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 Flo-gard 6201 Infusion IV Pump
In stock
$695.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Single-channel linear peristaltic volumetric infusion pump for primary and secondary IV therapy
- Primary flow rate up to 1999 mL/h • secondary flow rate up to 999 mL/h • VTBI up to 9999 mL
- Supports blood and fat emulsions • ultrasonic air-in-line detection • upstream and downstream occlusion sensing
Refurbished Baxter Flo-Gard 6201 Infusion IV Pump
Refurbished • 1-Year Warranty • Single-channel volumetric infusion pump with primary, secondary, and programmed-delivery capabilities
The Baxter Flo-Gard 6201 Volumetric Infusion Pump is a single-channel linear peristaltic infusion system designed to deliver a wide variety of fluids over a broad range of infusion rates. It supports primary and secondary infusion programs, Volume-Time programming, and Programmed Delivery Profiles while using compatible Baxter “s” designated administration sets. The pump is capable of delivering fluids including blood and fat emulsions and is suitable for appropriately indicated epidural administration when used according to Baxter instructions.
What’s Included
- 1× Baxter Flo-Gard 6201 Volumetric Infusion Pump
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Baxter Flo-Gard 6201 provides primary and secondary volumetric infusion capability in a standalone pole-mounted pump. The secondary medication program automatically returns to the primary program after the programmed secondary VTBI has been delivered.
Safety features include upstream and downstream occlusion sensing, an ultrasonic air-in-line detector, an automatic safety clamp that occludes the tubing when the pump door is opened, configurable downstream occlusion sensitivity, and a locking control panel. The pump also supports Volume-Time programming and Programmed Delivery Profiles for therapies requiring multiple programmed flow rates.
- Single-channel linear peristaltic volumetric infusion pump
- Primary infusion rate up to 1999 mL/h
- Secondary infusion rate up to 999 mL/h
- Primary and secondary VTBI programming up to 9999 mL
- Ultrasonic air-in-line detection and upstream/downstream occlusion sensing
- Approximately 6 hours of battery operation under manufacturer-specified conditions
Specifications — Baxter Flo-Gard 6201 Volumetric Infusion Pump
| Manufacturer | Baxter Healthcare Corporation |
| Product | Flo-Gard 6201 Volumetric Infusion Pump |
| Model | 6201 |
| Catalog Code | 2M8063 — manufacturer Operator’s Manual reference |
| Type | Single-channel volumetric infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Administration Sets | Baxter “s” designated administration sets |
| Primary Flow Rate Range | 1–1999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 1999 mL/h |
| Secondary Flow Rate Range | 1–999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 999 mL/h |
| Maximum Flow Configuration | Maximum programmable flow rate can be configured from 1–1999 mL/h and may be reduced by authorized service personnel |
| VTBI Range | 1–9999 mL for both primary and secondary programs; 0.1 mL increments available from 1.0–99.9 mL and 1 mL increments through 9999 mL |
| KVO Rate | 5 mL/h or the programmed rate, whichever is less |
| Primary / Secondary Programming | Independent secondary medication program automatically switches back to the primary program when the secondary VTBI is completed |
| Volume-Time Programming | User programs the VTBI and delivery time; the pump automatically calculates the required flow rate within its allowable range |
| Programmed Delivery Profile | Supports manual or ramped programming of up to 10 sequential infusion programs, subject to installed software and pump configuration |
| Ramp PDP Total VTBI | 100–9999 mL for run times up to 16 hours; 200–9999 mL for run times greater than 16 hours |
| Ramp PDP Delay Time | 00:00–08:00 hours in 1-minute increments |
| Ramp PDP Run Time | 01:00–24:00 hours in 1-minute increments |
| Fluid Compatibility | Designed to pump a wide variety of fluids including blood and fat emulsions when used with appropriate Baxter administration sets |
