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 Baxter Infus O.R. Infusion Pump
In stock
$3,899.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- 0–600 mL/h flow range depending on SMART LABEL • ±3% infusion linear-rate accuracy
- Compatible with specified B-D® or Monoject® 20 cc and 60 cc plastic syringes
- Magnetically coded SMART LABEL programming • label-specific infusion modes and delivery functions
Refurbished Baxter Infus O.R. Infusion Pump
Refurbished • 1-Year Warranty • Battery-powered syringe infusion pump with SMART LABEL programming
The Baxter InfusO.R. Pump is a battery-powered syringe infusion device designed to assist in the administration of intravenous agents during anesthetic procedures. Its magnetically coded SMART LABEL System configures the pump for drug-specific concentration, syringe size, dosing units, infusion settings, and applicable bolus or low-infusion-rate functions.
What’s Included
- 1× Refurbished Baxter Infus O.R. Infusion Pump
Product Description
Refurbished and backed by a 1-year United Infusion warranty, the InfusO.R. uses magnetically coded SMART LABELS together with front-panel rotary controls to support syringe-based infusion during anesthetic procedures. A compatible SMART LABEL must be attached for pump operation to commence. Depending on the selected label, the controls provide appropriate infusion-rate, body-weight, bolus, or low-infusion-rate functions for the identified drug and syringe configuration.
- Flow rates from 0–600 mL/h, depending on the installed SMART LABEL
- Infusion linear-rate accuracy of ±3%
- Bolus linear-displacement accuracy of ±3%
- Supports specified B-D® and Monoject® 20 cc and 60 cc plastic disposable syringes
- A compatible SMART LABEL must be attached to the pump for operation to commence
- SMART LABELS define drug-specific concentration, syringe size, dosing units, rates, and applicable delivery functions
- Front-panel rotary controls allow permitted infusion settings to be adjusted during operation
- Intermittent pulsed infusion profile with continuous bolus delivery when bolus operation is enabled by the applicable SMART LABEL
- Digital display shows total drug volume delivered since the pump was last turned on; switching the Function control to OFF clears the display and internal memory
- Monitors conditions including occlusion, end of syringe, low battery, missing SMART LABEL, improper switch position, and internal fault
- Manufacturer-published compatible anesthesia sets include Baxter 2C9215, 2C9216, and 2C9218
Specifications — Baxter InfusO.R.
| Manufacturer | Baxter Healthcare Corporation |
| Model | InfusO.R. Syringe Infusion Pump |
| Baxter Catalog Identifiers | Baxter’s current U.S. catalog lists 2L3100 / 6461500 for the standard catalog entry and 2L3100R / 6461500R for a separate Baxter-refurbished catalog entry. Verify the exact manufacturer identifier on the physical device label. |
| United Infusion SKU | 2L3100R1 |
| Type | Battery-powered syringe infusion pump |
| Programming System | Magnetically coded, drug-specific SMART LABEL System. Available dosing units, concentrations, syringe requirements, rates, and delivery functions depend on the applicable SMART LABEL. |
| SMART LABEL Requirement | A compatible SMART LABEL must be attached to the face of the pump for operation to commence. SMART LABEL inclusion with the United Infusion unit should be confirmed separately. |
| Flow Rate | 0–600 mL/h, depending on SMART LABEL |
| Infusion Accuracy | ±3% linear rate |
| Bolus Accuracy | ±3% linear displacement |
| Flow Profile | Infusion: pulsed intermittently. Bolus: continuous when bolus delivery is enabled by the applicable SMART LABEL. |
| Volume Display / Memory | During normal infusion, the digital display shows the total amount of drug delivered in mL since the pump was last turned on. Moving the Function control to OFF clears the display and all internal memory. |
| Syringe Compatibility | Specified B-D® or Monoject® 20 cc and 60 cc plastic disposable syringes. Use the syringe manufacturer and size identified by the applicable SMART LABEL. |
| Manufacturer-Published Compatible Anesthesia Sets | Baxter 2C9215 — anti-siphon anesthesia set with blue stripe; Baxter 2C9216 — anesthesia set with green stripe; Baxter 2C9218 — universal anesthesia set with yellow stripe for higher-viscosity drugs. Verify the specific set and configuration required for the intended application. |
| Occlusion Force | 8 ± 1 lb |
| Maximum Occlusion Pressure | 11 psi with a 60 cc syringe; 20 psi with a 20 cc syringe |
| Occlusion Detection | 120 seconds at 36 mL/h; detection time is inversely related to flow rate. Published test condition uses a microbore anesthesia set and 60 cc syringe. |
| Volume Stored on Occlusion | Approximately 1.1 mL under the manufacturer’s stated microbore anesthesia-set / 60 cc syringe test condition |
| Back Pressure Effect on Accuracy | None to occlusion pressure |
| Dimensions | 9.2″ × 4.5″ × 2.0″ |
| Weight | 2 lb (approximately 1 kg) with batteries |
| Power | Four C-size alkaline cells, ANSI/NEDA 14A |
| Operating Voltage | 5–7 V |
| Published Battery Life | 150 hours under typical use; 4 hours at the low-battery condition under typical use. Battery life is affected by factors including bolus duration, backpressure, and audible alarm duration. |
| Operating Environment | Designed for operating-room delivery of parenteral fluids under constant surveillance by individuals trained in administration of these agents. Baxter does not recommend use when surveillance is not continual. |
| Electric / Magnetic Field & Radiation Limitation | Manufacturer documentation does not recommend use near electric fields, magnetic fields, or radiation, including electrosurgical units, MRI equipment, and X-ray equipment, because device malfunction may result. |
| Fluid Protection | Drip-proof equipment that prevents entry of falling liquids; not watertight. Do not immerse in liquid or expose the pump to possible splash or sprayed liquids. |
| Electrical Classification | Type BF equipment with internal battery power source |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter InfusO.R. Pump User’s Manual.
