BodyGuard 595™ Regional Analgesia Infusion Pump

The BodyGuard 595™ Regional Analgesia Infusion Pump is a dedicated, colour-coded pain management system for enhanced recovery wound infiltration and nerve blocks, offering a Dose Error Reduction System (DERS). It has a potential library of 26 protocols which can be set up to the patients needs or pain management speciality in hospital or homecare environments.

Key Features

  • Lightweight and compact, suitable for both bedside and ambulatory use.
  • Configurable modes of operation which can be set to patients needs or clinical specialty; continuous only, bolus only continuous plus bolus and auto bolus.
  • Automatic bolus rate adjustment optimises bolus delivery and prevents false occlusion alarms.
  • The Post-Occlusion Bolus Reduction System will safely release pressure from the line, following an occlusion, without administering a potential post-occlusion bolus.

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Main Features

  • Lightweight and compact, suitable for both bedside and ambulatory use.
  • The BodyGuard pumping mechanism ensures outstanding accuracy and linearity of infusion, even at lowest rates to meet the standards of your most demanding specialties.
  • 26 configurable medication protocols provide storage of drug therapies and limit set up time.
  • Configurable modes of operation which can be set to patients needs or specialty; continuous only, bolus only continuous plus bolus and auto bolus.
  • Adjustable air-in-line detection and occlusion pressure settings help to protect patients by providing a fast time to alarm, ensuring early detection of potential issues.
  • Rechargeable Li-Polymer battery and pole mounted mains charger allow greater flexibility.
  • Automatic bolus rate adjustment optimises bolus delivery and prevents false occlusion alarms.

Safety Features

  • MediGuard™ weight-based dosing software will automatically set a toxicity ceiling based on your patient’s weight, to prevent excess drug delivery.
  • The built-in event log automatically records accurate and reliable data on pump use.
  • The lockable keypad prevents inadvertent key presses.
  • Fixed or variable code protected programmes are accessible only by authorised personnel.
  • The Post-Occlusion Bolus Reduction System will safely release pressure from the line, following an occlusion, without administering a potential post-occlusion bolus.
  • A range of alerts and alarms will draw immediate attention to any pump status requiring intervention.
  • Pump event log accessible via INFO MENU or downloaded to PC through BodyComm software

Accessories

  • 170-000X: BodyGuard 100ml Lockbox + 2 Keys
  • 170-250X: BodyGuard 250ml Lockbox + 2 Keys
  • 190-900PXCVM: BodyGuard Ultimate ColourVision 500ml Lockbox + 4 Keys
  • 150-000X: Carry Pouch 100ml
  • 150-001X: Carry Pouch 250ml/500ml
  • 150-250XD: BodyGuard 250ml Single Use Grey Carry Pouch
  • 141-100XM: Remote Bolus Button - Coded
  • 130-050X2: Battery Cell X2 9V
  • 130-050XA: BodyGuard Classic Standard Life Battery 1800mAh
  • 130-051X: BodyGuard Classic Extended Life Battery 3600mAh
  • 150-314X: BodyGuard Charger LED and DC
  • 150-331X: External Battery Charger
  • 150-314XM: BodyGuard Charger - No Display
  • 196-000X: Battery Charging Cable (DC Cable)
  • 100-072XA: 13a Plug Lead 1.8m (Straight)
  • BODYCA: Bodycomm Kit for BodyGuard

Consumables

  • 100-160XSM: Clear Microset With SR Segment and 90° Angled Spike
  • 100-160XSMG90EK: Extended Administration Set With Grey Tubing and 90° Angled Spike

Technical Specification

Device type Piston pump
Flow rate 0.0 to 100ml/h in 0.1ml increments
Priming rate Range 300 to 435ml/h (default 400ml/h)
Total infused volume 0.1 to 1,000ml
Pump accuracy +/- 5%
KVD rate 0 to 50ml/h
Air sensor Ultrasonic, adjustable air bubble size
Maximum pressure 35 psi adjustable (High = 28psi/High2 = 28psi/High3 = 35psi, Normal = 14psi, Low 7psi
Power supply 110 to 240 VAC, 50/60 Hz 0.3A max
Battery Rechargeable LI-Polymer 72 volt, 1800mAh
Battery operation 20 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 and alerts When a problem is detected, the BodyGuard displays the following alarms - air in line, down occlusion, pump unattended, end program/near end (alert), low battery (alert), end battery, door open, error (followed by error code), lock mode, missing key
BodyGuard 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 ISO9001;2008 and ISO13485;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 IEC601-1-2 (EMC)
Environmental specifications Non Operating Conditions (Transportation and Storage)
Temperature -25°C to 50°C (-13°F to +122°F)
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 +18°C to +45°C (+59°F to + 113°F)
Humidity 20% to 90% R.H. at +40°C, non-condensing
Air pressure 70kPa to 110kPa
Administration set - dedicated administration set with anti-siphon valve and key

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