| Epidural Use | Suitable for appropriately indicated epidural administration subject to Baxter’s specific drug, catheter, duration, and administration-set precautions |
| Air-in-Line Detection | Ultrasonic detector; factory NORM configuration alarms at approximately 75 µL or larger, while MIN configuration alarms at approximately 50 µL or larger |
| Occlusion Detection | Upstream and downstream occlusion sensors; downstream sensitivity is configurable |
| Downstream Occlusion Levels | Level 1: approximately 7 psig • Level 2: approximately 12 psig • Level 3: approximately 17 psig |
| Automatic Restart | Configurable for 0–9 automatic restarts after a downstream occlusion is relieved; configuration should be verified on the individual pump |
| Safety Clamp | Automatically occludes the tubing when the pump door is opened |
| Control Panel Lock | Rear-panel lock can disable front-panel programming controls while retaining specified display functions |
| Infusion Memory | Approximately 5-hour memory retains infusion data after power-off |
| Communications | RS-232C communications port for compatible computer monitoring or control |
| Nurse Call | Available through the communications port |
| Battery | 12 V, 2.0 Ah sealed lead-acid battery |
| Battery Runtime | Approximately 6 hours with the pump operating from 1–1400 mL/h under manufacturer-specified conditions |
| Battery Recharge | Approximately 8 hours for more than 80% recharge |
| AC Power | 110/120 V AC, 60 Hz |
| Power Cord | Approximately 9.5 ft (2.9 m), hospital-grade plug |
| Dimensions | 7.9″ W × 5.1″ D × 11.4″ H (20 × 13 × 29 cm) |
| Weight | Approximately 11.6 lb (5.3 kg) |
| Configuration | Several pump features and maximum programming limits are configurable; settings should be verified on the individual unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter Flo-Gard 6201 Operator’s Manual for operating instructions, programming, alarms, configuration options, technical specifications, and safety precautions. Verify the individual pump’s configuration and compatible Baxter administration set before clinical use.
Flo-Gard 6201 Volumetric Infusion Pump Operator’s Manual
Download PDF
In stock
$695.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Single-channel linear peristaltic volumetric infusion pump for primary and secondary IV therapy
- Primary flow rate up to 1999 mL/h • secondary flow rate up to 999 mL/h • VTBI up to 9999 mL
- Supports blood and fat emulsions • ultrasonic air-in-line detection • upstream and downstream occlusion sensing
Refurbished Baxter Flo-Gard 6201 Infusion IV Pump
Refurbished • 1-Year Warranty • Single-channel volumetric infusion pump with primary, secondary, and programmed-delivery capabilities
The Baxter Flo-Gard 6201 Volumetric Infusion Pump is a single-channel linear peristaltic infusion system designed to deliver a wide variety of fluids over a broad range of infusion rates. It supports primary and secondary infusion programs, Volume-Time programming, and Programmed Delivery Profiles while using compatible Baxter “s” designated administration sets. The pump is capable of delivering fluids including blood and fat emulsions and is suitable for appropriately indicated epidural administration when used according to Baxter instructions.
What’s Included
- 1× Baxter Flo-Gard 6201 Volumetric Infusion Pump
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Baxter Flo-Gard 6201 provides primary and secondary volumetric infusion capability in a standalone pole-mounted pump. The secondary medication program automatically returns to the primary program after the programmed secondary VTBI has been delivered.
Safety features include upstream and downstream occlusion sensing, an ultrasonic air-in-line detector, an automatic safety clamp that occludes the tubing when the pump door is opened, configurable downstream occlusion sensitivity, and a locking control panel. The pump also supports Volume-Time programming and Programmed Delivery Profiles for therapies requiring multiple programmed flow rates.
