Description
CareFusion Refurbished Alaris LVP Infusion Pump
CareFusion Refurbished Alaris LVP Infusion Pump The increased use of advanced information technologies in the hospital environment promises improved access to and awareness of patient history and treatment plans at all levels of the patient care process. The skillful use of this data can provide an opportunity to improve an enterprise’s clinical, operational and financial performance.
Alaris IV Pump Features
The BD CareFusion Alaris IV Pump Module is used in the delivery of large volume fluids, medications, blood, and blood products using continuous intermittent delivery for adult, pediatric, or neonatal patients. Infusion delivery can occur via clinically acceptable routes of administration (e.g., intravenous, intra-arterial, subcutaneous, epidural, enteral, or irrigation of fluid spaces).
Clinicians can attach up to four pump modules to a single Point of Care (PC) unit allowing four different infusions. The Alaris 8100 modules can be attached to either side of the PC unit to create the desired configuration.
The Alaris 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.
- Alaris 8100 Module has LCD which displays the drug or IV fluid name, dose, and rate.
- Module has indicators which 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
Alaris Pump Specifications
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
- 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:
- Pumping 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)
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