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 Sigma Spectrum Infusion IV Pump Software 6.05
In stock
$997.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Compact single-channel volumetric smart infusion pump • Operating Software v6.05
- 0.5–999 mL/h • Master Drug Library with Dose Error Reduction System (DERS)
- Primary and secondary infusion • Multi-Step • Cyclic TPN • optional wireless connectivity on compatible hardware
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 6.05
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v6.05 is a compact single-channel volumetric smart pump designed for controlled administration of intravenous fluids and medication therapies. Its Gen 2 operating platform combines guided programming with a facility-controlled Master Drug Library and Dose Error Reduction System to support standardized medication programming and infusion-safety workflows.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v6.05
Product Description
Fully refurbished, biomed tested and calibrated by United Infusion, and backed by a 1-year warranty, the SIGMA Spectrum combines a linear-peristaltic pumping mechanism with a compact color display, guided programming, and configurable medication-safety functions.
Software v6.05 is a SIGMA Spectrum Gen 2 operating-software release. The manufacturer Operator’s Manual for this software is specified for use with MDL Editor v6.2.4. Master Drug Library content itself is pharmacy/facility controlled and can define care areas, drug concentrations, dosing modes, starting dose rates, soft and hard limits, bolus parameters, VTBI settings, and other infusion parameters.
Wireless functionality is configuration-dependent. Pumps equipped with a compatible Wireless Battery Module can receive drug-library transfers through an appropriately configured wireless network. P/N 35083 provides 802.11b connectivity. P/N 35162 provides 802.11b/g connectivity but is compatible only with Wireless G-compatible pumps, identified by a G preceding the pump serial number. Wireless capability should therefore be verified on the individual unit.
- Single-channel volumetric infusion pump
- Operating Software Version 6.05
- Master Drug Library with Dose Error Reduction System (DERS)
- Flow-rate range of 0.5–999 mL/h
- Primary and secondary infusion programming
- Automatic transition to the primary infusion after normal secondary completion unless Secondary Callback is active
- Configurable Secondary Callback with fixed 1 mL/h KVO at secondary completion when active
- Multi-Step programming with up to 10 individual infusion-rate steps
- Cyclic TPN infusion mode
- Loading Dose programming through DERS when enabled in the Drug Library
- Bolus programming in BASIC mode and optionally through DERS configuration
- Facility-configurable drug limits and care areas
- Color display with guided programming and on-board help
- Adjustable downstream occlusion-pressure settings
- Dual-beam ultrasonic air-in-line detection
- Set-based anti-free-flow protection using the IV-set slide clamp
- Optional 802.11b or 802.11b/g wireless connectivity on compatible hardware
- IrDA communication and external RS-232 support for applicable service/software functions
Specifications — Baxter SIGMA Spectrum Software 6.05
| Manufacturer | SIGMA / Baxter Healthcare |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Pump Models | 35700BAX / 35700ABB |
| Operating Software | Version 6.05 |
| Associated MDL Editor | Manufacturer Operator’s Manual specifies MDL Editor v6.2.4; deployed drug-library content and revision may vary by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Intravenous fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, intrathecal, epidural, and irrigation of fluid spaces when clinically appropriate and used according to manufacturer instructions |
| Flow Rate | 0.5–999 mL/h |
| Flow Rate Increments | 0.1 mL/h from 0.5–99.9 mL/h • 1 mL/h from 100–999 mL/h |
| Volumetric Accuracy — Baxter Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Volumetric Accuracy — Hospira Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–800 mL/h • ±10% from 801–999 mL/h under manufacturer-specified test conditions |
| Total Drug Delivered | 0.1–9999 mL; 0.1 mL increments from 0.1–99.9 mL and 1 mL increments from 100–9999 mL |
| Infusion Modes | Primary, Secondary, Multi-Step, and Cyclic TPN |