- Single-channel linear peristaltic volumetric infusion pump
- Primary infusion rate up to 1999 mL/h
- Secondary infusion rate up to 999 mL/h
- Primary and secondary VTBI programming up to 9999 mL
- Ultrasonic air-in-line detection and upstream/downstream occlusion sensing
- Approximately 6 hours of battery operation under manufacturer-specified conditions
Specifications — Baxter Flo-Gard 6201 Volumetric Infusion Pump
| Manufacturer | Baxter Healthcare Corporation |
| Product | Flo-Gard 6201 Volumetric Infusion Pump |
| Model | 6201 |
| Catalog Code | 2M8063 — manufacturer Operator’s Manual reference |
| Type | Single-channel volumetric infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Administration Sets | Baxter “s” designated administration sets |
| Primary Flow Rate Range | 1–1999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 1999 mL/h |
| Secondary Flow Rate Range | 1–999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 999 mL/h |
| Maximum Flow Configuration | Maximum programmable flow rate can be configured from 1–1999 mL/h and may be reduced by authorized service personnel |
| VTBI Range | 1–9999 mL for both primary and secondary programs; 0.1 mL increments available from 1.0–99.9 mL and 1 mL increments through 9999 mL |
| KVO Rate | 5 mL/h or the programmed rate, whichever is less |
| Primary / Secondary Programming | Independent secondary medication program automatically switches back to the primary program when the secondary VTBI is completed |
| Volume-Time Programming | User programs the VTBI and delivery time; the pump automatically calculates the required flow rate within its allowable range |
| Programmed Delivery Profile | Supports manual or ramped programming of up to 10 sequential infusion programs, subject to installed software and pump configuration |
| Ramp PDP Total VTBI | 100–9999 mL for run times up to 16 hours; 200–9999 mL for run times greater than 16 hours |
| Ramp PDP Delay Time | 00:00–08:00 hours in 1-minute increments |
| Ramp PDP Run Time | 01:00–24:00 hours in 1-minute increments |
| Fluid Compatibility | Designed to pump a wide variety of fluids including blood and fat emulsions when used with appropriate Baxter administration sets |
| Epidural Use | Suitable for appropriately indicated epidural administration subject to Baxter’s specific drug, catheter, duration, and administration-set precautions |
| Air-in-Line Detection | Ultrasonic detector; factory NORM configuration alarms at approximately 75 µL or larger, while MIN configuration alarms at approximately 50 µL or larger |
| Occlusion Detection | Upstream and downstream occlusion sensors; downstream sensitivity is configurable |
| Downstream Occlusion Levels | Level 1: approximately 7 psig • Level 2: approximately 12 psig • Level 3: approximately 17 psig |
| Automatic Restart | Configurable for 0–9 automatic restarts after a downstream occlusion is relieved; configuration should be verified on the individual pump |
| Safety Clamp | Automatically occludes the tubing when the pump door is opened |
| Control Panel Lock | Rear-panel lock can disable front-panel programming controls while retaining specified display functions |
| Infusion Memory | Approximately 5-hour memory retains infusion data after power-off |
| Communications | RS-232C communications port for compatible computer monitoring or control |
| Nurse Call | Available through the communications port |
| Battery | 12 V, 2.0 Ah sealed lead-acid battery |
| Battery Runtime | Approximately 6 hours with the pump operating from 1–1400 mL/h under manufacturer-specified conditions |
| Battery Recharge | Approximately 8 hours for more than 80% recharge |
| AC Power | 110/120 V AC, 60 Hz |
| Power Cord | Approximately 9.5 ft (2.9 m), hospital-grade plug |
| Dimensions | 7.9″ W × 5.1″ D × 11.4″ H (20 × 13 × 29 cm) |
| Weight | Approximately 11.6 lb (5.3 kg) |
| Configuration | Several pump features and maximum programming limits are configurable; settings should be verified on the individual unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter Flo-Gard 6201 Operator’s Manual for operating instructions, programming, alarms, configuration options, technical specifications, and safety precautions. Verify the individual pump’s configuration and compatible Baxter administration set before clinical use.
Flo-Gard 6201 Volumetric Infusion Pump Operator’s Manual
Download PDF
- Single-channel linear peristaltic volumetric infusion pump for primary and secondary IV therapy
- Primary flow rate up to 1999 mL/h • secondary flow rate up to 999 mL/h • VTBI up to 9999 mL
- Supports blood and fat emulsions • ultrasonic air-in-line detection • upstream and downstream occlusion sensing
Refurbished Baxter Flo-Gard 6201 Infusion IV Pump
Refurbished • 1-Year Warranty • Single-channel volumetric infusion pump with primary, secondary, and programmed-delivery capabilities
The Baxter Flo-Gard 6201 Volumetric Infusion Pump is a single-channel linear peristaltic infusion system designed to deliver a wide variety of fluids over a broad range of infusion rates. It supports primary and secondary infusion programs, Volume-Time programming, and Programmed Delivery Profiles while using compatible Baxter “s” designated administration sets. The pump is capable of delivering fluids including blood and fat emulsions and is suitable for appropriately indicated epidural administration when used according to Baxter instructions.
What’s Included
- 1× Baxter Flo-Gard 6201 Volumetric Infusion Pump
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, the Baxter Flo-Gard 6201 provides primary and secondary volumetric infusion capability in a standalone pole-mounted pump. The secondary medication program automatically returns to the primary program after the programmed secondary VTBI has been delivered.
Safety features include upstream and downstream occlusion sensing, an ultrasonic air-in-line detector, an automatic safety clamp that occludes the tubing when the pump door is opened, configurable downstream occlusion sensitivity, and a locking control panel. The pump also supports Volume-Time programming and Programmed Delivery Profiles for therapies requiring multiple programmed flow rates.
