BodyGuard 2CH™ Twin Channel Infusion Pump

The BodyGuard 2CH™ Twin Channel Infusion Pump is an ambulatory multi-therapy pump suitable for hospital and homecare environments with five infusion programs, (Continuous, Dose, 25 step, TPN and Intermittent).

Key Features

  • Designed to be intuitive to program and use
  • Configurable modes of operation which can be set to a speciality or patient's understanding - TPN, continuous, multi-step, intermittent and dose
  • Adjustable air-in-line detection. The cumulative ultrasonic counter can be set according to local protocols
  • Variable occlusion pressure settings, configurable to the route of infusion/patient type

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Main Features

  • The piston pump mechanism ensures unparalleled accuracy and linearity of infusion, even at lowest rates to meet the standards of the most demanding specialities
  • Configurable modes of operation which can be set to a speciality or patients understanding - TPN, continuous, multi-step, intermittent and dose
  • Adjustable air-in-line detection. The cumulative ultrasonic counter can be set according to local protocols
  • Variable occlusion pressure settings, configurable to the route of infusion/patient type
  • A delayed start infusion option means no reminder and no additional clinical intervention needed once pump has been set up for general infusion
  • Designed to be intuitive to program and use

Safety Features

  • Built-in event log automatically records accurate and reliable data on pump use
  • Lockable keypad to prevent inadvertent key presses
  • Fixed or variable code protected programmes that are configured and locked into the pump memory and can only be accessed by authorised personnel or technicians
  • Post Occlusion Bolus Reduction System will safely release pressure from the line, following an occlusion, without administering a post occlusion bolus
  • Pump event log accessible via INFO MENU or downloaded to PC through BodyComm software

Accessories

  • 160-001X: Blue 3 Litre Rucksack
  • 160-002XB: Black 2 Litre Rucksack
  • 160-002XG: Grey 2 Litre Rucksack
  • 160-002XP: Pink 2 Litre Rucksack
  • 150-313T: BodyGuard 2CH Charger with LED
  • 100-072XA: 13a Plug Lead 1.8m (Straight)

Consumables

  • 120-112XSFV: Microset With 1.2 Filter SR Segment and Priming Valve
  • 120-160XSFM: Microset With 0.2 Filter SR Segment and Blue Valve
  • 100-160XSM: Clear Microset With SR Segment
  • 120-163XBS: BodyGuard Burette Administration Set
  • 120-160XSV: Clear Microset With No Filter, NDEHP, clear with SR segment

