|GTM96600-60VV-P2(SR with EU Plug 2 pin)|
|GTM96600-60VV-P2(SR with EU Plug 2 pin), ICT / ITE / Medical Power Supply/Class 2/Household Power Supply, 60601-1-4th Ed. , Potted/Encapsulated in plastic housing, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Europe Blades Class II, (2) Conductors, Output Rating: 60 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: CE; 230V CoC Tier 2; Ukraine; IP68; WEEE; China RoHS; Level VI; LPS 60950; EAC; RoHS; Double Insulation; S-Mark IEC/EN 60601-1; CB 60601-1; CB 60950; CB 62368; UKCA; cETLus 60601; cETLus 60950-1; CB 61158;|
|Model Number||GTM96600-60VV-P2(SR with EU Plug 2 pin)|
|CE EC-Declaration for Medical||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000Q0BaqEAF|
|CE EC-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000Q0BaqEAF|
|CE EC-Declaration for Household||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000Q0BaqEAF|
|UKCA-Declaration for Medical||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000Q0BaqEAF|
|UKCA-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000Q0BaqEAF|
|UKCA-Declaration for Household||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000Q0BaqEAF|
|Morocco SDoC Declaration||https://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0O0c00000Q0BaqEAF|
|Prop 65 Statement||https://en.globtek.com/prop-65-statement.pdf|
|Conflict Minerals Declaration||https://www.globtek.com/pdf/conflict-minerals.pdf|
|Type||Potted/Encapsulated in plastic housing|
|Technology||Regulated Switchmode AC-DC Power Supply AC Adaptor|
|Category||ICT / ITE / Medical Power Supply/Class 2/Household Power Supply|
|Input Voltage Range (V)||100-240V~, 50-60 Hz|
|Max Input Current (A)||1.5A|
|Max Output Power Rating (W)||60|
|Output Voltage Range (V)||5-48|
|Efficiency||USA DOE Level VI / Eco-design Directive 2009/125/EC, (EU) 2019/1782|
|3D File Download||https://www.globtek.com/file/dl/GTM96600-60VV-P2_SR_with_EU_Plug_2_pin.zip|
* (Final ordering #/Part No to be defined)
|Individual Box/Gift Box Size (mm)||158*78*65|
|Individual Box/Gift Box Color||White|
|Master Carton Size (mm)||490 x 410 x 300|
|Gross Weight (kg)||15.2|
|Label Width (mm)||79.5|
|Label Height (mm)||39.5|
|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.
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The FDA defines a home use medical device as “a device intended for users in a non-clinical or transitory environment, which is managed partly or wholly by the user, requires adequate labeling for the user, and may require training for the user by a healthcare professional in order to be used safely and effectively. This includes permanently and temporarily implanted devices and any type of equipment that a person may use to recover and rehabilitate.”
IEC 60601-1-11 is the current version of collateral standard IEC 60601-1 that applies to the basic safety and essential performance of medical electrical equipment used in home settings. Effective June 30, 2013 in the European Union and December 31, 2013 in the U.S., the new standard differs from the previous edition(s) in several key ways. It now requires a ‘Class II’ electrical categorization of medical equipment, an elevated ingress protection (IP), and systems for home use and expands the definition of the ‘home environment’ to include European nursing homes.
a IEC 60601-1-11 home healthcare power supply is an AC to DC converter which complies with the standards specified in IEC 60601-1-11. aside from the basic requirements for medical power supplies such as elevated dielectric with stand voltage and low leakage current home health care power packs also require to be Class II and a minimum ingress protection level of IP21. IEC 60601-1-11 is also listed inside of the product CB, UL, and other regulatory reports.
How do I know if I need an IEC 60601-1-11 home healthcare power supply adapter?
The final use application and where that device would be used would dictate if it's necessary to comply with IEC 60601-1-11 .
Are there any restrictions as to the type of power supply that could qualify as IEC 60601-1-11 ?
Most types of GlobTek medical power supplies and AC to dc adapters qualify as IEC 60601-1-11. GlobTek offers both external desktop or wall plug-in power supplies that meet the standard. The main constraints for the AC to DC adapters to meet IEC 60601-1-11 are that they are class II and have an elevated ingress protection level. 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.
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 an LPS (Limited power source)?
A Limited Power Source (LPS) as defined in IEC 62368-1 and IEC 60950, is a secondary circuit with an open circuit output voltage, UOC, not exceeding the SELV circuit limits of 42.4 VPEAK or 60 VDC. The maximum apparent power, S, available on the output under any load condition, and the maximum fault current, ISC, available on the output under any load condition, (including a short-circuit), are limited to magnitudes not likely to cause ignition under fault condition in components mounted on, or circuits constructed from, suitably rated materials.
Why is a LPS (limited power source) necessary?
Providing LPS (limited power source) limitations to part or all of the circuits in a product design gives the mechanical design more flexibility in polymeric material choices and openings in the enclosure, as a fire enclosure need not be provided for LPS-powered circuits.
Can a Class 2 power unit or UL1310 power supply be replaced by an LPS (limited power source)?
Many and product standards will stipulate the use of either an LPS rated 62368-1 power supply or AC to DC converter or a Class 2 power unit certified to UL 1310. If the end product standard allows for the substitution of a class 2 power unit with an LPS rated supply one may be used.
What is the difference between a Class 2 power unit certified to UL 1310 and a LPS (limited power source)?
UL1310 is a product safety standards which aims to keep humans safe by lowering the possibility of a hazardous situation. UL1310 requires that all AC/DC power supplies and AC/DC adapters carrying UL1310 certification have limited output power capability. The limits are defined in Section 28 of the standard. UL 1310 AC adapters and power supplies are also known as Class 2 Transformers. IEC62368-1 gives the name “Limited Power Source” (LPS) to a class of AC to DC and DC to DC power supplies which meet a set of criteria defined in Annex Q of the standard. It is important to note that a power supply certified to IEC62368-1 does not imply that it also LPS compliant; LPS compliance is optional. The two essentially require the same technical requirements but differ in marking requirements on the nameplate.
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.