Communication formats supported: USB Power Delivery (PD) 2.0/3.0, Quick Charge™ 2.0/3.0, Quick Charge™ 4.0/4.0+ with up to 7 voltages and VDM options available. Fully globally certified for Medical 60601-1, ICT 62368 Communication formats supported: USB Power Delivery (PD) 2.0/3.0, Quick Charge™ 2.0/3.0, Quick Charge™ 4.0/4.0+ with up to 7 voltages and VDM options available. Fully globally certified for Medical 60601-1, ICT 62368
300µA max. NC/SFC (N/A for 2-conductor input models)
Means of Protection:
2 x MOPP
Output Isolation Options:
-T2/R2 suffix: Class II 2-conductor (C8/C18 inlet or interchangeable blades) -T3/R3 suffix: Class II, with functional earth (FE) (C6/C14 inlet or interchangeable blades) Class I, earth wire connected directly to output negative (C6/C14 inlet or interchangeable blades)
High impact plastic, 94V0 polycarbonate, non-vented Desktop T2/T3: C6, C8, C14, or C18 IEC inlet Hybrid (desktop or wall plug-in): Class I or Class II input
No suffix: Captive 1.5m shielded USB Type-C cable -RA suffix: Female USB Type-C connector integrated into housing
Adhesive backed label or laser engraving
Prevention of Unauthorized Use
USB Power Delivery:
In critical applications, the use of a non-authorized USB PD power adapter may pose a substantial risk to system safety or performance.
The power adapter's identity may be checked and validated prior to PD contract negotiation by use of USB PD Vendor Defined Messages (VDMs). The power adapter will respond to a USB PD “Discover Identity” VDM with 0x4754 in the “ProductID” field.
Additionally, non-standard 5.8V and 15.1V PDOs are included. Host systems may be designed to reject a power adapter which does not contain one of these PDOs.
These measures do not guarantee a secure implementation, and are only suggested as a method of risk mitigation.
This series of Interchangeable Blade products may be used with Proprietary Interchangeable Blades as described below or with standard international power cords.
Optional INPUT BLADES: R-Socket: below are available blades configurations which are "not included" (unless stated above); may be purchased separately, packaged with power supply, or as a separate "R-KIT" if specified
Standard Cordsets Below are standard cordsets which are "not included" (unless stated above); these may be purchased separately or packaged with the power supply. Contact your Sales Engineer if the style required is not shown below. Many more available in different lengths, colors or cable material.
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.
Medical 4th Ed.
EN/IEC 60601-1-2, 4th Edition (Please visit EMC reports for further info)
Declaration ДС № ЕАЭС N RU Д-US.КА01.В.10453_19 Custom Union of Russia, Belarus and Kazakhstan http://www.globtek.com/redirect/?loc=gost-certificate-eac-declaration
CHINA SJ/T 11364-2014, China RoHS Chart: http://www.globtek.com/pdf/F-GT-DJD-8.4.1-006%20China%20RoHS%20Declaration%205-20-22.pdf
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)
JAPAN TUV R-PSE, Cert. No. JD50473430 , to J62368-1(H30) , J55032(H29),J3000(H25)[DC15? 30V]. Please reference the following website for guidelines on PSE regulations: http://en.globtek.com/importing-ite-and-medical-power-supplies-ac-adaptors-to-japan/
Specifications of directive 2011/65/EU Annex VI (ROHS-2) with amendment 2015/863-EU (ROHS-3) http://www.ce-mark.com/Rohs%20final.pdf
Japan: Voluntary Control Council for Interference (VCCI)
WEEE: 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
CB report IEC60601-1 2005 A1+C1+C2 2016-2-4 and or EN 60601-1:2006 3.1rd Edition 2xMOPP (6W max)
CB Report IEC 60950-1:2005 (Second Edition) + Am 1:2009 + Am 2:2013 (GTM96605-G2-XX)
No Logo Applicable
CB for IEC 62368-1:2014 (Second Edition)
AAMI ES60601-1 Issued: 2012/08/20 Medical Electrical Equipment - Part 1: CAN/CSA-C22.2 No.60601-1:14, Third Edition Issued: 2014/03/01 - Medical Electrical Equipment - Part 1: IEC 60601-1-11 Issued: 2015/01/20 Ed. 2 Medical Elec. Equip.- Part 1-11:
Information Technology Equipment Safety Part 1: General Requirements (UL 60950-1 Issued: 2007/03/27, Ed: 2 Rev: 2014/10/14) Information Technology Equipment Safety Part 1: General Requirements (CSA C22.2 No. 60950-1 Issued: 2007/03/27 Ed: 2 (R2012) Amd.
Audio/Video, Information And Communication Technology Equipment - Part 1: Safety Requirements [UL 62368-1:2014 Ed.2]Audio/Video, Information And Communication Technology Equipment - Part 1: Safety Requirements [CSA C22.2#62368-1:2014 Ed.2]
Conforms to AAMI STD. ES60601-1 Certified to CAN/CSA STD.C22.2 NO.60601-1
Conforms to AAMI STD. ES60601-1,IEC 60601-1-11 Certified to CAN/CSA STD.C22.2 NO.60601-1
Indoor Use Only - Mark is on the label or Molded in the case