1. Visual Inspection
Each pump is examined for external damage, cracks, and signs of wear on the body and components. Cosmetic issues and potential safety concerns are noted for further action.
Refurbished Carefusion Alaris 8120 PCA Module
In stock
$1,225.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Syringe-based patient-controlled analgesia (PCA) module for the Alaris modular infusion system
- Flow rate 0.1–999 mL/h • ±2% rate accuracy excluding syringe variation
- Four operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only • clinician-programmed bolus dose also supported
Refurbished CareFusion Alaris 8120 PCA Module
Refurbished • 1-Year Warranty • Model 8120 syringe-based patient-controlled analgesia module for the Alaris modular system
The CareFusion Alaris 8120 PCA Module is a syringe-based patient-controlled analgesia module designed for facilities that use syringe pumps to deliver medications or fluids. It supports adult, pediatric, and neonatal patients and provides continuous or intermittent delivery through clinically acceptable routes including intravenous, subcutaneous, and epidural administration. The module operates as part of a compatible Alaris System and does not operate as a standalone infusion pump.
What’s Included
- 1× CareFusion Alaris PCA Module, Model 8120
- Dose Request Cord / patient bolus handset included
- Security key(s) for the locking PCA door included
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8120 provides syringe-based PCA functionality within the Alaris modular infusion platform. A locking security door helps control access to the syringe and medication, while the Dose Request Cord allows the patient to request programmed PCA doses when PCA-only or PCA + continuous modes are in use.
The PCA Module supports four manufacturer-defined operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only. A clinician-programmed bolus dose can also be delivered as a separate function after PCA therapy has begun. The PCA Module requires an appropriately configured Alaris System Data Set containing a Drug Library. Guardrails Suite MX then applies facility-defined medication-safety limits and PCA therapy parameters.
- Alaris PCA Module — Model 8120
- Flow rate range: 0.1–999 mL/h, subject to syringe-size restrictions
- Supported flow-rate categories: 20 mL, 30/35 mL, and 50/60 mL; approved syringe models depend on manufacturer and installed PCA Module software
- Rate accuracy: ±2% of full-scale plunger travel, excluding syringe variation
- Three configurable downstream occlusion-pressure settings: Low, Medium, and High
- Optional PCA Pause Protocol can integrate with compatible Alaris SpO2 and/or EtCO2 monitoring modules when configured by the facility
Specifications — CareFusion Alaris PCA Module Model 8120
| Manufacturer | CareFusion |
| Model | 8120 — Alaris PCA Module |
| Type | Syringe-based patient-controlled analgesia (PCA) infusion module |
| System Requirement | Requires a compatible Alaris PC Unit and properly configured Alaris System; does not operate as a standalone pump |
| United Infusion Configuration | Sold for use with the Alaris 8015 PC Unit, sold separately |
| Patient Population | Adult, pediatric, and neonatal patients |
| Intended Delivery | Continuous or intermittent delivery of medications or fluids |
| Administration Routes | Clinically acceptable routes including intravenous (IV), subcutaneous, and epidural administration |
| Operating Modes | PCA Only; Continuous Infusion; PCA + Continuous Infusion; Loading Dose Only |
| Bolus Dose | Clinician-programmed bolus dose available as a separate function during PCA therapy when enabled and permitted by the configured system |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D, exclusive of security door |
| Weight | 5.5 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.10–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| 20 mL Syringe Rate Range | 0.1–500 mL/h |
| 30 / 35 mL Syringe Rate Range | 0.1–650 mL/h |
| 50 / 60 mL Syringe Rate Range | 0.1–999 mL/h |
| Syringe Compatibility | Uses approved single-use disposable luer-lock syringes. Supported flow-rate categories are 20 mL, 30/35 mL, and 50/60 mL. Permitted syringe manufacturer and model combinations depend on PCA Module software version and applicable compatibility documentation. The October 2019 v9.xx addendum confirms compatibility of BD Plastipak 50 mL syringe model 309653, displayed on the Alaris PC Unit as BD Plastipak 50/60 mL. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available syringe-selection list; displayed syringe manufacturer/type and size must be verified before use |
| Rate Accuracy | ±2% of full-scale plunger travel, not including syringe variation |
| Occlusion Alarm Thresholds | Three selectable settings: Low, Medium, and High |
| Occlusion Pressure Set Points | Low: 200 mmHg • Medium: 500 mmHg • High: 800 mmHg |
| Bolus Delivery Rate | Configurable from 75–500 mL/h, limited by syringe size |
