Alaris/BD CareFusion 8100 Infusion Pump Module - (OLD STYLE)

Out of stock
SKU: EN-ALARIS-8100
Condition
Category
LEAD TIME: Estimated Ship Time: 7-10 Days
PACKAGING: 1
WARRANTY: 6 Months

Listing Terms & Conditions

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The Alaris / BD CareFusion 8100 IV Pump Module plays a crucial role in administering significant quantities of fluids, medications, blood, and blood products to adult, pediatric, or neonatal patients. It utilizes a continuous intermittent delivery method to ensure precise and controlled infusion. This module allows for infusion delivery through various clinically approved administration routes, including intravenous, intra-arterial, subcutaneous, epidural, enteral, or irrigation of fluid spaces.

Clinicians have the capability to connect a maximum of four pump modules to a singular Point of Care (PCU) Unit, which enables the administration of four distinct infusions concurrently. The Alaris 8100 modules offer flexibility in their attachment to either side of the PC unit, thereby facilitating the creation of the desired configuration as per the clinician's requirement.

The Alaris / BD Carefusion 8100 module supports the Guardrails Suite MX software. This software helps to reduce the risk of medication errors by providing a test of reasonableness before the initiation of therapy.

FEATURES:

  • LCD which displays the drug or IV fluid name, dose, and rate.
  • Indicators that display channel status-red for alarm, yellow for pause, and green for infusing.
  • Set-based, free-flow protection featuring the SmartSite needle-free valves.
  • Sets can be used for gravity infusion.
  • Designed for bag, bottle, or syringe delivery.
  • Supports primary and secondary “piggyback” delivery

SPECIFICATIONS:

  • Manufacturer: Alaris/BD Carefusion
  • Part Number: (OEM): 8100
  • Category: Infusion Pump Modules
  • Accessories: None
  • Condition: Refurbished
  • Weight: 2.5 lb.
  • Warranty: 6 Months
  • Dimensions:
    • Height: 8.9” (22.6 cm)
    • Width: 3.3” (8.4 cm)
    • Depth: 5.5” (14 cm)
    • Weight: 2.5 lbs (1.13 kg)
  • Accumulated Air Window:
    • Single Bolus Setting: 50; Volume Window (mL): 2.8; Air That Causes Alarm: 10%
    • Single Bolus Setting: 75; Volume Window (mL): 8.0; Air That Causes Alarm: 20%
    • Single Bolus Setting: 250; Volume Window (mL): 8.0; Air That Causes Alarm: 30%
    • Single Bolus Setting: 500; Volume Window (mL): 12.0; Air That Causes Alarm: 30%
  • Bolus Volume, Maximum After Occlusion:
    • Pressure Limit (mmHg): 50; Rate (mL/h): 25; Bolus Volume (mL): ≤0.3
    • Pressure Limit (mmHg): 525; Rate (mL/h): 25; Bolus Volume (mL): ≤0.6
  • Critical Volume:
    • The maximum over-infusion which can occur in the event of a single fault condition is 0.6 mL.
  • Fluid Ingress Protection:
    • IPX1, Drip Proof
  • Maximum Infusion Pressure:
    • 654 mmHg (Maximum Occlusion Alarm Threshold plus tolerance)
  • Rate Accuracy:
    • ±5% at rates between 1 and 999 mL/h; ±5.5% at rates <1 mL/h, 95% of the time with 95% confidence, under the conditions listed below.
    • Infusion Rate Range: 0.1 - 999 mL/h
    • Ambient Temperature: 68 ±4° F (20 ±2° C)
    • Source Container Height: 20 inches above top of Pump Module
    • Test Solution: Distilled Water
    • Distal Back pressure: 0 mmHg (0 kPa)
    • Needle: 18 gauge
    • Administration Set Model: 2210
  • Infusion of Air, Means to Protect Patient From:
    • Ultrasonic Air-in-Line Detection: Maximum single bolus size = selectable 50, 75 or 250 microliters nominal (500 microliters in Anesthesia Mode)
  • IKVO (Keep Vein Open) Rate:
    • Factory Default Setting is 1 mL/h if set rate is 1 mL/h or above; or set rate, if rate is 0.9 mL/h or below.
  • KVO Selection Range:
    • KVO rate can be set in System Configuration from 0.1 - 20 mL/h in 0.1 mL/h increments.
  • Occlusion Alarm Thresholds:
    • Pump Mode: 525 mmHg at rates ≥30 mL/h Varying level based on rate and patient back–pressure at rates <30 mL/h.
    • Selectable Mode: User selected, 50 - 525 mmHg in 25 mmHg increments.
  • Operating Principle:
    • Positive displacement
  • Shock Protection:
    • Type CF, Defibrillator Proof
  • Environmental Operating:
    • Temperature Range: 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:
    • Temperature Range: -4 to 140°F (-20 to 60°C)
    • Relative Humidity: 5 to 85%
    • Atmospheric Pressure: 375 to 760 mmHg (500 to 1013 hPa)

    In addition, please acknowledge the following disclaimer:

    * IMPORTANT - PLEASE READ BEFORE PURCHASING! * All pictures of items being sold are used for reference purposes and are described as accurately as possible. If there is an error in a listing, we will try and resolve any issues to the best of our abilities that may arise before or after a sale. Complete units all come with a power cord and DO NOT come with any cables, sensors, manuals, accessories etc. unless otherwise noted in the description.

    Purchaser agrees that seller is not liable for any injuries or damages of any kind associated in any way with this equipment. Purchaser agrees to indemnify and hold harmless seller and seller's officers, directors, employees, agents, and shareholders against any and all claims, liabilities, obligations, demands, cost and expenses of every kind and nature, including but not limited to attorney's fees and litigation expenses, from or related to the equipment and any use thereof.

    * NOTE - FDA Regulation and Certification: "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, we will verify your status as an authorized purchaser of this item before shipping of the item."

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