|GTM91120-30VV-P2(SR with SAA Plug 2 pin)|
|GTM91120-30VV-P2(SR with SAA Plug 2 pin), ICT / ITE / Medical 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, Australian AS 3112 configuration: SAA 2 pins Class II, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: EAC; Fuse 60335; Book 60601; CB 60601-1; CB 60335; CB 60950; CB EN/IEC 60335-1; CE; CE; ETL; China RoHS; cRUus (up to 30V); cRUus; Double Insulation; FCC; IEC 60335; IEC/EN60601-1; IEC/EN60950-1; IP68; Level V; LPS 60950; SIQ; SIQ; Ukraine; VCCI; WEEE; GTM91120-30VV-P2(SR with SAA Plug 2 pin), ICT / ITE / Medical 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, Australian AS 3112 configuration: SAA 2 pins Class II, Output Rating: 30 Watts, Power rating with convection cooling (W) , 5-48V in 0.1V increments, Approvals: EAC; Fuse 60335; Book 60601; CB 60601-1; CB 60335; CB 60950; CB EN/IEC 60335-1; CE; CE; ETL; China RoHS; cRUus (up to 30V); cRUus; Double Insulation; FCC; IEC 60335; IEC/EN60601-1; IEC/EN60950-1; IP68; Level V; LPS 60950; SIQ; SIQ; Ukraine; VCCI; WEEE;|
|Model Number||GTM91120-30VV-P2(SR with SAA Plug 2 pin)|
|CE EC-Declaration for Medical||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000PzSZhEAN|
|CE EC-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ec_declaration?id=a0O0c00000PzSZhEAN|
|CE EC-Declaration for Household||Contact GlobTek for more information|
|UKCA-Declaration for Medical||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000PzSZhEAN|
|UKCA-Declaration for Industrial/Commercial/ITE||https://globtek.secure.force.com/models/ukca_declaration?id=a0O0c00000PzSZhEAN|
|UKCA-Declaration for Household||Contact GlobTek for more information|
|Morocco SDoC Declaration||https://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0O0c00000PzSZhEAN|
|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|
|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|
MYLAR CASE COVER INSTALLED
* (Final ordering #/Part No to be defined)
|A) ELECTRICAL SPECIFICATIONS:|
1. Input Voltage: Specified 90-264 Vac, Nameplate rated: 100-240Vac
2. IInput Frequency: Specified 47-63 Hz, Nameplate rated 50-60Hz
3. Output Regulation: 8%- 5% measured at the output connector
4. Line Voltage Regulation: +/- 2% typical measured at full load
5. 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)
6. Turn-ON/OFF Overshoot: 5% maximum, 500uS typical recovery time for 25% to 50% step load
7. Turn-ON Delay: 3 Seconds, maximum @ full load, nominal line
08. Hold-Up Time: 5mS typical @ nominal input voltage and full load
09. Inrush Current: 60A maximum cold start @ 240Vac input
10. Switching Frequency: 100 KHz typical
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
1. Dielectric Withstand Voltage: 5656Vdc from primary to secondary
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)
1. MTBF: 200,000 Hours @ 25°C ambient temperature
2. Operating Temperature: -10°C to 40°C ambient temperature (RFP RFI-50576)
3. Humidity: 0% to 90% relative humidity
4. Storage Temperature: -10°C to 80°C
5. Cooling: Convection
6. ROHS 2: Complies with EU 2011/65/EU and China SJ/T 11363-2006
7. For EMI suppression 28A026-0A2 Snap-on Ferrites are recommended on both input and output cables, if required.
1. Housing: High impact plastic, 94V0 polycarbonate, non-vented
2. Size: 97.23 x 46.23 x 32.0 +/- 1.0 mm
3. Markings: Label and/or Pad Printed and/or Molded in the case
4. Ingress Protection: IP68, Dust Tight, No ingress of dust, complete protection against contact as well as Protected against liquid Immersion beyond 1 m
|Individual Box/Gift Box Size (mm)||142 x 62 x 60|
|Individual Box/Gift Box Color||White|
|Master Carton Size (mm)||442 x 330 x 275|
|Gross Weight (kg)|
|Label Width (mm)||59.5|
|Label Height (mm)||29.5|
|Description||Australian AS 3112 configuration: SAA 2 pins Class II|
Used in Australia, New Zealand, Fiji, Papua New Guinea and Tokelau, has two flat pins forming an inverted V-shape. These flat blades measure 6.3 by 1.5 mm with the Active and Neutral pins of 17 mm in length set 30° to the vertical on a nominal pitch of 13.7 mm. A standard power outlet in Australia provides a nominal voltage of 230 volts at a maximum of 10 amps and always includes an earth connection. As in the UK, its outlets are individually switched for extra safety. Argentina uses a similar plug, with pins 1 mm longer.
|Common output connector options:|
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|Popular Products (Stock items)|
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 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.