| Lockout Interval | 1–99 minutes in 1-minute increments |
| PCA / Loading / Bolus / Maximum Dose Ranges | Configured according to hospital-defined best-practice guidelines through the applicable Drug Library and facility Data Set |
| Patient History | Records and displays up to 24 hours of patient history with selectable 1-, 2-, 4-, 8-, 12-, and 24-hour trend intervals |
| Dose Request Cord | Required for patient-requested PCA dosing in PCA-only and PCA + continuous infusion modes |
| PCA Pause Protocol | Optional hospital-configurable feature; when enabled with compatible SpO2 and/or EtCO2 modules, PCA infusion pauses and alarms when defined monitoring values for low %SpO2 and/or respiratory rate are exceeded and sustained |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part for PCA disposable; Type BF, Defibrillator Proof for Dose Request Cord |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Safety Software | Requires an appropriately configured Alaris System Data Set containing a Drug Library; Guardrails Suite MX applies facility-defined medication-safety limits and PCA therapy parameters |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, the Alaris PCA Module v9 Quick Reference Guide, and the October 2019 v9.xx User Manual Addendum that includes updated PCA Module syringe compatibility. Verify the installed system software, compatible syringe, and facility configuration before use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Alaris PCA Module v9 Quick Reference Guide
Download PDF
Alaris System User Manual Addendum — October 2019
Download PDF
In stock
$1,225.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Syringe-based patient-controlled analgesia (PCA) module for the Alaris modular infusion system
- Flow rate 0.1–999 mL/h • ±2% rate accuracy excluding syringe variation
- Four operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only • clinician-programmed bolus dose also supported
Refurbished CareFusion Alaris 8120 PCA Module
Refurbished • 1-Year Warranty • Model 8120 syringe-based patient-controlled analgesia module for the Alaris modular system
The CareFusion Alaris 8120 PCA Module is a syringe-based patient-controlled analgesia module designed for facilities that use syringe pumps to deliver medications or fluids. It supports adult, pediatric, and neonatal patients and provides continuous or intermittent delivery through clinically acceptable routes including intravenous, subcutaneous, and epidural administration. The module operates as part of a compatible Alaris System and does not operate as a standalone infusion pump.
What’s Included
- 1× CareFusion Alaris PCA Module, Model 8120
- Dose Request Cord / patient bolus handset included
- Security key(s) for the locking PCA door included
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8120 provides syringe-based PCA functionality within the Alaris modular infusion platform. A locking security door helps control access to the syringe and medication, while the Dose Request Cord allows the patient to request programmed PCA doses when PCA-only or PCA + continuous modes are in use.
The PCA Module supports four manufacturer-defined operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only. A clinician-programmed bolus dose can also be delivered as a separate function after PCA therapy has begun. The PCA Module requires an appropriately configured Alaris System Data Set containing a Drug Library. Guardrails Suite MX then applies facility-defined medication-safety limits and PCA therapy parameters.
- Alaris PCA Module — Model 8120
- Flow rate range: 0.1–999 mL/h, subject to syringe-size restrictions
- Supported flow-rate categories: 20 mL, 30/35 mL, and 50/60 mL; approved syringe models depend on manufacturer and installed PCA Module software
- Rate accuracy: ±2% of full-scale plunger travel, excluding syringe variation
- Three configurable downstream occlusion-pressure settings: Low, Medium, and High
- Optional PCA Pause Protocol can integrate with compatible Alaris SpO2 and/or EtCO2 monitoring modules when configured by the facility
Specifications — CareFusion Alaris PCA Module Model 8120
| Manufacturer | CareFusion |
| Model | 8120 — Alaris PCA Module |
| Type | Syringe-based patient-controlled analgesia (PCA) infusion module |
| System Requirement | Requires a compatible Alaris PC Unit and properly configured Alaris System; does not operate as a standalone pump |
| United Infusion Configuration | Sold for use with the Alaris 8015 PC Unit, sold separately |
| Patient Population | Adult, pediatric, and neonatal patients |
| Intended Delivery | Continuous or intermittent delivery of medications or fluids |
| Administration Routes | Clinically acceptable routes including intravenous (IV), subcutaneous, and epidural administration |
| Operating Modes | PCA Only; Continuous Infusion; PCA + Continuous Infusion; Loading Dose Only |
