GTM41133-90VV-x.x-F Open Frame/Internal Medical Power Supply Datasheet

GTM41133-90VV-x.x-F
GTM41133-90VV-x.x-F, Medical Power Supply,  60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-400Hz, Tyco 640445-5 3 Position Header PIN 1: EARTH, PIN 3: LINE, PIN 5: NEUTRAL, remove Pins 2 and 4, Output Rating: 90 Watts, Power rating with convection cooling (W) , 12-48V in 0.1V increments, Approvals: CB 60950; S-Mark 62368; IRAM; Morocco; UKCA; Conforms to 62368-1; CB 62368; Malaysia  12,15,18,19,24,26,28,36 & 48V only; Book 60601; CE; CE; cETLus ES60601; cETLus 60601-1 3rd; ETL; China RoHS; Class I; GOST-R; Level V; RoHS; Ukraine; WEEE; CB 60601-1 2MOPP; S-Mark 60950; RCM; CE; EAC; Serbia; S-Mark IEC/EN 60601-1; CB 60601-1; GTM41133-90VV-x.x-F, Medical Power Supply,  60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-400Hz, Tyco 640445-5 3 Position Header PIN 1: EARTH, PIN 3: LINE, PIN 5: NEUTRAL, remove Pins 2 and 4, Output Rating: 90 Watts, Power rating with convection cooling (W) , 12-48V in 0.1V increments, Approvals: CB 60950; S-Mark 62368; IRAM; Morocco; UKCA; Conforms to 62368-1; CB 62368; Malaysia  12,15,18,19,24,26,28,36 & 48V only; Book 60601; CE; CE; cETLus ES60601; cETLus 60601-1 3rd; ETL; China RoHS; Class I; GOST-R; Level V; RoHS; Ukraine; WEEE; CB 60601-1 2MOPP; S-Mark 60950; RCM; CE; EAC; Serbia; S-Mark IEC/EN 60601-1; CB 60601-1;GTM41133-90VV-x.x-F, Medical Power Supply, 60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-400Hz, Tyco 640445-5 3 Position Header PIN 1: EARTH, PIN 3: LINE, PIN 5: NEUTRAL, remove Pins 2 and 4, Output Rating: 90 Watts, Power rating with convection cooling (W) , 12-48V in 0.1V increments, Approvals: CB 60950; S-Mark 62368; IRAM; Morocco; UKCA; Conforms to 62368-1; CB 62368; Malaysia 12,15,18,19,24,26,28,36 & 48V only; Book 60601; CE; CE; cETLus ES60601; cETLus 60601-1 3rd; ETL; China RoHS; Class I; GOST-R; Level V; RoHS; Ukraine; WEEE; CB 60601-1 2MOPP; S-Mark 60950; RCM; CE; EAC; Serbia; S-Mark IEC/EN 60601-1; CB 60601-1; GTM41133-90VV-x.x-F, Medical Power Supply, 60601-1-4th Ed. , Open Frame/Internal, Regulated Switchmode AC-DC Power Supply AC Adaptor, , Input Rating: 100-240V~, 50-400Hz, Tyco 640445-5 3 Position Header PIN 1: EARTH, PIN 3: LINE, PIN 5: NEUTRAL, remove Pins 2 and 4, Output Rating: 90 Watts, Power rating with convection cooling (W) , 12-48V in 0.1V increments, Approvals: CB 60950; S-Mark 62368; IRAM; Morocco; UKCA; Conforms to 62368-1; CB 62368; Malaysia 12,15,18,19,24,26,28,36 & 48V only; Book 60601; CE; CE; cETLus ES60601; cETLus 60601-1 3rd; ETL; China RoHS; Class I; GOST-R; Level V; RoHS; Ukraine; WEEE; CB 60601-1 2MOPP; S-Mark 60950; RCM; CE; EAC; Serbia; S-Mark IEC/EN 60601-1; CB 60601-1;
Information
Model NumberGTM41133-90VV-x.x-F
Agency Documentshttp://globtek.info/certs/GTM41133/
CE EC-Declaration for Medicalhttps://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000JCFgXEAX
CE EC-Declaration for Industrial/Commercial/ITEhttps://globtek.secure.force.com/models/ec_declaration?id=a0Oa000000JCFgXEAX
CE EC-Declaration for HouseholdContact GlobTek for more information
UKCA-Declaration for Medicalhttps://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000JCFgXEAX
UKCA-Declaration for Industrial/Commercial/ITEhttps://globtek.secure.force.com/models/ukca_declaration?id=a0Oa000000JCFgXEAX
UKCA-Declaration for HouseholdContact GlobTek for more information
Morocco SDoC Declarationhttps://globtek.secure.force.com/models/Morocco_SDoC_Declaration?id=a0Oa000000JCFgXEAX
RoHS/RoHS3 Declarationhttps://www.globtek.com/pdf/rohs_cert/a0Oa000000JCFgXEAX
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~, 50-400Hz
Max Input Current (A)1.5A
Max Output Power Rating (W)90
Output Voltage Range (V)12-48
EfficiencyV
Ingress Protection
Size (mm)184*62*25
Enclosure
User-added image

