A)||1.5A|
|Max Output Power Rating (W)||60|
|Output Voltage Range (V)||3.6-20|
|Efficiency||USA DOE Level VI / Eco-design Directive 2009/125/EC, (EU) 2019/1782|
Drawing above is model with output cord
Drawing above is model with integrated USBC connector (suffix -RA)
|3D File Download||https://www.globtek.com/dl/GTM96605-T2.igs|
* (Final ordering #/Part No to be defined)
USB Power Delivery Capabilities
Qualcomm Quick Charge™ Capabilities
Prevention of Unauthorized Use
Non-standard - Contact GlobTek
† 15.1V PDO is standard on units with date codes after Sept-10-2019.
|Individual Box/Gift Box Size (mm)||Egg Crate|
|Individual Box/Gift Box Color|
|Master Carton Size (mm)||455 x 430 x 320|
|Gross Weight (kg)||15.6|
|Label Width (mm)|
|Label Height (mm)|
|Description||IEC 60320/C8 AC Inlet connector, Class II, Non-Earth Ground (aka "Figure-8")|
|Common output connector options:|
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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.
|Popular Products (Stock items)|
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 Level VI Efficiency?
The numerals I to VI are an International Efficiency Marking Protocol which allows manufacturers to designate the efficiency performance of a product. This performance is based on the measurement of the operating energy efficiency and no-load power consumption of external power supplies or AC DC adapters tested at different load levels. The no-load power consumption refers to the amount of power that an external power supply draws even when the application is turned off or disconnected.
Is Level VI Efficiency required?
Level VI efficiency is mandated in certain countries and regions for certain products or certain applications.
What is the Eco-design Directive 2009/125/EC?
The Eco-design directive put into law in Europe the latest requirements for energy efficiency and conservation for AC DC adapters and external power supplies.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).