CME Infusion Infusion Pump | BodyGuard ...

CME Infusion - Infusion Pump | BodyGuard ColourVision 575

Supplier: BD Australia

Infusion Pump | BodyGuard ColourVision 575

The BodyGuard ColourVision 575™ PCA Infusion Pump is a dedicated, colour-coded pain management system, for Patient Controlled Analgesia (PCA) infusions offering a Dose Error Reduction System (DERS).

In Stock

Applications for this product

Acute pain management

Features of this product

MediGuard™ weight-based dosing software, MediGuard™ weight-based dosing software will automatically set a toxicity ceiling based on your patient’s weight, to prevent excess drug delivery
Pressure displayed, Actual pressure displayed on the main screen allows close monitoring of real-time in-line pressure
Built-in event log, The built-in event log automatically records accurate and reliable data on pump use
Lockable keypad, The lockable keypad prevents inadvertent key presses
Code protected programmes, Fixed or variable code protected programmes are accessible only by authorised personnel
Post-Occlusion Bolus Reduction System, The Post-Occlusion Bolus Reduction System will safely release pressure from the line, following an occlusion, without administering a potential post-occlusion bolus
Pump event log, Pump event log accessible via INFO MENU or downloaded to PC through BodyComm software

Specifications of this product

We have various models and specifications in our range. These details are for the Infusion Pump | BodyGuard ColourVision 575. Get in touch to let us know your requirements so we can quote you on a product that best suits your needs.

Pumping Mechanism: Piston pump
Flow Rate: 0 to 30 ml/hr in 0.1ml increments
Priming Rate: 300ml/hr to 425ml/hr (default 400ml/hr)
Total Infused Volume: 0.1 to 1,000 ml
Total Time Setting: 100 hours
Accuracy: +/- 5%
KVO rate: 0.1 to 5 ml/hr
Air Sensor: Ultrasonic, adjustable air bubble size
Maximum Pressure: 10 psi Adjustable (250mmHg - 520mmHg (5psi - 10psi ))
Power Supply: 110-240 VAC, 50/60 Hz. 0.3A max
Battery: Rechargeable Li-Ion 7.4V, 1800mAh. (Typical)
Battery Operation at 125 ml/hr: 15 hours (Rechargeable)
Battery Charging: Automatic when clicked into the Charger that is connected to an AC power source. Six hours needed to charge a fully-depleted battery.
Alarms: air in line, down occlusion, pump unattended, end of infusion, low battery, end battery, door open, error (followed by error code), lock mode, lock out mode, missing key
Dimensions: 112 x 89 x 32mm. (L x W x H)
Classification: Type CF Equipment (degree of protection against electrical shock)
Housing: PCABS (fire retardant)
Weight: 280g without battery, 390g with battery
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)
Standards: Manufactured in accordance with ISO 900; 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 EN 60601-1 (safety) and IEC 601-1-2 (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 sets - dedicated administration sets with anti-siphon valve.

To contact BD Australia about CME Infusion Infusion Pump | BodyGuard ColourVision 575 use Get a quote.

Applications for this product

Acute pain management

Features of this product

MediGuard™ weight-based dosing software, MediGuard™ weight-based dosing software will automatically set a toxicity ceiling based on your patient’s weight, to prevent excess drug delivery
Pressure displayed, Actual pressure displayed on the main screen allows close monitoring of real-time in-line pressure
Built-in event log, The built-in event log automatically records accurate and reliable data on pump use
Lockable keypad, The lockable keypad prevents inadvertent key presses
Code protected programmes, Fixed or variable code protected programmes are accessible only by authorised personnel
Post-Occlusion Bolus Reduction System, The Post-Occlusion Bolus Reduction System will safely release pressure from the line, following an occlusion, without administering a potential post-occlusion bolus
Pump event log, Pump event log accessible via INFO MENU or downloaded to PC through BodyComm software

Specifications of this product

Pumping Mechanism: Piston pump
Flow Rate: 0 to 30 ml/hr in 0.1ml increments
Priming Rate: 300ml/hr to 425ml/hr (default 400ml/hr)
Total Infused Volume: 0.1 to 1,000 ml
Total Time Setting: 100 hours
Accuracy: +/- 5%
KVO rate: 0.1 to 5 ml/hr
Air Sensor: Ultrasonic, adjustable air bubble size
Maximum Pressure: 10 psi Adjustable (250mmHg - 520mmHg (5psi - 10psi ))
Power Supply: 110-240 VAC, 50/60 Hz. 0.3A max
Battery: Rechargeable Li-Ion 7.4V, 1800mAh. (Typical)
Battery Operation at 125 ml/hr: 15 hours (Rechargeable)
Battery Charging: Automatic when clicked into the Charger that is connected to an AC power source. Six hours needed to charge a fully-depleted battery.
Alarms: air in line, down occlusion, pump unattended, end of infusion, low battery, end battery, door open, error (followed by error code), lock mode, lock out mode, missing key
Dimensions: 112 x 89 x 32mm. (L x W x H)
Classification: Type CF Equipment (degree of protection against electrical shock)
Housing: PCABS (fire retardant)
Weight: 280g without battery, 390g with battery
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)
Standards: Manufactured in accordance with ISO 900; 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 EN 60601-1 (safety) and IEC 601-1-2 (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 sets - dedicated administration sets with anti-siphon valve.