 
Rating Table
Model Number (Final ordering #/Part No to be defined)Voltage (V)Current (A)Power (W)RFQ
GTM41133-9024-6.0-F*18590
GTM41133-9016-4.0-F*127.590
GTM41133-9016-1.0-F*151.0615.9
GTM41133-9024-5.0-F*194.7389.87
GTM41133-9024-F*243.7590
GTM41133-9048-10.5-F*37.52.490
GTM41133-9048-12.0-F*362.590
GTM41133-9048-F*481.87590
* (Final ordering #/Part No to be defined)
Specifications
A) ELECTRICAL SPECIFICATIONS:
01. Input Voltage: Specified 90-264 Vac, Nameplate rated: 100-240Vac
02. Input Frequency: Specified 47-63 Hz, Nameplate rated 50-60Hz
03. Output Regulation: +/- 5% measured at the output connector
04. Line Voltage Regulation: +/- 1% typical measured at full load
05. Output Ripple (Vp-p): +/-1% or 150 mV whichever is greater, 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
06. Turn-ON/OFF Overshoot: 5% maximum, 1 mS typical recovery time for 25% to 50% step load
07. Turn-ON Delay: 1 sec, maximum @ full load, nominal line
08. Hold-Up Time: 8 mS typical @ nominal input voltage and full load
09. Inrush Current: 30/60A maximum cold start @ 115/230Vac input
10. Switching Frequency: 65 KHz typical

B) PROTECTION
01. Over-Voltage: Electronically Protected Zener clamp across the output
02. Short Circuit: Electronically Protected unit will auto recover upon removal of fault
03. Input Protection: Input line fusing

C) SAFETY
01. Dielectric Withstand Voltage: 5656Vdc from primary to secondary
02. Earth Leakage Current: Did not exceed 5 mA in NORMAL CONDITION and 10 mA in SINGLE FAULT CONDITION
03. Earth continuity test:<0.1 Ohm or < 0.2 Ohm when with a non-detachable Power Supply cord, Class I Only
04 Touch Current: Did not exceed 100uA NC(Normal condition) 500uA SFC(single fault condition)
05. Primary to Secondary Isolation: 2 MOPP

D) OTHER:
01. MTBF: 200,000 Hours @ 25°C ambient temperature
02. Operating Temperature: 0°C to 40°C ambient temperature
03. Humidity: 0% to 90% relative humidity
04. Storage Temperature: -10°C to 80°C
05. Cooling: Convection
06. Operating Altitude: 5,000 METERS
07. Operating Atmospheric Pressure: 700 hPa TO 1060hPa

E) ENCLOSURE
01. Open Frame
02. Size: 156.0 x 55.2 x 24.1 +/-1.0 mm
03. LED to indicate "Power Out"
04. Markings: Label
Derating Curve
Qty (ea.)/Carton32
Individual Box/Gift Box Size (mm)Egg Crate
Individual Box/Gift Box Color
Master Carton Size (mm)470 x 370 x 210
Gross Weight (kg)15.6
Label Width (mm)30.0
Label Height (mm)23.0
Input Configuration
DescriptionTyco 640445-5 3 Position Header PIN 1: EARTH, PIN 3: LINE, PIN 5: NEUTRAL, remove Pins 2 and 4Product Details: http://www.te.com/catalog/pn/en/640445-5?RQPN=640445-5

User-added image
 
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)

