Preferred ratings shown below. Custom output voltages available in 0.1V increment from the minimum voltage listed to the maximum voltage listed; contact sales.
Model Number (Final ordering #/Part No to be defined)
Voltage (V)
Current (A)
Power (W)
RFQ
GTM9X1001P-10015-T2A*
15
6.666
99.99
GTM9X1001P-6015-T2A*
15
4
60
GTM9X1001P-10012-T2A*
12
8.33
99.96
GTM9X1001P-10018-T2A*
18
5.55
99.9
GTM9X1001P-10019-T2A*
19
5.26
99.94
GTM9X1001P-10024-T2A*
24
4.16
99.84
GTM9X1001P-10030-T2A*
30
3.33
99.9
GTM9X1001P-10036-T2A*
36
2.77
99.72
GTM9X1001P-10048-T2A*
48
2.08
99.84
GTM9X1001P-10054-T2A*
54
1.85
99.9
GTM9X1001P-WWWVV-T2A-XXXX
CUSTOM
CUSTOM
CUSTOM
* (Final ordering #/Part No to be defined)
Specifications
Features
Aerospace qualified (per RTCA/DO-160G)
IEC60601-1-11 "Home Healthcare" certified @ 80VAC
Extremely low input current distortion
Enhanced immunity capability
Exceptionally low inrush current
Low leakage current @ 400Hz input
Shock & vibration in accordance with IEC60601-1-12 (EMS) & DO-160G
-10°C to 40°C (100W) Check derating curve for T > 40°C.
Storage Temperature:
-40°C to 80°C
Humidity:
0% to 95% relative humidity, non-condensing
Altitude
5000m
Cooling:
Natural convection
Shock:
End use handling: Half-sine, <3ms duration, 1.65m/s, 3 shocks per face Transportation simulation: Trapezoid, 60G acceleration, 5.75m/sec, 3 shocks per face General shock: Half-sine, 100G acceleration, 6ms duration, 3 shocks per face
Vibration:
IEC60601-1-12, Section 10.1.3, Clause B DO-160G, Section 8, Procedure 8.8, Category U, Zone 1A
Bump:
EN1789, Clause 6.4.1
Drop:
EN1789, Clause 6.4.2
Ingress Protection:
IP43
RoHS:
Complies with EU 2015/863 and China SJ/T 11363-2006
Safety
Compliant Standards:
General medical: IEC60601-1 Home healthcare: IEC60601-1-11 (2-conductor input models only) Emergency medical services (EMS): IEC60601-1-12 (2-conductor input models only) Information & communications technologies (ICT): IEC62368-1
Dielectric Withstand Voltage:
4000VAC or 5656VDC from input to output 10mA, 1 minute
Below are standard cordsets which are "not included" (unless stated above); these may be purchased separately or packaged with the power supply. Please 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.
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.
Logo
Description
Medical 4th Ed.
EN/IEC 60601-1-2, 4th Edition (Please visit EMC reports for further info)
Japan: Voluntary Control Council for Interference (VCCI)
Indoor Use Only - Mark is on the label or Molded in the case
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
JAPAN TUV R-PSE, Cert. No. JD 50469658, to J62368-1(H30) , J55032(H29),J3000(H25)[DC30?60V]. Please reference the following website for guidelines on PSE regulations: http://en.globtek.com/importing-ite-and-medical-power-supplies-ac-adaptors-to-japan/
JAPAN TUV R-PSE, Cert. No. JD 50469658, to J62368-1(H30) , J55032(H29),J3000(H25)[15V or less]. Please reference the following website for guidelines on PSE regulations: http://en.globtek.com/importing-ite-and-medical-power-supplies-ac-adaptors-to-japan/
JAPAN TUV R-PSE, Cert. No. JD 50469658, 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/
RoHS
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
No Logo Applicable
CB for IEC 60601-1:2005 (Third Edition) + CORR. 1 (2006) + CORR. 2 pending (2007) + AM1 (2012) or IEC 60601-1 (2012 reprint) (Ed 3.1) up to 48V only
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
Medical Elec. Equip.- Part 1-11: Gen. Req. For Basic Safety & Essential Perf.- Collateral Standard - Req. For Medical Elec. Equip. & Medical Elec. Systems Used In The Home Healthcare Environment [IEC 60601- 1-11:2015 Ed.2] (pending)
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
UKCA Certification
CE Certification Class II CE Mark: tested to comply with EN 55032.2015+A1.2020 EN 61000-3-2.2019+A1:2021 EN 61000-3-3.2013 +A1:2019 + A2:2021 EN 55025 (pending)
No Logo Applicable
CB report IEC60601-1 2005 A1+C1+C2 2016-2-4 and or EN 60601-1:2006 3.1rd Edition 2xMOPP (pending)