BD Alaris Pump Module 8100

BD Alaris IV Pump Module 8100

The BD Alaris Pump Module 8100 is designed to deliver large volumes of fluids, medications, blood, and blood products using either continuous or intermittent infusion for adult, pediatric, or neonatal patients. It supports various clinically acceptable routes—including intravenous, intra-arterial, subcutaneous, epidural, enteral, and even irrigation—making it a versatile solution in any clinical setting. Up to four pump modules can be attached to a single Point of Care (PCU) Unit, allowing for simultaneous, multi-infusion therapy, with the modules configurable on either side of the PCU to suit your workflow.

Integrated with the Guardrails Suite MX software, the system helps reduce medication errors by testing the reasonableness of programmed parameters before therapy begins. The built-in LCD display shows the IV fluid name, dose, and rate, while color-coded indicators (red for alarm, yellow for pause, and green for infusing) provide clear status updates. With set-based free-flow protection via SmartSite needle-free valves, the pump is designed for bag, bottle, or syringe delivery and supports both primary and secondary (piggyback) infusions.

Specifications:

• Dimensions:

  • Height: 8.9 in (22.6 cm)
  • Width: 3.3 in (8.4 cm)
  • Depth: 5.5 in (14 cm)
  • Weight: 2.5 lb (1.13 kg)

• Air Window & Bolus Settings:

  • Air Detection: Configurable settings allow for a single bolus setting of 50 (with a 2.8 mL volume window and alarm if air exceeds 10%), 75 (8.0 mL window, 20% air alarm), 250 (8.0 mL window, 30% air alarm), or 500 (12.0 mL window, 30% air alarm).
  • Maximum Bolus Volume After Occlusion:
    • At 50 mmHg and a rate of 25 mL/hr: 0.3 mL
    • At 525 mmHg and a rate of 25 mL/hr: 0.6 mL
  • Critical Volume: Maximum over-infusion in a fault condition is 0.6 mL.

• Protection & Pressure:

  • Fluid Ingress Protection: IPX1 (drip proof)
  • Maximum Infusion Pump Pressure: 654 mmHg (accounting for the maximum occlusion alarm threshold plus tolerance)
  • Occlusion Pressure Settings: Adjustable in selectable modes—either preset or user-selectable from 50 to 525 mmHg in 25 mmHg increments.
  • Air-in-Line Detection: Ultrasonic detection with selectable maximum single bolus sizes.

• Performance & Accuracy:

  • IV Pump Rate Accuracy: ±5% at rates between 1 and 999 mL/hr; ±5.5% at rates below 1 mL/hr, under standard test conditions (ambient temperature of 68 ±4°F, source container 20 inches above the top, distilled water, 18-gauge needle, Administration Set Model 2210).
  • Infusion Rate Range: 0.1 to 999 mL/hr
  • IKVO (Keep Vein Open) Rate: Default is 1 mL/hr if the set rate is 1 mL/hr or above, or the set rate if 0.9 mL/hr or below; configurable from 0.1 to 20 mL/hr in 0.1 mL/hr increments.

• Operating Principle & Safety:

  • Operating Principle: Positive displacement
  • Shock Protection: Type CF, defibrillator proof
  • Environmental Operating Conditions:
    • Temperature: 41 to 104°F (5 to 40°C)
    • Relative Humidity: 20 to 90%
    • Atmospheric Pressure: 525 to 4560 mmHg (700 to 6080 hPa)
  • Storage/Transport Conditions:
    • Temperature: -4 to 140°F (-20 to 60°C)
    • Relative Humidity: 5 to 85%
    • Atmospheric Pressure: 375 to 760 mmHg (500 to 1013 hPa)