Technical Specification

Description Piston mechanism, ambulatory infusion pump with two independent channels. The pump can be used for ambulatory care in a rucksack or mounted into a charger unit. Pole mounted charging unit available (with or without the large infusion status display).
Software Version TwinTPN_03
IV Administration set Dedicated IV administration sets, with anti-siphon valve to prevent free flow
Flow Rate 0.1ml/h to 100ml/h in 0.1ml/h increments and 100ml/h to 1,200ml/h in 1ml/h increments
Volume Accuracy +/- 5%
Adjustable Occlusion Pressure Settings Eight alarm levels available and the default is, Level 6 (480mmHg). Level 1 = 60mmHg, Level 2 = 90mmHg, Level 3 = 150mmHg, Level 4 = 240mmHg, Level 5 = 360mmHg, Level 6 = 480mmHg, Level 7 = 720mmHg, Level 8 = 990mmHg
Pressure Accuracy +/-155mmHg (+/-3psi)
Air Sensor Ultrasonic, adjustable air bubble size. Air-in-line accumulation and single bubble detection
Air-in-line limits 0.04ml to 2ml
Priming Rate 100ml/h to 1,200ml/h in 1ml/h increments
KVO rate Rate (max)
Stand-by Time (pump paused) 2min (before 'Pump Paused Too Long' alarm sounds)
Total Time Setting 99hrs 59min
Modes of Operation - Total Parenteral Nutrition (TPN) The program has a taper up/taper down pattern. The parameters to be set are Total Volume, Time Up, Time Down and Total Time. The pump will calculate the infusion rates required
Volume To Be Infused 0.1ml to 6,553ml
Total Time 00;01 to 99;59
Up Time 00;00 to 04;15
Down Time 00;00 to 04;15
Total Volume Infused 0.1ml to 9,999ml
Modes of Operation - Continuous User can program a Rate or Volume Over Time. Infusion rate 0.1ml/h to 100ml/h in 0.1ml/h increments and 100ml/h to 1,200ml/h in 1ml/h increments
Volume To Be Infused 0.1ml to 6,553ml
Time 1min to 99hrs 59min in 1min increments
Total Volume Infused 0.1ml to 9,999ml. Including Secondary infusion (see below)
Modes of Operation - 25 Steps User can design a specific protocol for drug delivery which contains up to 25 steps by rate/volume/time. Infusion rate 0.1ml/h to 100ml/h in 0.1ml/h increments and 100ml/h to 1,200ml/h in 1ml/h increments
Total Volume Infused (per step) 0.1ml to 9,999ml
Accumulated Total Volume Infused (for all steps) - up to 10L
Modes of Operation - Intermittent User can design a specific protocol for drug delivery which can be delayed for a period of time
Total Volume Infused 0.1ml to 6,553ml
Dose Volume To Be Infused 0.1ml to 6,553ml
Dose Rate 0.1ml/h to 100ml/h in 0.1ml/h increments and 100ml/h to 1,200ml/h in 1ml/h increments
Interval Time 00;01 to 72;00. KVO 0ml/h to 5ml/h in 0.1ml/h increments
Modes of Operation - Dose User can program a dose based infusion in either µg/kg/min or mg/kg/min
Patient Weight 0.1kg to 99.9kg in 0.1kg increments and 100kg to 250kg in 1kg increments.
Drug Concentration 0.01mg/ml to 9.99mg/ml in 0.01mg/ml increments and 10.0mg/ml to 99.9mg/ml in 0.1mg/ml increments and 100mg/ml to 500mg/ml in 1mg/ml increments.
Dose 0.01µg/kg/min to 9.99µg/kg/min in 0.01µg/kg/min increments and 10.0µg/kg/min to 99.9µg/kg/min in 0.1µg/kg/min increments and 100µg/kg/min to 327µg/kg/min in 1µg/kg/min increments (maximum dose limited by the maximum rate setting); 0.01mg/kg/min to 9.99mg/kg/min in 0.01mg/kg/min increments and 10.0mg/kg/min to 99.9mg/kg/min in 0.1mg/kg/min increments and 100mg/kg/min to 327mg/kg/min in 1mg/kg/min increments (maximum dose limited by the maximum rate setting).
Volume To Be Infused 0.1ml to 6,553ml
Secondary Infusion Secondary infusion (Piggy back) programmable with the same infusion rate and volume capabilities as the default programme. User can titrate the Secondary Infusion with the same method that is used for a primary continuous infusion. Available in Continuous mode only
Keypad Locking During operation, all keys are disabled excluding the STOP/NO and INFO key.
Programme Locking Enables the operator to lock out the setting keys, so that entered parameters and set programs cannot be changed once they are set.
Maximal Rate Locking Enables the operator to set a maximum rate for the pump. The programmable rate can be adjusted only up to the pre-set limit
Alerts Low battery program, nearly complete
Alarms/notifications air/upstream occlusion, down occlusion, door open, pump paused too long (un-attended), end program, end battery, missing key, restart pump, system/technical problem, wrong TPN data, lock mode, fatal error
Alarm volume Range 0 to 7; 4 (min) and 7 (max)
LED Indicator ON/OFF (Default= OFF)
Event Log Date and time stamped pump event history (last 512 events visible)
Computer Interface PC BodyComm communications (RS232) with charger (docking station). For servicing, pump programming and event log viewing and printing
Battery Life 7.5hrs infusing @ 125ml/h (both channels infusing simultaneously)
Mains and Battery Power Supply AC mains power 110-240VAC, 50/60Hz. 0.3A max
Battery Rechargeable, Li-Polymer, 7.4V, 1800mAh (typical)
Battery Charging Battery charging commences automatically when the pump is mounted into the charger unit (docking station) that is connected to an AC Mains source. (LED confirmation of AC Mains connected)
Battery charging time 6hrs (to charge a fully depleted battery)
Pump Dimensions Pump - 89mm (height) x 149mm (width) x 41mm (depth)
Pump with charger (docking station) - 127mm (height) x 155mm (width) x 84mm (depth),
Charger (docking station) - 127mm (height) x 155mm (width) x 57mm (depth)
Weight Pump with battery - 551g
Pump with charger (docking station) - 1,018g
Charger (docking station) - 467g
Degree of protection against fluid ingress IPX1
Housing ABS (fire retardant)
Degree of protection against electrical shock Type CF Equipment
Electrical Safety Complies with, EN 60601-1 (Medical Electrical Equipment Safety), IEC 60601-2-24 (Infusion Pumps and Controllers), IEC 60601-1-4 (Programmable Electrical Medical System), UL 2601- 1 and CAN/CSA C22.2 No 601.1
Standards Manufactured in accordance with ISO 9001;2008 and ISO 13485;2003 CE marked (in accordance with the Medical Devices Directive 93/42/EEC) Electromagnetic Compatibility (EMC) EN 60601-1 (safety) and IEC 60601-1-2 (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 +15°C to +40°C (+59°F to +104°F)
Humidity 20% to 90% R.H. at +40°C, non-condensing
Air pressure 70kPa to 110kPa

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