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 Alaris 8200 SpO2 Infusion IV Pump
In stock
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Masimo SET pulse-oximetry monitoring module for the Alaris modular system
- SpO2 measurement range 1–100% • pulse rate 25–240 bpm • perfusion range 0.02–20%
- Continuous, noninvasive monitoring for adult, pediatric, and neonatal patients • requires a compatible Alaris PC Unit
Refurbished CareFusion Alaris 8220 SpO2 Module
Refurbished • 1-Year Warranty • Model 8220 Masimo SET pulse-oximetry monitoring module for the Alaris modular system
The CareFusion Alaris 8220 SpO2 Module provides continuous, noninvasive monitoring of functional arterial oxygen saturation (SpO2) and pulse rate within a compatible Alaris modular system. Model 8220 uses Masimo SET pulse-oximetry technology and is intended for adult, pediatric, and neonatal patients, including patients who are well or poorly perfused. It is also indicated for monitoring during motion and no-motion conditions. The module does not operate as a standalone monitor and requires a compatible Alaris PC Unit.
What’s Included
- 1× CareFusion Alaris SpO2 Module, Model 8220
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8220 adds Masimo SET pulse-oximetry monitoring to a compatible Alaris System. The module measures and displays SpO2 and pulse rate while providing configurable alarm limits, trend information, a plethysmographic waveform, Signal I.Q., and perfusion-index information through the Alaris system interface.
Model 8220 uses approved Masimo sensors and patient cables. Saturation averaging can be configured from 2 to 16 seconds using the supported selectable values, and Normal or Maximum sensitivity modes are available. Maximum sensitivity is intended to improve low-perfusion performance.
- Alaris SpO2 Module — Model 8220 with Masimo SET technology
- Continuous SpO2 and pulse-rate monitoring
- SpO2 measurement range: 1–100%
- Pulse-rate measurement range: 25–240 bpm
- Perfusion measurement range: 0.02–20%
- Designed for adult, pediatric, and neonatal patients during motion and no-motion conditions
Specifications — CareFusion Alaris SpO2 Module Model 8220
| Manufacturer | CareFusion / ALARIS Medical Systems |
| Model | 8220 — Alaris SpO2 Module |
| Type | Continuous pulse-oximetry monitoring module |
| Monitoring Technology | Masimo SET pulse oximetry |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone monitoring device |
| United Infusion Configuration | Sold for use with compatible Alaris / CareFusion system configurations; verify PC Unit and installed software before use |
| Patient Population | Adult, pediatric, and neonatal patients |
| Clinical Use | Continuous, noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate |
| Patient Conditions | Indicated for well- or poorly-perfused patients and for motion and no-motion conditions |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2 lb (0.91 kg) |
| Mode of Operation | Continuous |
| SpO2 Measurement Range | 1–100% |
| Pulse Rate Measurement Range | 25–240 bpm |
| Perfusion Measurement Range | 0.02–20% |
| Display Update Period | Approximately 1 second |
| SpO2 Alarm Limit Range | Low: 20–99% • High: 21–100% or Off |
| Pulse Rate Alarm Limit Range | Low: 30–239 bpm • High: 31–240 bpm |
| Saturation Averaging Time | Selectable 2, 4, 8, 10, 12, 14, or 16 seconds; 8 seconds is the referenced factory default |
| Sensitivity Modes | Normal or Maximum; Maximum is intended for improved low-perfusion performance |
| Display Features | SpO2, pulse rate, plethysmographic waveform, Signal I.Q., perfusion index, alarm limits, and trend data |
| Trend Data | Displays SpO2 and pulse-rate trends through the connected Alaris system |
| Compatible Sensors / Cables | Use approved Masimo sensors and patient cables appropriate for the Model 8220 configuration and installed software |
| Fluid Ingress Protection | IPX1 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| 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 | 5–85% noncondensing in the Model 8220 Series Version 7 Directions for Use; 5–90% noncondensing in the Alaris System v9.33 User Manual for legacy SpO2 users upgraded to v9.33. Verify installed software and applicable documentation. |
| Software / Manual Reference | The Alaris System v9.33 SpO2 section applies specifically to legacy SpO2 users upgraded with v9.33 software. Verify the installed software version and use the corresponding manufacturer documentation before clinical use. |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Model 8220 Series Masimo SpO2 Directions for Use and the CareFusion Alaris System User Manual covering SpO2 Module Models 8210 and 8220. The v9.33 SpO2 section applies to legacy SpO2 users upgraded with v9.33 software. Verify the installed system software and compatible Masimo sensors and patient cables before use.
