60601-1 Medical DOE EPS 2.0 Level VI Power Supply / Charger, 5v, 3.2 A, with integral USB Jack, compliant with 2MOPP, 5000 Meters Elevation and 8 kV Contact/20kV Air Discharge ESD Protection
|GTM46161-16V.V-USB, ICT / ITE / Medical Power Supply, 60601-1-4th Ed. , Wall Plug-in, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Blade Options for Q Series Wall Plug-in Power Supplies, Output Rating: 16 Watts, Power rating with convection cooling (W) , 5-5.5V in 0.1V increments, Approvals: CCC; RCM; UL 1310; ETL; CB 60601-1; S-Mark IEC/EN 60601-1; S-Mark 60950; EAC; CB 62368; Conforms to 62368-1; LPS 62368; Morocco; LVD 60335; UKCA; Double Insulation; Ukraine; RoHS; China RoHS; Level VI; WEEE; ETL; CE; FCC; CAN ICES-3; PSE; IP20; CB 60950; GTM46161-16V.V-USB, ICT / ITE / Medical Power Supply, 60601-1-4th Ed. , Wall Plug-in, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Blade Options for Q Series Wall Plug-in Power Supplies, Output Rating: 16 Watts, Power rating with convection cooling (W) , 5-5.5V in 0.1V increments, Approvals: CCC; RCM; UL 1310; ETL; CB 60601-1; S-Mark IEC/EN 60601-1; S-Mark 60950; EAC; CB 62368; Conforms to 62368-1; LPS 62368; Morocco; LVD 60335; UKCA; Double Insulation; Ukraine; RoHS; China RoHS; Level VI; WEEE; ETL; CE; FCC; CAN ICES-3; PSE; IP20; CB 60950;|
|CE EC-Declaration for Medical||https://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000FiXUuEAN|
|CE EC-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000FiXUuEAN|
|CE EC-Declaration for Household||Contact GlobTek for more information|
|UKCA-Declaration for Medical||https://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000FiXUuEAN|
|UKCA-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000FiXUuEAN|
|UKCA-Declaration for Household||Contact GlobTek for more information|
|Morocco SDoC Declaration||https://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0Oa000000FiXUuEAN|
|Prop 65 Statement||https://en.globtek.com/prop-65-statement.pdf|
|Conflict Minerals Declaration||https://www.globtek.com/pdf/conflict-minerals.pdf|
|Technology||Regulated Switchmode AC-DC Power Supply AC Adaptor|
|Category||ICT / ITE / Medical Power Supply|
|Input Voltage Range (V)||100-240V~, 50-60 Hz|
|Max Input Current (A)||0.45A|
|Max Output Power Rating (W)||16|
|Output Voltage Range (V)||5-5.5|
|Efficiency||USA DOE Level VI / Eco-design Directive 2009/125/EC, (EU) 2019/1782 / Europe Code of Conduct on Energy Efficiency of External Power Supplies - Version 5|
|Ingress Protection||Indoor Use|
|3D File Download||https://www.globtek.com/file/dl/051515.rar|
* (Final ordering #/Part No to be defined)
|A) ELECTRICAL SPECIFICATIONS:|
1. Input Voltage: Specified 90-264 Vac, Nameplate rated 100-240 Vac
2. Input Frequency: Specified 47-63 Hz, Nameplate rated 50-60 Hz
3.Output Regulation: +/- 5% measured at the end of a 1.2 meter USB cordset employing #20 Gauge conductors (RFP RFI-50856)
The longest cable GlobTek recommends to be used with this product is USB cord GlobTek PNs USBA1M2MICROB20(R) and USBC1M0USBA(R), 1.2 Meters for best voltage regulation performance. (RFP RFI-20435-3)
4. Line Voltage Regulation: +/- 3% typical
5. Output Ripple (Vp-p): 150mV Ripples shall be measured with a 47uF electrolytic capacitor paralleled with a high-frequency 0.1uF ceramic capacitor across the output. The oscilloscope's bandwidth shall be set to 20MHz.
