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.
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
Refurbished Alaris CareFusion EtCO₂ Module 8300
Refurbished • 1-Year Warranty • Model 8300 continuous EtCO₂ respiratory-monitoring module for the Alaris modular system
The Alaris CareFusion EtCO₂ Module, Model 8300 is a sidestream capnography monitoring module designed for continuous, noninvasive measurement of end-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate. It supports intubated and nonintubated adult, pediatric, and neonatal patients and uses Microstream sampling technology with compatible patient sampling lines.
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8300 provides continuous respiratory monitoring using Microstream sidestream capnography. The module measures EtCO₂, FiCO₂, and respiratory rate and provides a real-time capnography waveform, configurable alarm limits, no-breath detection, and respiratory trend information.
The EtCO₂ Module can be used for respiratory monitoring without PCA therapy or integrated with a compatible Alaris PCA Module. When the hospital-configurable PCA Pause Protocol is enabled, respiratory-rate monitoring from the EtCO₂ Module can be used by the Alaris System to pause PCA infusion when configured respiratory limits are exceeded and sustained.
| Manufacturer | CareFusion / BD |
| Model | 8300 — Alaris EtCO₂ Module |
| Type | Continuous sidestream capnography / respiratory-monitoring module |
| Monitoring Technology | Microstream sidestream capnography |
| Monitored Parameters | End-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate (RR) |
| Patient Population | Adult, pediatric, and neonatal patients |
| Patient Applications | Intubated and nonintubated patients using compatible Microstream sampling disposables |
| Monitoring Mode | Continuous |
| PCA Integration | Can integrate with a compatible Alaris PCA Module to support hospital-configured PCA Pause Protocol and shared PCA / EtCO₂ trend information |
| Independent Monitoring | Can be used for EtCO₂ respiratory monitoring without an Alaris PCA Module; verify the applicable Alaris system and software configuration before use |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.5 lb |
| EtCO₂ Measurement Range | 0–99 mmHg at sea level |
| FiCO₂ Measurement Range | 0–99 mmHg at sea level |
| Respiratory Rate Range | 0–150 breaths/min |
| CO₂ Accuracy — 0–38 mmHg | ±2 mmHg under manufacturer-specified test conditions |
| CO₂ Accuracy — 39–99 mmHg | ±(5% of reading + 0.08% for every 1 mmHg above 38 mmHg), subject to manufacturer-specified conditions |
| Respiratory Rate Accuracy | 0–70 breaths/min: ±1 • 71–120 breaths/min: ±2 • 121–150 breaths/min: ±3 |
| Sampling Gas Flow Rate | Nominal 50 mL/min; manufacturer tolerance −7.5 / +15 mL/min |
| EtCO₂ Alarm Limits | Low: 0–98 mmHg • High: 5–99 mmHg |
| FiCO₂ Alarm Limit | High: 2–99 mmHg |
| Respiratory Rate Alarm Limits | Low: 0–149 breaths/min • High: 1–150 breaths/min |
| No-Breath Alarm Limit | 10–60 seconds; configuration and defaults depend on applicable system settings |
| Total System Response Time | Approximately 4.9 seconds typical for the EtCO₂ Module |
| Warm-Up Time | Approximately 30 seconds typical |
| Waveform Sampling | 20 samples/second |
| Internal Power Source | Approximately 5.5 hours operating time when fully charged |
| Compatible Disposables | Use compatible Microstream EtCO₂ sampling lines / disposables specified for the Model 8300 and applicable patient type |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| Defibrillation | Not rated for defibrillation use; manufacturer instructions require disconnection from the patient before defibrillation |
| 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 |
| System / Software | Exact software and Alaris system configuration may vary by refurbished unit; verify installed software and corresponding manufacturer documentation before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, which includes the complete EtCO₂ Module Model 8300 section, plus the CareFusion Alaris EtCO₂ Module v8+ Quick Reference Guide. Verify the installed system software and compatible Microstream sampling disposable before use.
