BodyGuard 575 Pain Management Piston Infusion Pump

CME Medical BodyGuard 575 Pain Management Piston Infusion Pump
Request a Quote


A pain management system with a high degree of flexibility. Blue colour-coded to clearly denote the intended use in opioid analgesic delivery.

Features and benefits

  •  Lightweight and compact, suitable for both bedside and ambulatory use
  •  Piston pump mechanism – ensures unparalleled accuracy and linearity of infusion, even at lowest rates to meet the standards of the most demanding specialties
  •  26 configurable protocols provides storage of drug therapie
  •  Configurable modes of operation which can be set to patients understanding or specialty, bolus only, basal and bolus, basal only
  •  Adjustable air-in-line detection. Cumulative ultrasonic counter, set according to local protocols
  • Variable occlusion pressure settings, configurable to the route of infusion/patient type
  • Bolus configurable up to 1000ml/h, ideal for the delivery of short acting pain relief medication
  • Bolus delivery and infusion rate limiter (hard and soft limits) allows local parameters to be set on the protocols
  • Rechargeable Li-polymer battery and pole mounted mains charger allowing greater flexibility
  • Automatic bolus rate adjustment which optimises bolus delivery and prevents false occlusion alarms


Device type Piston Pump
Basal rate 0.0 to 30.0ml/h in 0.1ml increments
Bolus rate range 40 to 1000ml/h
Priming rate Range 300 to 425ml/h (default 400ml/h)
Total infused volume 9999ml
Bag volume 0.1 to 1000ml
Pump accuracy ± 5%
KVO Rate 0 to 5ml/h
Air sensor Ultrasonic, adjustable air bubble size
Maximum pressure 10psi adjustable (High = 10psi, Normal = 7.5psi, Low = 5psi)
Power supply 110 to 240VAC, 50/60Hz. 0.3A max
Battery Rechargeable Li-Polymer 7.4 volt, 1800mAh
Battery operation 16 hours @ 125ml/h (Rechargeable)
Battery charging Automatic when clicked into the charger connected to an AC power source. Six hours needed to charge a fully depleted battery
Alarms When a problem is detected, the BodyGuard displays the following alarms: Air-in-Line – Down Occlusion – Pump Unattended – End Program – Low Battery – End Battery – Door Open – Error (followed by error code) – Lock Mode – Missing KeyBodyGuard
Dimensions 112 x 89 x 32mm (L x W x H)
Classification Type CF Equipment, degree of protection against electrical shock Class II equipment, IPX3 protection against ingress of water
Housing ABS (fire retardant)
Weight 280g without battery, 390g with battery
Electrical Safety Complies with IEC 60601-1 (Medical Electrical Equipment Safety), IEC601-2-24 (Infusion pumps and controllers), IEC 601-1-4 (Programmable Electrical Medical System) Standards Manufactured in accordance to ISO 9001:2008 and ISO 13485:2003. CE marked in accordance with the Medical Devices Directive 93/42/EEC EMC The BodyGuard infusion system is designed to be in compliance with EN60601-1 (safety) and IEC 601-1-2 (EMC)
Environmental Specifications Non Operating Conditions (Transportation and Storage): Temperature: -25ºC to 50ºC (-13ºF to +122ºF); Humidity: 5% to 100% R.H, non-condensing; Air Pressure: 48kPa to 110kPa Operating Conditions The system may not meet all performance specifications if operated outside of the following conditions: Temperature: +18ºC to +45ºC (+59ºF to +113ºF); Humidity: 20% to 90% R.H at +40ºC, non-condensing; Air Pressure: 70kPa to 110kP Administration set Dedicated administration set