No Logo Applicable

IEC 60950-1:2005 (Second Edition) + Am 1:2009 + Am 2:2013
User-added image
 
S-Mark Certificate EN 62368-1:2014 + A11 (http://www.intertek.com/marks/s/)
User-added image
PRECAUCION: PARA USO EN EQUIPOS ELECTRONICOS SOLAMENTE
 
IRAM certificate DC-E-G71-005.1 to IEC 62368-1:2014
User-added image
 
Morocco approval to IEC IEC 62368-1:2014
User-added image
 
UKCA Certification
Conforms to UL STD. 62368-1
Certified to CSA STD C22.2 NO.62368-1
Conforms to UL STD. 62368-1 Certified to CSA STD C22.2 NO.62368-1

No Logo Applicable

CB for IEC 62368-1:2014 (Second Edition)
No Logo Malaysia ST Release Letter GTM41133 IEC 62368-1:2014 (ED.2) No logo 12,15,18,19,24,26,28,36 & 48V only
User-added image60601-1 3rd Operating Instructions
User-added image  CE Mark: tested to comply with EN55022:2006/A1:2007 Class B, EN610003-2, EN610003-3 including EN61000-4-2, EN61000-4-3, EN61000-4-4, EN61000-4-5, EN61000-4-6N EN61000-4-11; EMI: Complies with EN55011 CLASS B and FCC Part 15B - On label or Molded in case
User-added image  CE Mark: tested to comply with EN 60601-1-2:2015 Medical electrical equipment Part 1-2: - Mark is on the label or Molded in the case
Conforms to ANSI/AAMI ES 60601-1:2005
Cert.to CAN/CSA Std. C22.2
 
cETLus ANSI_AAMI ES60601-1_2005
User-added image
 
cETLus-Cert-4007497 ANSI/AAMI ES60601-1:2005 with AMD C1: 2009, AMD C2: 2010 and CAN/CSA-C22.2 No. 60601-1 2008 with COR 2:2011+ANSI/AAMI HA60601-1-11 Ed:1
User-added imageInformation Technology Equipment Safety Part 1: General Requirements >Valid without technical revision: 01Jan2022< [UL 60950-1:2007 Ed.2 +R:14Oct2014]
User-added imageCHINA SJ/T 11364-2014, China RoHS Chart: http://en.globtek.com/globtek-rohs.php
User-added image
 
GOST-R mark for Russia(Document: http://www.globtek.com/html/iso_certificates/GT_GOST-R.pdf). 03/15/2015. Due to lack of demand, GlobTek will not be renewing it's GOST certification. Please contact your sales engineer for pricing on EAC.
User-added imageIndoor Use Only - Mark is on the label or Molded in the case
 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 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
No Logo ApplicableCB report IEC 60601-1: 2005 + CORR. 1 (2006) + CORR. 2 (2007) and or EN 60601-1:2006 3rd Edition 2xMOPP
User-added imageS-Mark Certificate EN 60950-1:2006 + A11:2009 + A1:2010 + A12:2011+A2:2013 (http://www.intertek.com/marks/s/)
User-added imageRCM certificate SAA-170038-EA; Australia and New Zealand Regulatory Compliance, Mark (http://rcm.standards.org.au/rcmfaq/rcmfaq.htm)
User-added image  CE Certification CE Mark: tested to comply with EN 55032.2012+AC.2013 EN 61000-3-2.2014 EN 61000-3-3.2013 EN 60601-1-2.2015 EN 55024.2010
User-added image  Certification # TC RU AR46.B.59626 Custom Union of Russia, Belarus and Kazakhstan
User-added imageSerbia Approval - Conformity mark must be at least 5 mm high.
User-added imageSemko S-Mark-Cert-EN60601-1 3.1rd Edition (http://www.intertek.com/marks/s/)
No Logo IEC 60601-1: 2005 +A1 and IEC 60601-1-11:2015
Popular Products (Stock items)
SKUVolts OutCurrent Out (Amps)ConnectorRFQSample Request
18044036.02.5
17501424.03.75
32423712.07.5
17624612.07.5
21703124.03.8
20056116.05.6
17729718.05.0
18995415.06.0
18041430.03.0
360256
19888524.73.6
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 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 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.

Request Info
Call
Email
💬
Text
💁
Chat
?
Request a Quote
Can we help you?
Can we help you?