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
Refurbished Alaris CareFusion EtCO₂ Module 8300
Refurbished • 1-Year Warranty • Model 8300 continuous EtCO₂ respiratory-monitoring module for the Alaris modular system
The Alaris CareFusion EtCO₂ Module, Model 8300 is a sidestream capnography monitoring module designed for continuous, noninvasive measurement of end-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate. It supports intubated and nonintubated adult, pediatric, and neonatal patients and uses Microstream sampling technology with compatible patient sampling lines.
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8300 provides continuous respiratory monitoring using Microstream sidestream capnography. The module measures EtCO₂, FiCO₂, and respiratory rate and provides a real-time capnography waveform, configurable alarm limits, no-breath detection, and respiratory trend information.
The EtCO₂ Module can be used for respiratory monitoring without PCA therapy or integrated with a compatible Alaris PCA Module. When the hospital-configurable PCA Pause Protocol is enabled, respiratory-rate monitoring from the EtCO₂ Module can be used by the Alaris System to pause PCA infusion when configured respiratory limits are exceeded and sustained.
| Manufacturer | CareFusion / BD |
| Model | 8300 — Alaris EtCO₂ Module |
| Type | Continuous sidestream capnography / respiratory-monitoring module |
| Monitoring Technology | Microstream sidestream capnography |
| Monitored Parameters | End-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate (RR) |
| Patient Population | Adult, pediatric, and neonatal patients |
| Patient Applications | Intubated and nonintubated patients using compatible Microstream sampling disposables |
| Monitoring Mode | Continuous |
| PCA Integration | Can integrate with a compatible Alaris PCA Module to support hospital-configured PCA Pause Protocol and shared PCA / EtCO₂ trend information |
| Independent Monitoring | Can be used for EtCO₂ respiratory monitoring without an Alaris PCA Module; verify the applicable Alaris system and software configuration before use |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.5 lb |
| EtCO₂ Measurement Range | 0–99 mmHg at sea level |
| FiCO₂ Measurement Range | 0–99 mmHg at sea level |
| Respiratory Rate Range | 0–150 breaths/min |
| CO₂ Accuracy — 0–38 mmHg | ±2 mmHg under manufacturer-specified test conditions |
| CO₂ Accuracy — 39–99 mmHg | ±(5% of reading + 0.08% for every 1 mmHg above 38 mmHg), subject to manufacturer-specified conditions |
| Respiratory Rate Accuracy | 0–70 breaths/min: ±1 • 71–120 breaths/min: ±2 • 121–150 breaths/min: ±3 |
| Sampling Gas Flow Rate | Nominal 50 mL/min; manufacturer tolerance −7.5 / +15 mL/min |
| EtCO₂ Alarm Limits | Low: 0–98 mmHg • High: 5–99 mmHg |
| FiCO₂ Alarm Limit | High: 2–99 mmHg |
| Respiratory Rate Alarm Limits | Low: 0–149 breaths/min • High: 1–150 breaths/min |
| No-Breath Alarm Limit | 10–60 seconds; configuration and defaults depend on applicable system settings |
| Total System Response Time | Approximately 4.9 seconds typical for the EtCO₂ Module |
| Warm-Up Time | Approximately 30 seconds typical |
| Waveform Sampling | 20 samples/second |
| Internal Power Source | Approximately 5.5 hours operating time when fully charged |
| Compatible Disposables | Use compatible Microstream EtCO₂ sampling lines / disposables specified for the Model 8300 and applicable patient type |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| Defibrillation | Not rated for defibrillation use; manufacturer instructions require disconnection from the patient before defibrillation |
| 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 |
| System / Software | Exact software and Alaris system configuration may vary by refurbished unit; verify installed software and corresponding manufacturer documentation before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, which includes the complete EtCO₂ Module Model 8300 section, plus the CareFusion Alaris EtCO₂ Module v8+ Quick Reference Guide. Verify the installed system software and compatible Microstream sampling disposable before use.