| Loading Dose | Available through DERS when enabled and configured for the selected drug in the Master Drug Library |
| Bolus | Bolus can always be delivered in BASIC mode and may be enabled/configured through DERS for individual Drug Library entries |
| Multi-Step | Supports programming of up to 10 individual infusion-rate steps |
| KVO — Primary Completion | Uses the drug-configured KVO rate or the current infusion rate, whichever is lower. Default KVO is 1 mL/h and can be configured from 0.5–50 mL/h. |
| Secondary Completion | Normally transitions automatically to the programmed primary infusion when secondary delivery completes unless Secondary Callback is active |
| Secondary Callback | May be configured as Required, Optional, or Never for a secondary drug. When active, the pump runs at a fixed 1 mL/h KVO rate after secondary completion and sounds an audio callback alarm. |
| Master Drug Library / DERS | Facility-controlled Master Drug Library supports care areas, concentrations, dose modes, starting rates, soft limits, optional hard limits, bolus settings, VTBI parameters, and related medication-programming controls |
| Air-in-Line Detection | Dual-beam ultrasonic detector; alarms for large bubbles and accumulated air according to manufacturer-defined thresholds |
| Downstream Occlusion | Adjustable Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Pump Pressure | 28 PSI |
| Automatic Occlusion Restart | Automatic restart occurs after a downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Compatible IV Sets | Compatible Baxter and Hospira standard gravity IV sets as identified in the manufacturer Operator’s Manual; set-specific accuracy and maximum-use limitations apply |
| Baxter Set Accuracy Duration | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Hospira Set Accuracy Duration | Specified accuracy maintained for up to 72 hours, maximum 9 liters, under manufacturer-specified conditions |
| Display | Color HRTFT display • 240 × 270 resolution • LED front-lit |
| Standard-Battery Dimensions | 5.8″ H × 4.2″ W × 2.5″ D without pole clamp • 5.8″ H × 6.4″ W × 4.7″ D with pole clamp |
| Wireless-Battery Dimensions | 6.3″ H × 4.2″ W × 2.5″ D without pole clamp • 6.3″ H × 6.4″ W × 4.7″ D with pole clamp |
| Standard-Battery Weight | 25.5 oz ±1 oz without pole clamp • 33.5 oz ±1 oz with pole clamp |
| Wireless-Battery Weight | 26.5 oz ±1 oz without pole clamp • 34.5 oz ±1 oz with pole clamp |
| Standard Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| 802.11b Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35083 • compatible with all SIGMA Spectrum pumps covered by the manufacturer documentation |
| 802.11b/g Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35162 • compatible only with Wireless G-compatible pumps identified by a “G” preceding the pump serial number |
| Wireless Battery Runtime | Approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Connectivity | Optional • IEEE 802.11b with P/N 35083 • IEEE 802.11b/g with P/N 35162 only on Wireless G-compatible pump hardware |
| Wireless Security | Supports documented WEP and WPA/WPA2/802.11i security configurations; available authentication options depend on wireless-module and network configuration |
| Drug Library Transfer | Wireless network transfer with a compatible Wireless Battery Module or direct PC-to-pump transfer through IrDA |
| External Interfaces | IrDA • asynchronous serial expansion interface • external RS-232 support for applicable software-upgrade functions |
| AC Adapter Input | 100–240 VAC • 50–60 Hz • 200 mA |
| AC Adapter P/N 35727 | 9 VDC / 1200 mA output • short-circuit protected |
| AC Adapter P/N 35714 | 9 VDC / 800 mA output • short-circuit protected |
| AC Adapter Cord | Approximately 3.0 m (9.75 ft) |
| Operating Conditions — Standard Battery | 60–90°F (15.6–32.2°C) • 20–90% RH noncondensing |
| Operating Conditions — Wireless Battery | 60–80°F (15.6–26.7°C) • 20–90% RH noncondensing |
| Storage Conditions | -4–120°F (-20–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA communications standards • IEEE 802.11b / 802.11b/g wireless standards as applicable • EIA-RS-232 asynchronous transmit/receive levels |
