Global Medical Technology

Strategic Investment For The Best Solutions

GMT | Global Medical Technology

Global Medical Technology, SL (GMT) began operations in 1998 in the field of aesthetics, specializing in the development, marketing and maintenance of equipment intended for hair removal, weight loss and skin treatments using non-invasive methods.

GMT, with its headquarters in Madrid (Spain) and present in various countries, manufactures and distributes leading aesthetics devices, according to each country’s standards, representing a quality benchmark at a competitive cost distinguished by a unique developed systems.

The constant investment in Research and Development has allowed the Platinum GMT™ Series to be one of the worldwide most well-known and technologically advanced devices. Over 1,500 cosmetic clinics in different countries use GMT devices.

GMT has developed the Platinum GMTTM series, composed of high-quality, easy-to-use equipment at very competitive prices, which covers a broad range of cosmetic treatments. Thanks to its investment in R&D, GMT continues to broaden the amount of products that it has to offer, increasing the applicable treatments and integrating several into multi-function devices.

Competitive GMT Advantages

What really sets GMT apart

  • Proven Results. Years on the market and the number of clinics using our technology are the main guarantee of quality.
  • Exclusive GMT Cloud technology allows owners full remote control of their operation clinics (sessions, schedules, operators…), accessing the system in real time from anywhere via Internet-connected devices. It allows GMT customer service to monitor the equipment to prevent breakdowns and to repair them online when needed, reducing downtime of the device.
  • The GMT Department of Education trains and certifies all personnel in charge of providing aesthetic services and answering questions regarding treatments, ensuring this way that no competitor will have the same level of service, knowledge or attention to their customers.
  • Treatment Speed. Of all similar devices currently in the market, these have the highest performance pulses per minute and footprint size, ensuring an efficient service.
  • High performance. Its unique cooling system with sapphire crystals allows these systems to be working for hours without overheating.
  • Easy to use. Its proprietary and intuitive software automatically calculates all parameters in just three steps
  • Computer Monitoring.To keep both users and clients records.
  • System Upgrades. Allows clinics using these devices to ensure appropriate technological responses to market’ improvements.

Technical Services

Global Medical Technology has its own technical service so that in case of breakdown the customer response is immediate and in most cases the problem fixed in less than 24 hours after contacting customer service..

Our Certifications

Our devices are endorsed by competent authorities

  • UNE – EN 60335 – 2 – 27:2005
  • UNE – EN 60355 – 1:2002 + A11:2004 + A1:2005 + ERR:2005 + A12:2006 + CORR:2007 + A2:2007 + A13:2009
  • UNE – EN 55014 – 1:2008
  • UNE – EN 61000 – 3 – 2:06
  • UNE – EN 61000 – 3 – 3:97 + A1:02 + C:99 + A2:06
  • UNE – EN 55014 – 2:98 + A1:02
  • UNE – EN 61000 – 4 – 2:97 + A1:99 + A2:01
  • UNE – EN 61000 – 4 – 3:07
  • UNE – EN 61000 – 4 – 4:05
  • UNE – EN 61000 – 4 – 5:07
  • UNE – EN 61000 – 4 – 6:08
  • UNE – EN 61000 – 4 – 11:06
  • FDA (U.S. Food and Drug Administration) Ref.: K140668

EN 60601 – 1 – 2 (2007):

EM Emission

  • EN 55011 (2007) / A2 (2007): Radiated (Group 1 Class B)
  • EN 55011 (2007) / A2 (2007): Conducted (Class B)
  • EN 55014 – 1 (2006) / A1 (2009): Discontinuous Conducted
  • EN 61000 – 3 – 2 (2006) / A1 (2009) / A2 (2009): Fluctuating harmonics
  • EN 61000 – 3 – 3 (2008): Fluctuations and flickers

EM Immunity

EN 61000 – 4 – 3 (2006): EM radiated field of RF
EN 61000 – 4 – 4 (2004): EFT burst
EN 61000 – 4 – 5 (2006): Surges
EN 61000 – 4 – 6 (2007): RF common mode
EN 61000 – 4 – 8 (1996) / A1(2001): 50Hz H field
EN 61000 – 4 – 11 (2004): Dips. interruptions
EN 61000 – 4 – 2 (1995) / A1 (1998) / A2 (2001): ESD

Certificate No. 2107 / 2407 / 1325 – CER, carried out at a laboratory accredited by ENAC, with a Certificate of Accreditation No.5 / LE260, in accordance with Test Reports No. 2107 / 1325 y N° 2407 / 1325

Certificate No. 31857 CEM.001, carried out at a laboratory accredited by ENAC, with a Certificate of Accreditation No.51 / LE203

IEC SYSTEM for Conformity Testing and Certification of Electrical Equipement (IECEE), Geneva, Swizertland

Safety of household and similar electrical appliances.
Particular requirements for appliances for skin exposure to ultraviolet and infrared radiation.

Test Report Form N° IECEN60335_2_27A

Test Specification:
IEC 60335-2-27:2002 Fourth Edition Used in Conjuction with IEC 60335-1:2001 (Fourth Edition) + Corrigendum1:2002 + A1:2004 + A2:2006
IEC 60335-2-27:2002 Fourth Edition Used in Conjuction with IEC 60335-1:2001 (Fourth Edition) + Corrigendum1:2002 + A1:2004 + A2:2006
EN 60335-2-27:2003 used in conjunction with EN 60335-1:2002 + A1:2004 + A11:2004 + A2:2006 + A13 + 2008

Approved by the IQC Certification Approval Committee, at its session on 27/05/2010 (Record N° 13928)

TYPE-T 2810 / 1 APPROVAL CERTIFICATE in accordance with test report No.: 9270-642 – 001 – 10096

Tests for the evaluation of the design and verification of compliance with basic electromagnetic safety standards. Disposition 736 / 99 D.N.C.I., Art. 1 – Inc. b at a laboratory recognized with no. 1045 / 1999 + 582 / 2001

Complying with regulations:
IEC 60335-1 (Ed. 4.2):2006 +
IEC 60335-2-27(Ed. 4):2002 + A1:04 + A2:07

CE Compliance Declaration:
Directive Low voltage 2006 / 95 / EC
Directive electromagnetic compatibility 2004 / 108 / EC

Supervised by the Spanish Medications and Health Products Agency. MINISTRY OF HEALTH as an aesthetic device. Registration No.: 23142 / RG44869

Verified by the Universidad Complutense de Madrid Center of Research Assistance, in accordance with the X-Ray Fluorescence Covering Chemical Composition Analysis report.

Health Registry INVIMA 2011-DM – 0007511 National Institute of Medication and Food Vigilance, in accordance with resolution No. 2011023065

IEC 60335-1: 2010 / IEC 60335-2-23:2003 + A1:2008
EN 60335-1: 2012 / EN 60335-2-23:2003 + Corr:2009 + A1:2008 +A11:2010
UNE-EN 60335-1: 2012 / UNE-EN 60335-2-23: 2004 + Corr:2009 + A11:2004 + A1:2009 + A11:201
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