| Bolus Dose | Clinician-programmed bolus dose available as a separate function during PCA therapy when enabled and permitted by the configured system |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D, exclusive of security door |
| Weight | 5.5 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.10–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| 20 mL Syringe Rate Range | 0.1–500 mL/h |
| 30 / 35 mL Syringe Rate Range | 0.1–650 mL/h |
| 50 / 60 mL Syringe Rate Range | 0.1–999 mL/h |
| Syringe Compatibility | Uses approved single-use disposable luer-lock syringes. Supported flow-rate categories are 20 mL, 30/35 mL, and 50/60 mL. Permitted syringe manufacturer and model combinations depend on PCA Module software version and applicable compatibility documentation. The October 2019 v9.xx addendum confirms compatibility of BD Plastipak 50 mL syringe model 309653, displayed on the Alaris PC Unit as BD Plastipak 50/60 mL. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available syringe-selection list; displayed syringe manufacturer/type and size must be verified before use |
| Rate Accuracy | ±2% of full-scale plunger travel, not including syringe variation |
| Occlusion Alarm Thresholds | Three selectable settings: Low, Medium, and High |
| Occlusion Pressure Set Points | Low: 200 mmHg • Medium: 500 mmHg • High: 800 mmHg |
| Bolus Delivery Rate | Configurable from 75–500 mL/h, limited by syringe size |
| Lockout Interval | 1–99 minutes in 1-minute increments |
| PCA / Loading / Bolus / Maximum Dose Ranges | Configured according to hospital-defined best-practice guidelines through the applicable Drug Library and facility Data Set |
| Patient History | Records and displays up to 24 hours of patient history with selectable 1-, 2-, 4-, 8-, 12-, and 24-hour trend intervals |
| Dose Request Cord | Required for patient-requested PCA dosing in PCA-only and PCA + continuous infusion modes |
| PCA Pause Protocol | Optional hospital-configurable feature; when enabled with compatible SpO2 and/or EtCO2 modules, PCA infusion pauses and alarms when defined monitoring values for low %SpO2 and/or respiratory rate are exceeded and sustained |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part for PCA disposable; Type BF, Defibrillator Proof for Dose Request Cord |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Safety Software | Requires an appropriately configured Alaris System Data Set containing a Drug Library; Guardrails Suite MX applies facility-defined medication-safety limits and PCA therapy parameters |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, the Alaris PCA Module v9 Quick Reference Guide, and the October 2019 v9.xx User Manual Addendum that includes updated PCA Module syringe compatibility. Verify the installed system software, compatible syringe, and facility configuration before use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Alaris PCA Module v9 Quick Reference Guide
Download PDF
Alaris System User Manual Addendum — October 2019
Download PDF
- Syringe-based patient-controlled analgesia (PCA) module for the Alaris modular infusion system
- Flow rate 0.1–999 mL/h • ±2% rate accuracy excluding syringe variation
- Four operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only • clinician-programmed bolus dose also supported
Refurbished CareFusion Alaris 8120 PCA Module
Refurbished • 1-Year Warranty • Model 8120 syringe-based patient-controlled analgesia module for the Alaris modular system
The CareFusion Alaris 8120 PCA Module is a syringe-based patient-controlled analgesia module designed for facilities that use syringe pumps to deliver medications or fluids. It supports adult, pediatric, and neonatal patients and provides continuous or intermittent delivery through clinically acceptable routes including intravenous, subcutaneous, and epidural administration. The module operates as part of a compatible Alaris System and does not operate as a standalone infusion pump.
What’s Included
- 1× CareFusion Alaris PCA Module, Model 8120
- Dose Request Cord / patient bolus handset included
- Security key(s) for the locking PCA door included
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8120 provides syringe-based PCA functionality within the Alaris modular infusion platform. A locking security door helps control access to the syringe and medication, while the Dose Request Cord allows the patient to request programmed PCA doses when PCA-only or PCA + continuous modes are in use.
The PCA Module supports four manufacturer-defined operating modes: PCA only, continuous infusion, PCA + continuous infusion, and loading dose only. A clinician-programmed bolus dose can also be delivered as a separate function after PCA therapy has begun. The PCA Module requires an appropriately configured Alaris System Data Set containing a Drug Library. Guardrails Suite MX then applies facility-defined medication-safety limits and PCA therapy parameters.