| Configuration | Drug-library content, care areas, dose limits, Secondary Callback, loading-dose and bolus settings, wireless capability, Wireless G compatibility, wireless security, alarms, infusion options, and other functions may vary according to the individual pump and facility configuration |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the SIGMA Spectrum Gen 2 Operator’s Manual for Software v6.05 and the Quick Start Guide for operating instructions, DERS programming, primary and secondary infusions, Multi-Step and Cyclic TPN modes, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Gen 2 — Operator’s Manual, Software v6.05
Download PDF
SIGMA Spectrum — Quick Start Guide
Download PDF
In stock
$997.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Compact single-channel volumetric smart infusion pump • Operating Software v6.05
- 0.5–999 mL/h • Master Drug Library with Dose Error Reduction System (DERS)
- Primary and secondary infusion • Multi-Step • Cyclic TPN • optional wireless connectivity on compatible hardware
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 6.05
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v6.05 is a compact single-channel volumetric smart pump designed for controlled administration of intravenous fluids and medication therapies. Its Gen 2 operating platform combines guided programming with a facility-controlled Master Drug Library and Dose Error Reduction System to support standardized medication programming and infusion-safety workflows.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v6.05
Product Description
Fully refurbished, biomed tested and calibrated by United Infusion, and backed by a 1-year warranty, the SIGMA Spectrum combines a linear-peristaltic pumping mechanism with a compact color display, guided programming, and configurable medication-safety functions.
Software v6.05 is a SIGMA Spectrum Gen 2 operating-software release. The manufacturer Operator’s Manual for this software is specified for use with MDL Editor v6.2.4. Master Drug Library content itself is pharmacy/facility controlled and can define care areas, drug concentrations, dosing modes, starting dose rates, soft and hard limits, bolus parameters, VTBI settings, and other infusion parameters.
Wireless functionality is configuration-dependent. Pumps equipped with a compatible Wireless Battery Module can receive drug-library transfers through an appropriately configured wireless network. P/N 35083 provides 802.11b connectivity. P/N 35162 provides 802.11b/g connectivity but is compatible only with Wireless G-compatible pumps, identified by a G preceding the pump serial number. Wireless capability should therefore be verified on the individual unit.
- Single-channel volumetric infusion pump
- Operating Software Version 6.05
- Master Drug Library with Dose Error Reduction System (DERS)
- Flow-rate range of 0.5–999 mL/h
- Primary and secondary infusion programming
- Automatic transition to the primary infusion after normal secondary completion unless Secondary Callback is active
- Configurable Secondary Callback with fixed 1 mL/h KVO at secondary completion when active
- Multi-Step programming with up to 10 individual infusion-rate steps
- Cyclic TPN infusion mode
- Loading Dose programming through DERS when enabled in the Drug Library
- Bolus programming in BASIC mode and optionally through DERS configuration
- Facility-configurable drug limits and care areas
- Color display with guided programming and on-board help
- Adjustable downstream occlusion-pressure settings
- Dual-beam ultrasonic air-in-line detection
- Set-based anti-free-flow protection using the IV-set slide clamp
- Optional 802.11b or 802.11b/g wireless connectivity on compatible hardware
- IrDA communication and external RS-232 support for applicable service/software functions
Specifications — Baxter SIGMA Spectrum Software 6.05
| Manufacturer | SIGMA / Baxter Healthcare |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Pump Models | 35700BAX / 35700ABB |
| Operating Software | Version 6.05 |
| Associated MDL Editor | Manufacturer Operator’s Manual specifies MDL Editor v6.2.4; deployed drug-library content and revision may vary by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Intravenous fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, intrathecal, epidural, and irrigation of fluid spaces when clinically appropriate and used according to manufacturer instructions |
| Flow Rate | 0.5–999 mL/h |
| Flow Rate Increments | 0.1 mL/h from 0.5–99.9 mL/h • 1 mL/h from 100–999 mL/h |