Alaris Medley SpO2 Module 8220 Series Directions for Use
Download PDF
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
In stock
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Masimo SET pulse-oximetry monitoring module for the Alaris modular system
- SpO2 measurement range 1–100% • pulse rate 25–240 bpm • perfusion range 0.02–20%
- Continuous, noninvasive monitoring for adult, pediatric, and neonatal patients • requires a compatible Alaris PC Unit
Refurbished CareFusion Alaris 8220 SpO2 Module
Refurbished • 1-Year Warranty • Model 8220 Masimo SET pulse-oximetry monitoring module for the Alaris modular system
The CareFusion Alaris 8220 SpO2 Module provides continuous, noninvasive monitoring of functional arterial oxygen saturation (SpO2) and pulse rate within a compatible Alaris modular system. Model 8220 uses Masimo SET pulse-oximetry technology and is intended for adult, pediatric, and neonatal patients, including patients who are well or poorly perfused. It is also indicated for monitoring during motion and no-motion conditions. The module does not operate as a standalone monitor and requires a compatible Alaris PC Unit.
What’s Included
- 1× CareFusion Alaris SpO2 Module, Model 8220
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8220 adds Masimo SET pulse-oximetry monitoring to a compatible Alaris System. The module measures and displays SpO2 and pulse rate while providing configurable alarm limits, trend information, a plethysmographic waveform, Signal I.Q., and perfusion-index information through the Alaris system interface.
Model 8220 uses approved Masimo sensors and patient cables. Saturation averaging can be configured from 2 to 16 seconds using the supported selectable values, and Normal or Maximum sensitivity modes are available. Maximum sensitivity is intended to improve low-perfusion performance.
- Alaris SpO2 Module — Model 8220 with Masimo SET technology
- Continuous SpO2 and pulse-rate monitoring
- SpO2 measurement range: 1–100%
- Pulse-rate measurement range: 25–240 bpm
- Perfusion measurement range: 0.02–20%
- Designed for adult, pediatric, and neonatal patients during motion and no-motion conditions
Specifications — CareFusion Alaris SpO2 Module Model 8220
| Manufacturer | CareFusion / ALARIS Medical Systems |
| Model | 8220 — Alaris SpO2 Module |
| Type | Continuous pulse-oximetry monitoring module |
| Monitoring Technology | Masimo SET pulse oximetry |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone monitoring device |
| United Infusion Configuration | Sold for use with compatible Alaris / CareFusion system configurations; verify PC Unit and installed software before use |
| Patient Population | Adult, pediatric, and neonatal patients |
| Clinical Use | Continuous, noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate |
| Patient Conditions | Indicated for well- or poorly-perfused patients and for motion and no-motion conditions |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2 lb (0.91 kg) |
| Mode of Operation | Continuous |
| SpO2 Measurement Range | 1–100% |
| Pulse Rate Measurement Range | 25–240 bpm |
| Perfusion Measurement Range | 0.02–20% |
| Display Update Period | Approximately 1 second |
| SpO2 Alarm Limit Range | Low: 20–99% • High: 21–100% or Off |
| Pulse Rate Alarm Limit Range | Low: 30–239 bpm • High: 31–240 bpm |
| Saturation Averaging Time | Selectable 2, 4, 8, 10, 12, 14, or 16 seconds; 8 seconds is the referenced factory default |
| Sensitivity Modes | Normal or Maximum; Maximum is intended for improved low-perfusion performance |
| Display Features | SpO2, pulse rate, plethysmographic waveform, Signal I.Q., perfusion index, alarm limits, and trend data |
| Trend Data | Displays SpO2 and pulse-rate trends through the connected Alaris system |
| Compatible Sensors / Cables | Use approved Masimo sensors and patient cables appropriate for the Model 8220 configuration and installed software |
| Fluid Ingress Protection | IPX1 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| 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 | 5–85% noncondensing in the Model 8220 Series Version 7 Directions for Use; 5–90% noncondensing in the Alaris System v9.33 User Manual for legacy SpO2 users upgraded to v9.33. Verify installed software and applicable documentation. |
| Software / Manual Reference | The Alaris System v9.33 SpO2 section applies specifically to legacy SpO2 users upgraded with v9.33 software. Verify the installed software version and use the corresponding manufacturer documentation before clinical use. |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Model 8220 Series Masimo SpO2 Directions for Use and the CareFusion Alaris System User Manual covering SpO2 Module Models 8210 and 8220. The v9.33 SpO2 section applies to legacy SpO2 users upgraded with v9.33 software. Verify the installed system software and compatible Masimo sensors and patient cables before use.