Refurbished Alaris CareFusion EtCO₂ Module 8300
Refurbished • 1-Year Warranty • Model 8300 continuous EtCO₂ respiratory-monitoring module for the Alaris modular system
The Alaris CareFusion EtCO₂ Module, Model 8300 is a sidestream capnography monitoring module designed for continuous, noninvasive measurement of end-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate. It supports intubated and nonintubated adult, pediatric, and neonatal patients and uses Microstream sampling technology with compatible patient sampling lines.
Fully refurbished and backed by a 1-year United Infusion warranty, the Alaris 8300 provides continuous respiratory monitoring using Microstream sidestream capnography. The module measures EtCO₂, FiCO₂, and respiratory rate and provides a real-time capnography waveform, configurable alarm limits, no-breath detection, and respiratory trend information.
The EtCO₂ Module can be used for respiratory monitoring without PCA therapy or integrated with a compatible Alaris PCA Module. When the hospital-configurable PCA Pause Protocol is enabled, respiratory-rate monitoring from the EtCO₂ Module can be used by the Alaris System to pause PCA infusion when configured respiratory limits are exceeded and sustained.
| Manufacturer | CareFusion / BD |
| Model | 8300 — Alaris EtCO₂ Module |
| Type | Continuous sidestream capnography / respiratory-monitoring module |
| Monitoring Technology | Microstream sidestream capnography |
| Monitored Parameters | End-tidal carbon dioxide (EtCO₂), fractional inspired carbon dioxide (FiCO₂), and respiratory rate (RR) |
| Patient Population | Adult, pediatric, and neonatal patients |
| Patient Applications | Intubated and nonintubated patients using compatible Microstream sampling disposables |
| Monitoring Mode | Continuous |
| PCA Integration | Can integrate with a compatible Alaris PCA Module to support hospital-configured PCA Pause Protocol and shared PCA / EtCO₂ trend information |
| Independent Monitoring | Can be used for EtCO₂ respiratory monitoring without an Alaris PCA Module; verify the applicable Alaris system and software configuration before use |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.5 lb |
| EtCO₂ Measurement Range | 0–99 mmHg at sea level |
| FiCO₂ Measurement Range | 0–99 mmHg at sea level |
| Respiratory Rate Range | 0–150 breaths/min |
| CO₂ Accuracy — 0–38 mmHg | ±2 mmHg under manufacturer-specified test conditions |
| CO₂ Accuracy — 39–99 mmHg | ±(5% of reading + 0.08% for every 1 mmHg above 38 mmHg), subject to manufacturer-specified conditions |
| Respiratory Rate Accuracy | 0–70 breaths/min: ±1 • 71–120 breaths/min: ±2 • 121–150 breaths/min: ±3 |
| Sampling Gas Flow Rate | Nominal 50 mL/min; manufacturer tolerance −7.5 / +15 mL/min |
| EtCO₂ Alarm Limits | Low: 0–98 mmHg • High: 5–99 mmHg |
| FiCO₂ Alarm Limit | High: 2–99 mmHg |
| Respiratory Rate Alarm Limits | Low: 0–149 breaths/min • High: 1–150 breaths/min |
| No-Breath Alarm Limit | 10–60 seconds; configuration and defaults depend on applicable system settings |
| Total System Response Time | Approximately 4.9 seconds typical for the EtCO₂ Module |
| Warm-Up Time | Approximately 30 seconds typical |
| Waveform Sampling | 20 samples/second |
| Internal Power Source | Approximately 5.5 hours operating time when fully charged |
| Compatible Disposables | Use compatible Microstream EtCO₂ sampling lines / disposables specified for the Model 8300 and applicable patient type |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type BF patient-applied part |
| Defibrillation | Not rated for defibrillation use; manufacturer instructions require disconnection from the patient before defibrillation |
| 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 |
| System / Software | Exact software and Alaris system configuration may vary by refurbished unit; verify installed software and corresponding manufacturer documentation before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Download the CareFusion Alaris System User Manual for PC Unit Model 8015, Software Version 9.33, which includes the complete EtCO₂ Module Model 8300 section, plus the CareFusion Alaris EtCO₂ Module v8+ Quick Reference Guide. Verify the installed system software and compatible Microstream sampling disposable before use.
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:
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.
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.
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.
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.
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.
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.
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