| Volumetric Accuracy — Baxter Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Volumetric Accuracy — Hospira Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–800 mL/h • ±10% from 801–999 mL/h under manufacturer-specified test conditions |
| Total Drug Delivered | 0.1–9999 mL; 0.1 mL increments from 0.1–99.9 mL and 1 mL increments from 100–9999 mL |
| Infusion Modes | Primary, Secondary, Multi-Step, and Cyclic TPN |
| Loading Dose | Available through DERS when enabled and configured for the selected drug in the Master Drug Library |
| Bolus | Bolus can always be delivered in BASIC mode and may be enabled/configured through DERS for individual Drug Library entries |
| Multi-Step | Supports programming of up to 10 individual infusion-rate steps |
| KVO — Primary Completion | Uses the drug-configured KVO rate or the current infusion rate, whichever is lower. Default KVO is 1 mL/h and can be configured from 0.5–50 mL/h. |
| Secondary Completion | Normally transitions automatically to the programmed primary infusion when secondary delivery completes unless Secondary Callback is active |
| Secondary Callback | May be configured as Required, Optional, or Never for a secondary drug. When active, the pump runs at a fixed 1 mL/h KVO rate after secondary completion and sounds an audio callback alarm. |
| Master Drug Library / DERS | Facility-controlled Master Drug Library supports care areas, concentrations, dose modes, starting rates, soft limits, optional hard limits, bolus settings, VTBI parameters, and related medication-programming controls |
| Air-in-Line Detection | Dual-beam ultrasonic detector; alarms for large bubbles and accumulated air according to manufacturer-defined thresholds |
| Downstream Occlusion | Adjustable Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Pump Pressure | 28 PSI |
| Automatic Occlusion Restart | Automatic restart occurs after a downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Compatible IV Sets | Compatible Baxter and Hospira standard gravity IV sets as identified in the manufacturer Operator’s Manual; set-specific accuracy and maximum-use limitations apply |
| Baxter Set Accuracy Duration | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Hospira Set Accuracy Duration | Specified accuracy maintained for up to 72 hours, maximum 9 liters, under manufacturer-specified conditions |
| Display | Color HRTFT display • 240 × 270 resolution • LED front-lit |
| Standard-Battery Dimensions | 5.8″ H × 4.2″ W × 2.5″ D without pole clamp • 5.8″ H × 6.4″ W × 4.7″ D with pole clamp |
| Wireless-Battery Dimensions | 6.3″ H × 4.2″ W × 2.5″ D without pole clamp • 6.3″ H × 6.4″ W × 4.7″ D with pole clamp |
| Standard-Battery Weight | 25.5 oz ±1 oz without pole clamp • 33.5 oz ±1 oz with pole clamp |
| Wireless-Battery Weight | 26.5 oz ±1 oz without pole clamp • 34.5 oz ±1 oz with pole clamp |
| Standard Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| 802.11b Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35083 • compatible with all SIGMA Spectrum pumps covered by the manufacturer documentation |
| 802.11b/g Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35162 • compatible only with Wireless G-compatible pumps identified by a “G” preceding the pump serial number |
| Wireless Battery Runtime | Approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Connectivity | Optional • IEEE 802.11b with P/N 35083 • IEEE 802.11b/g with P/N 35162 only on Wireless G-compatible pump hardware |
| Wireless Security | Supports documented WEP and WPA/WPA2/802.11i security configurations; available authentication options depend on wireless-module and network configuration |
| Drug Library Transfer | Wireless network transfer with a compatible Wireless Battery Module or direct PC-to-pump transfer through IrDA |
| External Interfaces | IrDA • asynchronous serial expansion interface • external RS-232 support for applicable software-upgrade functions |
| AC Adapter Input | 100–240 VAC • 50–60 Hz • 200 mA |
| AC Adapter P/N 35727 | 9 VDC / 1200 mA output • short-circuit protected |
| AC Adapter P/N 35714 | 9 VDC / 800 mA output • short-circuit protected |
| AC Adapter Cord | Approximately 3.0 m (9.75 ft) |
| Operating Conditions — Standard Battery | 60–90°F (15.6–32.2°C) • 20–90% RH noncondensing |
| Operating Conditions — Wireless Battery | 60–80°F (15.6–26.7°C) • 20–90% RH noncondensing |