6. Turn-On/Turn-Off Overshoot: 5% maximum, 500 us maximum recovery time for 25% step load.
7. Turn-On Delay: 3000mS MAX at 115VAC Full Load
8. Hold-Up Time: 8mS Min at 100VAC Full Load
9. Inrush Current: No damage. On power when switching on/off repeatedly under any condition.
10. Switching Frequency: 66.5 KHz typical
11. Average Efficiency: 78.7% Min.(CEC&DOE Level VI Compliant), 79.0% Min. (ErP European Commission's Ecodesign Directive (2005/32/EC) / CoC Tier 2 Compliant)
12. Input Power(no load): < 0.1W < 0.1W, < 0.075W (ErP European Commission's Ecodesign Directive (2005/32/EC) / CoC Tier 2 Compliant)
1. Over-Voltage: Output shut down and auto restart
2. Over Temperature Protection: Output shut down and auto restart
3. Short Circuit Protection Output shut down and auto restart
4 Over Load Protection Output shut down and auto restart
5. Input Protection: Input line fusing
6. ESD: 8 kV Contact/20kV Air Discharge
1. Dielectric Withstand Voltage: 4000Vac or 5656Vdc 10mA 1 minute
2. Earth Leakage Current: N/A for Class II units, there is no PE Ground pin, so Earth Leakage current is not measured
3. Touch Current: Maximum allowed values: 100uA NC(Normal condition) 500uA SFC(single fault condition)
4. Means of Protection: 2 x MOPP
5. ROHS 2: Complies with EU 2011/65/EU and China SJ/T 11363-2006
1. Emissions, per EN 55032, EN 61000-6-3, EN 61000-6-4
Conducted Emissions: Class B, FCC Part 15, Class B
Radiated Emissions: Class B, FCC Part 15, Class B
2. Line Frequency Harmonics EN61000-3-2, Class A
3. Voltage Fluctuations/Flicker EN61000-3-3
4. Immunity, per EN 55024, EN 61000-6-1, EN 61000-6-2
Static Discharge Immunity EN61000-4-2, 8kV Contact Discharge, 15kV air discharge
Radiated RF Immunity EN61000-4-3, 3V/m 80-2700MHz, 80% 1KHz AM.
EFT/Burst Immunity EN61000-4-4, 2kV/100kHz.
Line Surge Immunity EN61000-4-5, 1kV differential, 2kV common-mode
Conducted RF Immunity EN61000-4-6, 3Vrms, 80% 1KHz AM
Power Frequency Magnetic Field Immunity EN61000-4-8, NA
Voltage Dip Immunity EN61000-4-11, Criteria
1. USB2.0 , BC1.2 compliant
2. MTBF: 200,000 hours @ 25°C ambient temperature
3. Operating Temperature: 0°C to 40°C ambient temperature
4. Humidity: 0% to 95% relative humidity
5. Storage Temperature: -40°C to 80°C
1. Housing: High impact plastic, 94V0 polycarbonate, non-vented
2. Markings: Label and/or Pad Printed and/or Molded in the case
|Individual Box/Gift Box Size (mm)||74 x 35 x 42|
|Individual Box/Gift Box Color||White|
|Master Carton Size (mm)||544 x 375 x 151|
|Gross Weight (kg)||14.8|
|Label Width (mm)||28.5|
|Label Height (mm)||17.5|
|Description||Blade Options for Q Series Wall Plug-in Power SuppliesData Sheet: http://en.globtek.com/interchangeable-blades.php|
Insertion Instructions: http://www.globtek.com/pdf/Instructions-Interchangeable-Blades.pdf
Video: Q-Blade Style Instruction Video
INPUT CONNECTOR: Q-Socket (below are available blades configurations which are "not included" (unless stated above); can be purchased separately, package with power supply or as a separate "Q-KIT" if specified
01. United States / Canada / Japan NEMA 1-15P/ IEC PLUG Type A [WORKS IN PLUG B] configuration: NA 2 blades, Class II; US/CA/JP P/N: Q-NA(R)
01. Q-KIT: 1,2,3,4 above
|Common output connector options:|
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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.
|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.
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).
What is European CoC Tier 2 Regulation?European CoC Tier 2 Regulation is a set of efficiency targets for external power supplies and AC adapters published by the The European Commission JRC (Joint Research Centre) Renewable Energy Unit. These targets are voluntary and not mandated by any law.
What is a Plug-in AC-DC Adapter?
Plug in AC-DC adapters are also known as AC Adaptors or AC-DC converters and are a type of external power supply. Some electrical appliances require power but lack the internal components to derive the required voltage and power from mains power. This is where an AC adapter is used to convert the AC current into DC voltage
How Does an AC-DC Wall Adapter Work?
The AC to DC adapter or external power supply consists of a power supply which is enclosed in a housing similar to an AC plug, hence the term plug type, wall plug in, plug-in or plugtop power adapter. The power supply is plugged into the mains socket and the AC Voltage is then converted by the AC to DC adapter power supply into a DC voltage that is fed into the appliance via the output cable connection.