Technology

Made to medical specifications

Body Boost Bed is used in Sport’s Rehabilitation centers, Hospital and Clinical settings. Med-Spas, Day Spas, and also for private use. The device is fully automated with a touch screen above the patient allowing easy device management, minimizing medical staff engagement throughout therapy application. Body Boost Bed (BBB Med S9001) is a light therapy device that uses blue (470 nm), red (630 nm) and near infrared (940 nm) LED light for medical treatment of muscular and joints related pain, micro-circulation disorders and Anti-Ageing.

Accessibility

Body Boost Bed is designed with a Contoured Base for maximum easy access and enables patients with in a different health states to slide easily in and out of the Body Boost Bed unassisted. The base of the bed is contoured to mimic the body's curves and it's ergonomically designed for comfort.

Certificates

CE Certified Medical Device

Medical grade power supply

ISO 13485:2016 Quality Management System

Technical specifications

Bed diagram
Bed diagram

Dimensions

  • Width 230 cm
  • Height 155 cm
  • Depth 100 cm
  • Weight 210 kg

Wavelength

  • Blue: 470 nm
  • Red: 630 nm
  • Near-infrared: 940 nm
  • Pulsed Multi frequencies system

Power requirements

  • TDP: 1,500 W
  • Outlet: 220–240 VAC
  • Fuse: 10 A

Regulatory

Full list of the standards that our product is manufactured in accordance to:

EN 60601–1:2006 +A1:2013 +A12:2014 +AC:2014

Medical electrical equipment. General requirements for basic safety and essential performance

EN 60601–1-2:2015

Medical electrical equipment. General requirements for basic safety and essential performance. Collateral Standard. Electromagnetic disturbances. Requirements and tests.

EN 60601–1-6:2010+A1:2015

Medical electrical equipment. General requirements for basic safety and essential performance. Collateral standard. Usability

EN 62366–1:2015+AC:2015

Medical devices. Application of usability engineering to medical devices.

EN 62471:2008

Photobiological safety of lamps and lamp systems

EN ISO 13485:2016

Medical devices. Quality management systems. Requirements for regulatory purposes.

EN ISO 14971:2012

Medical devices. Application of risk management to medical devices.

EN ISO 10993-1:2009+AC:2010

Biological evaluation of medical devices. Evaluation and testing within a risk management process

EN ISO 10993-5:2009

Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity.

EN ISO 10993-10:2009

Biological evaluation of medical devices. Tests for irritation and delayed-type hypersensitivity

EN ISO 15223–1:2016

Medical devices — Symbols to be used with medical device labels, labeling and information to be supplied