| Storage Conditions | -4–120°F (-20–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA communications standards • IEEE 802.11b / 802.11b/g wireless standards as applicable • EIA-RS-232 asynchronous transmit/receive levels |
| Configuration | Drug-library content, care areas, dose limits, Secondary Callback, loading-dose and bolus settings, wireless capability, Wireless G compatibility, wireless security, alarms, infusion options, and other functions may vary according to the individual pump and facility configuration |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the SIGMA Spectrum Gen 2 Operator’s Manual for Software v6.05 and the Quick Start Guide for operating instructions, DERS programming, primary and secondary infusions, Multi-Step and Cyclic TPN modes, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Gen 2 — Operator’s Manual, Software v6.05
Download PDF
SIGMA Spectrum — Quick Start Guide
Download PDF
- Compact single-channel volumetric smart infusion pump • Operating Software v6.05
- 0.5–999 mL/h • Master Drug Library with Dose Error Reduction System (DERS)
- Primary and secondary infusion • Multi-Step • Cyclic TPN • optional wireless connectivity on compatible hardware
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 6.05
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v6.05 is a compact single-channel volumetric smart pump designed for controlled administration of intravenous fluids and medication therapies. Its Gen 2 operating platform combines guided programming with a facility-controlled Master Drug Library and Dose Error Reduction System to support standardized medication programming and infusion-safety workflows.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v6.05
Product Description
Fully refurbished, biomed tested and calibrated by United Infusion, and backed by a 1-year warranty, the SIGMA Spectrum combines a linear-peristaltic pumping mechanism with a compact color display, guided programming, and configurable medication-safety functions.
Software v6.05 is a SIGMA Spectrum Gen 2 operating-software release. The manufacturer Operator’s Manual for this software is specified for use with MDL Editor v6.2.4. Master Drug Library content itself is pharmacy/facility controlled and can define care areas, drug concentrations, dosing modes, starting dose rates, soft and hard limits, bolus parameters, VTBI settings, and other infusion parameters.
Wireless functionality is configuration-dependent. Pumps equipped with a compatible Wireless Battery Module can receive drug-library transfers through an appropriately configured wireless network. P/N 35083 provides 802.11b connectivity. P/N 35162 provides 802.11b/g connectivity but is compatible only with Wireless G-compatible pumps, identified by a G preceding the pump serial number. Wireless capability should therefore be verified on the individual unit.
- Single-channel volumetric infusion pump
- Operating Software Version 6.05
- Master Drug Library with Dose Error Reduction System (DERS)
- Flow-rate range of 0.5–999 mL/h
- Primary and secondary infusion programming
- Automatic transition to the primary infusion after normal secondary completion unless Secondary Callback is active
- Configurable Secondary Callback with fixed 1 mL/h KVO at secondary completion when active
- Multi-Step programming with up to 10 individual infusion-rate steps
- Cyclic TPN infusion mode
- Loading Dose programming through DERS when enabled in the Drug Library
- Bolus programming in BASIC mode and optionally through DERS configuration
- Facility-configurable drug limits and care areas
- Color display with guided programming and on-board help
- Adjustable downstream occlusion-pressure settings
- Dual-beam ultrasonic air-in-line detection
- Set-based anti-free-flow protection using the IV-set slide clamp
- Optional 802.11b or 802.11b/g wireless connectivity on compatible hardware
- IrDA communication and external RS-232 support for applicable service/software functions
Specifications — Baxter SIGMA Spectrum Software 6.05
| Manufacturer | SIGMA / Baxter Healthcare |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Pump Models | 35700BAX / 35700ABB |
| Operating Software | Version 6.05 |
| Associated MDL Editor | Manufacturer Operator’s Manual specifies MDL Editor v6.2.4; deployed drug-library content and revision may vary by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Intravenous fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, intrathecal, epidural, and irrigation of fluid spaces when clinically appropriate and used according to manufacturer instructions |