- Alaris PCA Module — Model 8120
- Flow rate range: 0.1–999 mL/h, subject to syringe-size restrictions
- Supported flow-rate categories: 20 mL, 30/35 mL, and 50/60 mL; approved syringe models depend on manufacturer and installed PCA Module software
- Rate accuracy: ±2% of full-scale plunger travel, excluding syringe variation
- Three configurable downstream occlusion-pressure settings: Low, Medium, and High
- Optional PCA Pause Protocol can integrate with compatible Alaris SpO2 and/or EtCO2 monitoring modules when configured by the facility
Specifications — CareFusion Alaris PCA Module Model 8120
| Manufacturer | CareFusion |
| Model | 8120 — Alaris PCA Module |
| Type | Syringe-based patient-controlled analgesia (PCA) infusion module |
| System Requirement | Requires a compatible Alaris PC Unit and properly configured Alaris System; does not operate as a standalone pump |
| United Infusion Configuration | Sold for use with the Alaris 8015 PC Unit, sold separately |
| Patient Population | Adult, pediatric, and neonatal patients |
| Intended Delivery | Continuous or intermittent delivery of medications or fluids |
| Administration Routes | Clinically acceptable routes including intravenous (IV), subcutaneous, and epidural administration |
| Operating Modes | PCA Only; Continuous Infusion; PCA + Continuous Infusion; Loading Dose Only |
| Bolus Dose | Clinician-programmed bolus dose available as a separate function during PCA therapy when enabled and permitted by the configured system |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D, exclusive of security door |
| Weight | 5.5 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.10–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| 20 mL Syringe Rate Range | 0.1–500 mL/h |
| 30 / 35 mL Syringe Rate Range | 0.1–650 mL/h |
| 50 / 60 mL Syringe Rate Range | 0.1–999 mL/h |
| Syringe Compatibility | Uses approved single-use disposable luer-lock syringes. Supported flow-rate categories are 20 mL, 30/35 mL, and 50/60 mL. Permitted syringe manufacturer and model combinations depend on PCA Module software version and applicable compatibility documentation. The October 2019 v9.xx addendum confirms compatibility of BD Plastipak 50 mL syringe model 309653, displayed on the Alaris PC Unit as BD Plastipak 50/60 mL. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available syringe-selection list; displayed syringe manufacturer/type and size must be verified before use |
| Rate Accuracy | ±2% of full-scale plunger travel, not including syringe variation |
| Occlusion Alarm Thresholds | Three selectable settings: Low, Medium, and High |
| Occlusion Pressure Set Points | Low: 200 mmHg • Medium: 500 mmHg • High: 800 mmHg |
| Bolus Delivery Rate | Configurable from 75–500 mL/h, limited by syringe size |
| Lockout Interval | 1–99 minutes in 1-minute increments |
| PCA / Loading / Bolus / Maximum Dose Ranges | Configured according to hospital-defined best-practice guidelines through the applicable Drug Library and facility Data Set |
| Patient History | Records and displays up to 24 hours of patient history with selectable 1-, 2-, 4-, 8-, 12-, and 24-hour trend intervals |
| Dose Request Cord | Required for patient-requested PCA dosing in PCA-only and PCA + continuous infusion modes |
| PCA Pause Protocol | Optional hospital-configurable feature; when enabled with compatible SpO2 and/or EtCO2 modules, PCA infusion pauses and alarms when defined monitoring values for low %SpO2 and/or respiratory rate are exceeded and sustained |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part for PCA disposable; Type BF, Defibrillator Proof for Dose Request Cord |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Safety Software | Requires an appropriately configured Alaris System Data Set containing a Drug Library; Guardrails Suite MX applies facility-defined medication-safety limits and PCA therapy parameters |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, the Alaris PCA Module v9 Quick Reference Guide, and the October 2019 v9.xx User Manual Addendum that includes updated PCA Module syringe compatibility. Verify the installed system software, compatible syringe, and facility configuration before use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Alaris PCA Module v9 Quick Reference Guide
Download PDF
Alaris System User Manual Addendum — October 2019
Download PDF
Refurbishing Process
At United Infusion, we follow a comprehensive refurbishing process for infusion pumps to help ensure they operate safely and reliably. This process follows manufacturer guidelines and sanitation standards to meet high quality expectations.
Below are the key steps of our refurbishing process:
2. Disassembly
The pump is carefully disassembled to access internal components, including the motor, gears, tubing pathways, and electronics. All parts are handled with care to avoid added damage.
3. Cleaning & Sanitization
Appropriate disinfectants are used to thoroughly clean all parts and remove residual fluids, blood, or debris. This step follows sanitation standards to help ensure the device is free from contaminants.
4. Component Inspection & Replacement
Individual parts, including the motor, battery, display screen, buttons, and connectors, are inspected for wear, damage, or malfunction. Worn or damaged components are replaced with manufacturer-approved parts.
5. Calibration & Software Update
The pump is adjusted to support accurate fluid delivery rates using standardized testing methods, and calibration is verified against manufacturer specifications. The latest compatible software version is then installed to improve functionality.
6. Testing, Reassembly & Final Check
The pump goes through functional testing, including alarms, flow rate accuracy, occlusion detection, and bolus delivery. It is then reassembled, connections are checked, and a final visual and functional inspection is completed to confirm it meets safety standards and customer requirements.
"We needed our syringe pumps serviced for scheduled maintenance to continue to provide safe care. In the past, we had to send them off with a 6 weeks turn around time. Then we found United Infusion. 30 min down the road, 24 hr turn around and 30 minutes down the road. We are extremely grateful!!!"
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