The linked PDF is a Baxter Healthcare Corporation manufacturer manual, document 5371151, with cover marking 05/02 and an issue date of December 1998. Baxter currently maintains U.S. catalog records for standard product code 2L3100 and separate Baxter-refurbished product code 2L3100R. Verify the exact pump identifier, SMART LABEL, syringe, and administration-set configuration before use.
Baxter InfusO.R. Pump User’s Manual
Download PDF
In stock
$3,899.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- 0–600 mL/h flow range depending on SMART LABEL • ±3% infusion linear-rate accuracy
- Compatible with specified B-D® or Monoject® 20 cc and 60 cc plastic syringes
- Magnetically coded SMART LABEL programming • label-specific infusion modes and delivery functions
Refurbished Baxter Infus O.R. Infusion Pump
Refurbished • 1-Year Warranty • Battery-powered syringe infusion pump with SMART LABEL programming
The Baxter InfusO.R. Pump is a battery-powered syringe infusion device designed to assist in the administration of intravenous agents during anesthetic procedures. Its magnetically coded SMART LABEL System configures the pump for drug-specific concentration, syringe size, dosing units, infusion settings, and applicable bolus or low-infusion-rate functions.
What’s Included
- 1× Refurbished Baxter Infus O.R. Infusion Pump
Product Description
Refurbished and backed by a 1-year United Infusion warranty, the InfusO.R. uses magnetically coded SMART LABELS together with front-panel rotary controls to support syringe-based infusion during anesthetic procedures. A compatible SMART LABEL must be attached for pump operation to commence. Depending on the selected label, the controls provide appropriate infusion-rate, body-weight, bolus, or low-infusion-rate functions for the identified drug and syringe configuration.
- Flow rates from 0–600 mL/h, depending on the installed SMART LABEL
- Infusion linear-rate accuracy of ±3%
- Bolus linear-displacement accuracy of ±3%
- Supports specified B-D® and Monoject® 20 cc and 60 cc plastic disposable syringes
- A compatible SMART LABEL must be attached to the pump for operation to commence
- SMART LABELS define drug-specific concentration, syringe size, dosing units, rates, and applicable delivery functions
- Front-panel rotary controls allow permitted infusion settings to be adjusted during operation
- Intermittent pulsed infusion profile with continuous bolus delivery when bolus operation is enabled by the applicable SMART LABEL
- Digital display shows total drug volume delivered since the pump was last turned on; switching the Function control to OFF clears the display and internal memory
- Monitors conditions including occlusion, end of syringe, low battery, missing SMART LABEL, improper switch position, and internal fault
- Manufacturer-published compatible anesthesia sets include Baxter 2C9215, 2C9216, and 2C9218
Specifications — Baxter InfusO.R.