Alaris Medley SpO2 Module 8220 Series Directions for Use
Download PDF
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
- Masimo SET pulse-oximetry monitoring module for the Alaris modular system
- SpO2 measurement range 1–100% • pulse rate 25–240 bpm • perfusion range 0.02–20%
- Continuous, noninvasive monitoring for adult, pediatric, and neonatal patients • requires a compatible Alaris PC Unit
Refurbished CareFusion Alaris 8220 SpO2 Module
Refurbished • 1-Year Warranty • Model 8220 Masimo SET pulse-oximetry monitoring module for the Alaris modular system
The CareFusion Alaris 8220 SpO2 Module provides continuous, noninvasive monitoring of functional arterial oxygen saturation (SpO2) and pulse rate within a compatible Alaris modular system. Model 8220 uses Masimo SET pulse-oximetry technology and is intended for adult, pediatric, and neonatal patients, including patients who are well or poorly perfused. It is also indicated for monitoring during motion and no-motion conditions. The module does not operate as a standalone monitor and requires a compatible Alaris PC Unit.
What’s Included
- 1× CareFusion Alaris SpO2 Module, Model 8220
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8220 adds Masimo SET pulse-oximetry monitoring to a compatible Alaris System. The module measures and displays SpO2 and pulse rate while providing configurable alarm limits, trend information, a plethysmographic waveform, Signal I.Q., and perfusion-index information through the Alaris system interface.
Model 8220 uses approved Masimo sensors and patient cables. Saturation averaging can be configured from 2 to 16 seconds using the supported selectable values, and Normal or Maximum sensitivity modes are available. Maximum sensitivity is intended to improve low-perfusion performance.
- Alaris SpO2 Module — Model 8220 with Masimo SET technology
- Continuous SpO2 and pulse-rate monitoring
- SpO2 measurement range: 1–100%
- Pulse-rate measurement range: 25–240 bpm
- Perfusion measurement range: 0.02–20%
- Designed for adult, pediatric, and neonatal patients during motion and no-motion conditions
Specifications — CareFusion Alaris SpO2 Module Model 8220
| Manufacturer | CareFusion / ALARIS Medical Systems |
| Model | 8220 — Alaris SpO2 Module |
| Type | Continuous pulse-oximetry monitoring module |
| Monitoring Technology | Masimo SET pulse oximetry |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone monitoring device |
| United Infusion Configuration | Sold for use with compatible Alaris / CareFusion system configurations; verify PC Unit and installed software before use |
| Patient Population | Adult, pediatric, and neonatal patients |
| Clinical Use | Continuous, noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate |
| Patient Conditions | Indicated for well- or poorly-perfused patients and for motion and no-motion conditions |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2 lb (0.91 kg) |
| Mode of Operation | Continuous |
| SpO2 Measurement Range | 1–100% |
| Pulse Rate Measurement Range | 25–240 bpm |
| Perfusion Measurement Range | 0.02–20% |
| Display Update Period | Approximately 1 second |
| SpO2 Alarm Limit Range | Low: 20–99% • High: 21–100% or Off |
| Pulse Rate Alarm Limit Range | Low: 30–239 bpm • High: 31–240 bpm |
| Saturation Averaging Time | Selectable 2, 4, 8, 10, 12, 14, or 16 seconds; 8 seconds is the referenced factory default |
| Sensitivity Modes | Normal or Maximum; Maximum is intended for improved low-perfusion performance |
| Display Features | SpO2, pulse rate, plethysmographic waveform, Signal I.Q., perfusion index, alarm limits, and trend data |
| Trend Data | Displays SpO2 and pulse-rate trends through the connected Alaris system |
| Compatible Sensors / Cables | Use approved Masimo sensors and patient cables appropriate for the Model 8220 configuration and installed software |
| Fluid Ingress Protection | IPX1 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| 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 | 5–85% noncondensing in the Model 8220 Series Version 7 Directions for Use; 5–90% noncondensing in the Alaris System v9.33 User Manual for legacy SpO2 users upgraded to v9.33. Verify installed software and applicable documentation. |
| Software / Manual Reference | The Alaris System v9.33 SpO2 section applies specifically to legacy SpO2 users upgraded with v9.33 software. Verify the installed software version and use the corresponding manufacturer documentation before clinical use. |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Model 8220 Series Masimo SpO2 Directions for Use and the CareFusion Alaris System User Manual covering SpO2 Module Models 8210 and 8220. The v9.33 SpO2 section applies to legacy SpO2 users upgraded with v9.33 software. Verify the installed system software and compatible Masimo sensors and patient cables before use.
Alaris Medley SpO2 Module 8220 Series Directions for Use
Download PDF
Alaris System User Manual — PC Unit Model 8015, Software v9.33
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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