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
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