| Manufacturer | Baxter Healthcare Corporation |
| Model | InfusO.R. Syringe Infusion Pump |
| Baxter Catalog Identifiers | Baxter’s current U.S. catalog lists 2L3100 / 6461500 for the standard catalog entry and 2L3100R / 6461500R for a separate Baxter-refurbished catalog entry. Verify the exact manufacturer identifier on the physical device label. |
| United Infusion SKU | 2L3100R1 |
| Type | Battery-powered syringe infusion pump |
| Programming System | Magnetically coded, drug-specific SMART LABEL System. Available dosing units, concentrations, syringe requirements, rates, and delivery functions depend on the applicable SMART LABEL. |
| SMART LABEL Requirement | A compatible SMART LABEL must be attached to the face of the pump for operation to commence. SMART LABEL inclusion with the United Infusion unit should be confirmed separately. |
| Flow Rate | 0–600 mL/h, depending on SMART LABEL |
| Infusion Accuracy | ±3% linear rate |
| Bolus Accuracy | ±3% linear displacement |
| Flow Profile | Infusion: pulsed intermittently. Bolus: continuous when bolus delivery is enabled by the applicable SMART LABEL. |
| Volume Display / Memory | During normal infusion, the digital display shows the total amount of drug delivered in mL since the pump was last turned on. Moving the Function control to OFF clears the display and all internal memory. |
| Syringe Compatibility | Specified B-D® or Monoject® 20 cc and 60 cc plastic disposable syringes. Use the syringe manufacturer and size identified by the applicable SMART LABEL. |
| Manufacturer-Published Compatible Anesthesia Sets | Baxter 2C9215 — anti-siphon anesthesia set with blue stripe; Baxter 2C9216 — anesthesia set with green stripe; Baxter 2C9218 — universal anesthesia set with yellow stripe for higher-viscosity drugs. Verify the specific set and configuration required for the intended application. |
| Occlusion Force | 8 ± 1 lb |
| Maximum Occlusion Pressure | 11 psi with a 60 cc syringe; 20 psi with a 20 cc syringe |
| Occlusion Detection | 120 seconds at 36 mL/h; detection time is inversely related to flow rate. Published test condition uses a microbore anesthesia set and 60 cc syringe. |
| Volume Stored on Occlusion | Approximately 1.1 mL under the manufacturer’s stated microbore anesthesia-set / 60 cc syringe test condition |
| Back Pressure Effect on Accuracy | None to occlusion pressure |
| Dimensions | 9.2″ × 4.5″ × 2.0″ |
| Weight | 2 lb (approximately 1 kg) with batteries |
| Power | Four C-size alkaline cells, ANSI/NEDA 14A |
| Operating Voltage | 5–7 V |
| Published Battery Life | 150 hours under typical use; 4 hours at the low-battery condition under typical use. Battery life is affected by factors including bolus duration, backpressure, and audible alarm duration. |
| Operating Environment | Designed for operating-room delivery of parenteral fluids under constant surveillance by individuals trained in administration of these agents. Baxter does not recommend use when surveillance is not continual. |
| Electric / Magnetic Field & Radiation Limitation | Manufacturer documentation does not recommend use near electric fields, magnetic fields, or radiation, including electrosurgical units, MRI equipment, and X-ray equipment, because device malfunction may result. |
| Fluid Protection | Drip-proof equipment that prevents entry of falling liquids; not watertight. Do not immerse in liquid or expose the pump to possible splash or sprayed liquids. |
| Electrical Classification | Type BF equipment with internal battery power source |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter InfusO.R. Pump User’s Manual.
The linked PDF is a Baxter Healthcare Corporation manufacturer manual, document 5371151, with cover marking 05/02 and an issue date of December 1998. Baxter currently maintains U.S. catalog records for standard product code 2L3100 and separate Baxter-refurbished product code 2L3100R. Verify the exact pump identifier, SMART LABEL, syringe, and administration-set configuration before use.
Baxter InfusO.R. Pump User’s Manual
Download PDF
- 0–600 mL/h flow range depending on SMART LABEL • ±3% infusion linear-rate accuracy
- Compatible with specified B-D® or Monoject® 20 cc and 60 cc plastic syringes
- Magnetically coded SMART LABEL programming • label-specific infusion modes and delivery functions
Refurbished Baxter Infus O.R. Infusion Pump
Refurbished • 1-Year Warranty • Battery-powered syringe infusion pump with SMART LABEL programming
The Baxter InfusO.R. Pump is a battery-powered syringe infusion device designed to assist in the administration of intravenous agents during anesthetic procedures. Its magnetically coded SMART LABEL System configures the pump for drug-specific concentration, syringe size, dosing units, infusion settings, and applicable bolus or low-infusion-rate functions.
What’s Included
- 1× Refurbished Baxter Infus O.R. Infusion Pump
Product Description
Refurbished and backed by a 1-year United Infusion warranty, the InfusO.R. uses magnetically coded SMART LABELS together with front-panel rotary controls to support syringe-based infusion during anesthetic procedures. A compatible SMART LABEL must be attached for pump operation to commence. Depending on the selected label, the controls provide appropriate infusion-rate, body-weight, bolus, or low-infusion-rate functions for the identified drug and syringe configuration.
