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MultiPort

MultiPort

Product catalog summary
Overview: The BIOFLEX® MultiPort System is designed to operate up to four treatment arrays or laser probes simultaneously, with continuous monitoring displayed on four screens throughout the treatment session.
Inclusions: The system includes a touch screen monitor, two BIOFLEX DUO+240 Treatment Arrays, two laser probes of choice, and two sets of safety glasses.
Features: The system allows treatment of up to four patients simultaneously using any combination of flexible arrays and laser probes. It features an intuitive touchscreen for continuous monitoring and a manual stop button for increased safety. It is described as the most advanced, full-featured Laser Therapy System.
Technical Specifications:
  • Mode of operation: Continuous Wave (CW), Pulsed (Modulated)
  • Waveform: Square
  • Power: 0-100% in 1% steps
  • Duration: 0-3,600 seconds (up to 60 minutes)
  • Frequency: 1-10,000 Hz with 5 μs resolution
  • Duty Cycle: 10-90% in 10% steps with 5 μs resolution
Patents and Approvals: BIOFLEX Systems are manufactured under the ISO 13485:2016 quality system. They are authorized for sale by Health Canada and registered with the FDA as a medical device. The systems are approved for marketing in Canada under a Health Canada Medical Device License. Meditech holds patents worldwide, including North America, Europe, and Australia.
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Catalog excerpts

MultiPort-1

MultiPort Professional The BIOFLEX® MultiPort System can operate up to four treatment arrays or laser probes simultaneously. Continuous monitoring is displayed on all four screens throughout the entire treatment. Includes: Touch screen monitor Two BIOFLEX DUO+240 Treatment Arrays Two laser probes of your choice Two sets of safety glasses Features: Treat up to 4 patients simultaneously using any combination of flexible arrays and laser probes Intuitive touchscreen that continuously monitors treatments throughout the entire session Manual stop button for increased safety Our most advanced, full featured Laser Therapy System Technical Specifications Percent of total power Duty Cycle BIOFLEX Systems are manufactured under the ISO 13485:2016 quality system. BIOFLEX MiniPort Systems are authorized for sale by Health Canada and registered with the FDA as a medical device. BIOFLEX systems are approved for marketing in Canada under a Health Canada Medical Device License. Meditech holds patents worldwide, including but not limited to North America, Europe and Australia

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