- Single-channel linear peristaltic volumetric infusion pump
- Primary infusion rate up to 1999 mL/h
- Secondary infusion rate up to 999 mL/h
- Primary and secondary VTBI programming up to 9999 mL
- Ultrasonic air-in-line detection and upstream/downstream occlusion sensing
- Approximately 6 hours of battery operation under manufacturer-specified conditions
Specifications — Baxter Flo-Gard 6201 Volumetric Infusion Pump
| Manufacturer | Baxter Healthcare Corporation |
| Product | Flo-Gard 6201 Volumetric Infusion Pump |
| Model | 6201 |
| Catalog Code | 2M8063 — manufacturer Operator’s Manual reference |
| Type | Single-channel volumetric infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Administration Sets | Baxter “s” designated administration sets |
| Primary Flow Rate Range | 1–1999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 1999 mL/h |
| Secondary Flow Rate Range | 1–999 mL/h maximum; 0.1 mL/h programming increments are available from 1.0–99.9 mL/h and 1 mL/h increments are available through 999 mL/h |
| Maximum Flow Configuration | Maximum programmable flow rate can be configured from 1–1999 mL/h and may be reduced by authorized service personnel |
| VTBI Range | 1–9999 mL for both primary and secondary programs; 0.1 mL increments available from 1.0–99.9 mL and 1 mL increments through 9999 mL |
| KVO Rate | 5 mL/h or the programmed rate, whichever is less |
| Primary / Secondary Programming | Independent secondary medication program automatically switches back to the primary program when the secondary VTBI is completed |
| Volume-Time Programming | User programs the VTBI and delivery time; the pump automatically calculates the required flow rate within its allowable range |
| Programmed Delivery Profile | Supports manual or ramped programming of up to 10 sequential infusion programs, subject to installed software and pump configuration |
| Ramp PDP Total VTBI | 100–9999 mL for run times up to 16 hours; 200–9999 mL for run times greater than 16 hours |
| Ramp PDP Delay Time | 00:00–08:00 hours in 1-minute increments |
| Ramp PDP Run Time | 01:00–24:00 hours in 1-minute increments |
| Fluid Compatibility | Designed to pump a wide variety of fluids including blood and fat emulsions when used with appropriate Baxter administration sets |
| Epidural Use | Suitable for appropriately indicated epidural administration subject to Baxter’s specific drug, catheter, duration, and administration-set precautions |
| Air-in-Line Detection | Ultrasonic detector; factory NORM configuration alarms at approximately 75 µL or larger, while MIN configuration alarms at approximately 50 µL or larger |
| Occlusion Detection | Upstream and downstream occlusion sensors; downstream sensitivity is configurable |
| Downstream Occlusion Levels | Level 1: approximately 7 psig • Level 2: approximately 12 psig • Level 3: approximately 17 psig |
| Automatic Restart | Configurable for 0–9 automatic restarts after a downstream occlusion is relieved; configuration should be verified on the individual pump |
| Safety Clamp | Automatically occludes the tubing when the pump door is opened |
| Control Panel Lock | Rear-panel lock can disable front-panel programming controls while retaining specified display functions |
| Infusion Memory | Approximately 5-hour memory retains infusion data after power-off |
| Communications | RS-232C communications port for compatible computer monitoring or control |
| Nurse Call | Available through the communications port |
| Battery | 12 V, 2.0 Ah sealed lead-acid battery |
| Battery Runtime | Approximately 6 hours with the pump operating from 1–1400 mL/h under manufacturer-specified conditions |
| Battery Recharge | Approximately 8 hours for more than 80% recharge |
| AC Power | 110/120 V AC, 60 Hz |
| Power Cord | Approximately 9.5 ft (2.9 m), hospital-grade plug |
| Dimensions | 7.9″ W × 5.1″ D × 11.4″ H (20 × 13 × 29 cm) |
| Weight | Approximately 11.6 lb (5.3 kg) |
| Configuration | Several pump features and maximum programming limits are configurable; settings should be verified on the individual unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the Baxter Flo-Gard 6201 Operator’s Manual for operating instructions, programming, alarms, configuration options, technical specifications, and safety precautions. Verify the individual pump’s configuration and compatible Baxter administration set before clinical use.
Flo-Gard 6201 Volumetric Infusion Pump Operator’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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