- Flow rates from 0–600 mL/h, depending on the installed SMART LABEL
- Infusion linear-rate accuracy of ±3%
- Bolus linear-displacement accuracy of ±3%
- Supports specified B-D® and Monoject® 20 cc and 60 cc plastic disposable syringes
- A compatible SMART LABEL must be attached to the pump for operation to commence
- SMART LABELS define drug-specific concentration, syringe size, dosing units, rates, and applicable delivery functions
- Front-panel rotary controls allow permitted infusion settings to be adjusted during operation
- Intermittent pulsed infusion profile with continuous bolus delivery when bolus operation is enabled by the applicable SMART LABEL
- Digital display shows total drug volume delivered since the pump was last turned on; switching the Function control to OFF clears the display and internal memory
- Monitors conditions including occlusion, end of syringe, low battery, missing SMART LABEL, improper switch position, and internal fault
- Manufacturer-published compatible anesthesia sets include Baxter 2C9215, 2C9216, and 2C9218
Specifications — Baxter InfusO.R.
| Manufacturer | Baxter Healthcare Corporation |
| Model | InfusO.R. Syringe Infusion Pump |
| Baxter Catalog Identifiers | Baxter’s current U.S. catalog lists 2L3100 / 6461500 for the standard catalog entry and 2L3100R / 6461500R for a separate Baxter-refurbished catalog entry. Verify the exact manufacturer identifier on the physical device label. |
| United Infusion SKU | 2L3100R1 |
| Type | Battery-powered syringe infusion pump |
| Programming System | Magnetically coded, drug-specific SMART LABEL System. Available dosing units, concentrations, syringe requirements, rates, and delivery functions depend on the applicable SMART LABEL. |
| SMART LABEL Requirement | A compatible SMART LABEL must be attached to the face of the pump for operation to commence. SMART LABEL inclusion with the United Infusion unit should be confirmed separately. |
| Flow Rate | 0–600 mL/h, depending on SMART LABEL |
| Infusion Accuracy | ±3% linear rate |
| Bolus Accuracy | ±3% linear displacement |
| Flow Profile | Infusion: pulsed intermittently. Bolus: continuous when bolus delivery is enabled by the applicable SMART LABEL. |
| Volume Display / Memory | During normal infusion, the digital display shows the total amount of drug delivered in mL since the pump was last turned on. Moving the Function control to OFF clears the display and all internal memory. |
| Syringe Compatibility | Specified B-D® or Monoject® 20 cc and 60 cc plastic disposable syringes. Use the syringe manufacturer and size identified by the applicable SMART LABEL. |
| Manufacturer-Published Compatible Anesthesia Sets | Baxter 2C9215 — anti-siphon anesthesia set with blue stripe; Baxter 2C9216 — anesthesia set with green stripe; Baxter 2C9218 — universal anesthesia set with yellow stripe for higher-viscosity drugs. Verify the specific set and configuration required for the intended application. |
| Occlusion Force | 8 ± 1 lb |
| Maximum Occlusion Pressure | 11 psi with a 60 cc syringe; 20 psi with a 20 cc syringe |
| Occlusion Detection | 120 seconds at 36 mL/h; detection time is inversely related to flow rate. Published test condition uses a microbore anesthesia set and 60 cc syringe. |
| Volume Stored on Occlusion | Approximately 1.1 mL under the manufacturer’s stated microbore anesthesia-set / 60 cc syringe test condition |
| Back Pressure Effect on Accuracy | None to occlusion pressure |
| Dimensions | 9.2″ × 4.5″ × 2.0″ |
| Weight | 2 lb (approximately 1 kg) with batteries |
| Power | Four C-size alkaline cells, ANSI/NEDA 14A |
| Operating Voltage | 5–7 V |
| Published Battery Life | 150 hours under typical use; 4 hours at the low-battery condition under typical use. Battery life is affected by factors including bolus duration, backpressure, and audible alarm duration. |
| Operating Environment | Designed for operating-room delivery of parenteral fluids under constant surveillance by individuals trained in administration of these agents. Baxter does not recommend use when surveillance is not continual. |
| Electric / Magnetic Field & Radiation Limitation | Manufacturer documentation does not recommend use near electric fields, magnetic fields, or radiation, including electrosurgical units, MRI equipment, and X-ray equipment, because device malfunction may result. |
| Fluid Protection | Drip-proof equipment that prevents entry of falling liquids; not watertight. Do not immerse in liquid or expose the pump to possible splash or sprayed liquids. |
| Electrical Classification | Type BF equipment with internal battery power source |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter InfusO.R. Pump User’s Manual.
The linked PDF is a Baxter Healthcare Corporation manufacturer manual, document 5371151, with cover marking 05/02 and an issue date of December 1998. Baxter currently maintains U.S. catalog records for standard product code 2L3100 and separate Baxter-refurbished product code 2L3100R. Verify the exact pump identifier, SMART LABEL, syringe, and administration-set configuration before use.
Baxter InfusO.R. Pump User’s Manual
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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