GTM91120-30VV-DW
GTM91120-30VV-DW, Medical Power Supply,  60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Solder Pins for Line & Neutral, 1.4 mm square pins, 4.5 mm long, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: China RoHS; Level V; RoHS; Ukraine; VCCI; WEEE; PSE; CB 60335; GTM91120-30VV-DW, Medical Power Supply,  60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Solder Pins for Line & Neutral, 1.4 mm square pins, 4.5 mm long, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: China RoHS; Level V; RoHS; Ukraine; VCCI; WEEE; PSE; CB 60335;GTM91120-30VV-DW, Medical Power Supply, 60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Solder Pins for Line & Neutral, 1.4 mm square pins, 4.5 mm long, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: China RoHS; Level V; RoHS; Ukraine; VCCI; WEEE; PSE; CB 60335; GTM91120-30VV-DW, Medical Power Supply, 60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-60 Hz, Solder Pins for Line & Neutral, 1.4 mm square pins, 4.5 mm long, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: China RoHS; Level V; RoHS; Ukraine; VCCI; WEEE; PSE; CB 60335;
Information
Model NumberGTM91120-30VV-DW
Agency Documentshttp://www.globtek.info/certs/GTM91120-T2%20-T3A%20-FW/
CE EC-Declaration for Medicalhttps://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000FkeUoEAJ
CE EC-Declaration for Industrial/Commercial/ITEhttps://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000FkeUoEAJ
CE EC-Declaration for HouseholdContact GlobTek for more information
UKCA-Declaration for Medicalhttps://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000FkeUoEAJ
UKCA-Declaration for Industrial/Commercial/ITEhttps://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000FkeUoEAJ
UKCA-Declaration for HouseholdContact GlobTek for more information
Morocco SDoC Declarationhttps://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0Oa000000FkeUoEAJ
RoHS/RoHS3 Declarationhttps://www.globtek.com/pdf/rohs_cert/a0Oa000000FkeUoEAJ
Prop 65 Statementhttps://en.globtek.com/prop-65-statement.pdf
REACH Declarationhttps://www.globtek.com/pdf/iso_certificates/REACH.pdf
Conflict Minerals Declarationhttps://www.globtek.com/pdf/conflict-minerals.pdf
Model Parameters
TypeOpen Frame/Internal
TechnologyRegulated Switchmode AC-DC Power Supply AC Adaptor
CategoryMedical Power Supply
Input Voltage Range (V)100-240V~, 50-60 Hz
Max Input Current (A)1.5A
Max Output Power Rating (W)30
Output Voltage Range (V)5-48
EfficiencyV
Ingress Protection
Size (mm)
Enclosure
Rating Table
Model Number (Final ordering #/Part No to be defined)VoltageAmps (A)Watts (W)RFQ
* (Final ordering #/Part No to be defined)
Specifications
  1. ELECTRICAL SPECIFICATIONS:
    1. Input Voltage: 100-240 Vac
    2. Input Current: 1.5 A RMS max
    3. Input Frequency: 47 - 63 Hz
    4. Output power (rated): 30Watts max
    Note: Refer to Power Supply information on page 2 for the corresponding rated output power for the specific output voltage.
    5. Output Regulation: +/- 5% measured at the output connector
    6. Line Voltage Regulation: +/- 2% typical measured at full load
    7. Output Ripple (Vp-p): +/-2% maximum, measured at 20 MHz bandwidth with 0.1 uf ceramic capacitor in parallel with 10 uf electrolytic capacitor connected at the end of the output connector at nominal line
    Optional low ripple option available (RFP4579)
    8. Turn-ON/OFF Overshoot: 5% maximum, 500uS typical recovery time for 25% to 50% step load
    9. Turn-ON Delay: 3 Seconds, maximum @ full load, nominal line
    10. Hold-Up Time: 8mS typical @ nominal input voltage and full load
    11. Inrush Current: 60A maximum cold start @ 240Vac input
    12. Switching Frequency: 100 KHz typical

    B) PROTECTION
    1. Over-Voltage: Protected with a Zener diode clamp across the output
    2. Short Circuit: Hiccup with auto recovery
    3. Over-load: Hiccup with auto recovery
    4. Input Protection: Input line and neutral fusing

    C) SAFETY

    1. Dielectric Withstand Voltage: 5656Vdc from primary to secondary
    2. Warning to service personnel "CAUTION: Double pole/neutral fusing".  This marking is required only for both F1 and F2 installed
    3. Earth Leakage Current: <100 uA at 240Vac input voltage
    4. MTBF: 200,000 hours @ 25°C ambient temperature
    5. Operating Temperature: 0°C to 40°C ambient temperature

    D) OTHER:
    1. MTBF: 200,000 Hours @ 25°C ambient temperature
    2. Humidity: 0% to 90% relative humidity
    3. Storage Temperature: -10°C to 80°C
    4. Cooling: Convection
Derating Curve
Qty (ea.)/Carton
Individual Box/Gift Box Size (mm)
Individual Box/Gift Box Color
Master Carton Size (mm)TBD
Gross Weight (kg)
Label Width (mm)TBD
Label Height (mm)TBD
Input Configuration
DescriptionSolder Pins for Line & Neutral, 1.4 mm square pins, 4.5 mm long
Approvals

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.

LogoDescription
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: http://en.globtek.com/globtek-rohs.php
 User-added image

Efficiency: complies to section 301 of Energy Independence and Security Act (EISA) complies with Energy Star tier 2 (North America), ECP tier 2 (China), MEPS tier 2 (Australia), Code of Conduct (Europe)
RoHSSpecifications of directive 2011/65/EU Annex VI (ROHS-2) with amendment 2015/863-EU (ROHS-3) http://www.ce-mark.com/Rohs%20final.pdf
User-added imageUkraine UKRSepro (Document: www.globtek.com/html/iso_certificates/GT_Ukraine.pdf)
User-added imageJapan: Voluntary Control Council for Interference (VCCI)
 User-added imageWEEE: Complies with EU 2012/19/EU (http://ec.europa.eu/environment/waste/weee/index_en.htm) Mark is on the label or Molded in the case
User-added imageJAPAN TUV Rheinland-PSE GlobTek Inc to J60950-1(H26) , J55022(H22),J3000(H25).Please follow the procedure listed in the following link for proper import to Japan: http://en.globtek.com/importing-to-japan.php.

No Logo Applicable

IEC 60335-1:2010 (Fifth Edition) incl. Corr. 1:2010 and Corr. 2:2011 + A1:2013
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38099712.02.5
What is a IEC 60601-1-11 home healthcare power supply?

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 an open frame or internal AC-DC Power supply?

Open frame AC-DC power supplies are also known as AC-DC converters and are a type of internal power supply. The open frame AC to DC power supply is built into the inside of a system and used to convert the AC current into DC voltage.

What is IEC 60335-1?

The International Standard 60335-1 covers the safety of electrical appliances for household and similar purposes with rated voltage not more than 250 V for single-phase appliances and 480 V for other appliances.

Why is an IEC 60335-1 rated power supply or AC adapter necessary?

Applications used in the household environment are mandated to use and IEC 60335-1 certified power supply or AC to DC converter. These unique power supplies provide for specific compliance necessary for household use appliances.

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).

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.

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