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, freeflow 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
Features & 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 lbs (1.13 kg) |
Other
| Accumulated Air Window: |
|
| Bolus Volume, Maximum after Occlusion: |
|
| 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: |
|
| Infusion of Air, Means to Protect Patient: | 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: |
|
| Operating Principle: | Positive displacement |
| Shock Protection: | Type CF, Defibrillator Proof |
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) |
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, freeflow 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 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) Warranty:
For new products, please refer to the manufacturer's website for details.
This product has been refurbished and tested to the highest quality standards by The PCB Medical. This Limited Warranty offered by PCB Medical covers defects in material or workmanship. This warranty extends to the original purchaser only and is nontransferable. The warranty begins the day the equipment is received. Please inspect your item(s) upon delivery. Any unauthorized service providers working on our equipment within the warranty period will void the warranty!
Our warranty periods are very based on product, a standard 30 day parts warranty is included with all refurbished parts unless stated otherwise on the quote/Invoice. Warranties begin from the documented date of receipt.
Our warranties do not cover any problem that is caused by: A. Conditions, malfunctions or damage not resulting from defects in material or workmanship. B. Conditions, malfunctions or damage resulting from (1) normal wear and tear, improper installation, improper maintenance, misuse, abuse, negligence, accident or alteration.
Our limited warranties are void if a product is returned with removed, damaged or tampered labels or any alterations (including removal of any component or external cover).
PCB Medical will not provide any warranty coverage unless claims are made in compliance with all terms of the controlling warranty statement included with your product and you follow proper return procedure. To request warranty service, you will need to provide: 1. The invoice or other evidence of the date and place of purchase. 2. A description of the problem. 3. Contact our Customer Service Department to receive a Return Authorization Number (RMA#)
Shipping and Returns:
Damaged freight needs to be reported within 24 hours to file a claim. No merchandise may be returned without prior written authorization by PCB Medical.
No NEW merchandise may be returned unless authorization from manufacturer which could result in a restocking fee or no return at all, and customer is responsible for shipping expenses.
Return period for products is thirty (30) days from delivery or otherwise agreed upon.
The PCB Medical will test returned products returned and can impose a customer fee if the customer misrepresents the condition of the product.
CREDIT AND RETURN SHIPPING GUIDELINES
Order cancellations (after 24 hours) and returns are charged a 45% restocking fee. Damaged goods will receive credit dependent on the condition of the product, and customer is responsible for shipping expenses.
No credit will be issued if the item is non-returnable, such as a new product, custom or special order, or in the case that the item is damaged due to improper handling/packaging by the customer.
Shipping Charges: Customers are responsible for making sure items can be delivered into or outside of their facility without issue. For example, can a 53’ foot truck access your building? Failure to accommodate delivery can result in items not being delivered, additional fees, or return of equipment.
Basic Shipping Charge is for dock to dock shipping and/or liftgate service shipping. The items shipping dock to dock and/or liftgate are skidded/palletized items. It doesn’t not include inside delivery.
Residential shipping charge is for customer’s needing delivery in a residential area.
Inside delivery is for customer’s needing their purchase delivered inside the building. The item(s) will be delivered into the lobby only. They are not delivered into rooms/suites, elevators, or stairs.
Customers are responsible for disposing of packing materials.
If you are needing white glove delivery, please contact us directly at INFO@pcbhme.com