| Flow Rate | 0.5–999 mL/h |
| Flow Rate Increments | 0.1 mL/h from 0.5–99.9 mL/h • 1 mL/h from 100–999 mL/h |
| Volumetric Accuracy — Baxter Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Volumetric Accuracy — Hospira Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–800 mL/h • ±10% from 801–999 mL/h under manufacturer-specified test conditions |
| Total Drug Delivered | 0.1–9999 mL; 0.1 mL increments from 0.1–99.9 mL and 1 mL increments from 100–9999 mL |
| Infusion Modes | Primary, Secondary, Multi-Step, and Cyclic TPN |
| Loading Dose | Available through DERS when enabled and configured for the selected drug in the Master Drug Library |
| Bolus | Bolus can always be delivered in BASIC mode and may be enabled/configured through DERS for individual Drug Library entries |
| Multi-Step | Supports programming of up to 10 individual infusion-rate steps |
| KVO — Primary Completion | Uses the drug-configured KVO rate or the current infusion rate, whichever is lower. Default KVO is 1 mL/h and can be configured from 0.5–50 mL/h. |
| Secondary Completion | Normally transitions automatically to the programmed primary infusion when secondary delivery completes unless Secondary Callback is active |
| Secondary Callback | May be configured as Required, Optional, or Never for a secondary drug. When active, the pump runs at a fixed 1 mL/h KVO rate after secondary completion and sounds an audio callback alarm. |
| Master Drug Library / DERS | Facility-controlled Master Drug Library supports care areas, concentrations, dose modes, starting rates, soft limits, optional hard limits, bolus settings, VTBI parameters, and related medication-programming controls |
| Air-in-Line Detection | Dual-beam ultrasonic detector; alarms for large bubbles and accumulated air according to manufacturer-defined thresholds |
| Downstream Occlusion | Adjustable Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Pump Pressure | 28 PSI |
| Automatic Occlusion Restart | Automatic restart occurs after a downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Compatible IV Sets | Compatible Baxter and Hospira standard gravity IV sets as identified in the manufacturer Operator’s Manual; set-specific accuracy and maximum-use limitations apply |
| Baxter Set Accuracy Duration | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Hospira Set Accuracy Duration | Specified accuracy maintained for up to 72 hours, maximum 9 liters, under manufacturer-specified conditions |
| Display | Color HRTFT display • 240 × 270 resolution • LED front-lit |
| Standard-Battery Dimensions | 5.8″ H × 4.2″ W × 2.5″ D without pole clamp • 5.8″ H × 6.4″ W × 4.7″ D with pole clamp |
| Wireless-Battery Dimensions | 6.3″ H × 4.2″ W × 2.5″ D without pole clamp • 6.3″ H × 6.4″ W × 4.7″ D with pole clamp |
| Standard-Battery Weight | 25.5 oz ±1 oz without pole clamp • 33.5 oz ±1 oz with pole clamp |
| Wireless-Battery Weight | 26.5 oz ±1 oz without pole clamp • 34.5 oz ±1 oz with pole clamp |
| Standard Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| 802.11b Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35083 • compatible with all SIGMA Spectrum pumps covered by the manufacturer documentation |
| 802.11b/g Wireless Battery | Rechargeable Lithium-Ion • 1800 mAh • 7.4 VDC nominal • SIGMA P/N 35162 • compatible only with Wireless G-compatible pumps identified by a “G” preceding the pump serial number |
| Wireless Battery Runtime | Approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Connectivity | Optional • IEEE 802.11b with P/N 35083 • IEEE 802.11b/g with P/N 35162 only on Wireless G-compatible pump hardware |
| Wireless Security | Supports documented WEP and WPA/WPA2/802.11i security configurations; available authentication options depend on wireless-module and network configuration |
| Drug Library Transfer | Wireless network transfer with a compatible Wireless Battery Module or direct PC-to-pump transfer through IrDA |
| External Interfaces | IrDA • asynchronous serial expansion interface • external RS-232 support for applicable software-upgrade functions |
| AC Adapter Input | 100–240 VAC • 50–60 Hz • 200 mA |
| AC Adapter P/N 35727 | 9 VDC / 1200 mA output • short-circuit protected |
| AC Adapter P/N 35714 | 9 VDC / 800 mA output • short-circuit protected |
| AC Adapter Cord | