Prices available to wholesalers only.


The RMD is a unique rejuvenation system which aims to satisfy the need to improve one’s wellbeing by significantly reducing the signs of aging through non-invasive, non-surgical means. Our device is designed to distinctively support the treatment of skin texture, the smoothing of age-related expression lines, the tightening of pores and the toning of facial and neck muscles.

The RMD is proven to firm sagging muscles, increase local blood and lymph circulation, stimulate fibroblast activity, increase the synthesis of new collagen, repair existing collagen and regenerate the homeostasis of skin cells.

The RMD operates with an exclusive Synchronised Treatment Head (STH) that effectively delivers energy to the dermis and muscle tissue, where it safely elicits muscle toning and skin rejuvenation responses.

Authorized for sale by Health Canada under licence no: 90459


The Technologies Behind Our RMD Device

The RMD: STRUCTURAL REMODELING SYSTEM is designed to deliver the most remarkable, non-invasive skin remodelling results in the world of the medical esthetics. This device makes optimal, safe and effective use of 5 recognized electrotherapy technologies exclusively designed to work in synergy to deliver outstanding results.

The Advantages of Our RMD Device

  • Health Canada cleared Class II Medical Device
  • Clinically-proven, visible results achieved within 2 to 8 treatments
  • Non-invasive, safe, effective and efficient
  • Designed and manufactured in Canada in compliance with the highest medical standards
  • Proprietary programmed integration of technologies


Technical information

TÜV CERTIFIED* AND HEALTH CANADA cleared medical device
Universal Power Supply: 120/230 V~, 60/50 Hz
Fuse Type: T1.5 AL (120/230 V~)
Applied Parts Degree of Protection: Type BF
Operating Mode: Continuous
Current Consumption: 1.0 A
Protection Class: 1 (Grounded)
Tolerance / Accuracy of display : ± 15 %
Acoustic Output Frequency: 3 MHz continuous sine wave
Maximum Acoustic Output Power: 4.32 W
Maximum Acoustic Power Density : 0.35 W/ cm
Effective Radiating Area 12.5 cm
BNR 0.07
Beam Type Divergent
Water-ingress Rating IPX7
Maximum HVPC Signal Amplitude: 135 V p-p
HVPC Signal Durations: 60-90-120 μs
Maximum Micro Currents: 3000 μA
Micro Currents Carrier Frequency: 187.5 Hz
Equipment Construction: Internal steel frame
Kydex body
Electronics: Microprocessor controlled
Hand-held Accessories: a Piezoelectric actuator
Ambient Operating Temperature : +10 °C to + 40 °C
Ambient Operating Humidity: 30 % to 75 % RH
Ambient Operating Atmospheric Pressure: 700 hPa to 1060 hPa
Tested to comply to the applicable standards and equipment
specifications:<br />IEC 60601-1-2:2007-(Ed3.0)
ICES-003 Issue 4:2004 / FCC Part 15 Subpart B 15:2010
IEC 60601-1-2:2007-(Ed 3.0) Group 1, Class A
CAN/CSA C22.2 No. 60601-1:2008 excluding Biocompatibility
(clause 11.7), Usability (clauses 7.1.1, and 12.2), PEMS (clause 14),
and EMC clauses and 17).
CAN/CSA C22.2 No. 60601-2-5:2011 excluding EMC (clause 17)
UL 60601-1:2003 excluding EMC (Clauses 6.8.2, and 36),
Biocompatibility (Clause 48), and PEMS
(clause 52.1 as it pertains to IEC 60601-1-4).
IEC 60601-2-5:2000 excluding EMC (clause 36)
ANSI/AAMI ES 60601-1/A2:2010 excluding Biocompatibility (clause
11.7), Usability (clauses 7.1.1, and 12.2), PEMS (clause 14), and
EMC (clauses and 17).
IEC 60601-2-5:2009 excluding EMC (clause 17)
Unit Dimensions*:
Width: 15 in (381 mm)
Height: 9 in (229 mm)
Depth: 21 in (535 mm)
Unit Weight: 10 lb (4.5 kg)
*(without column)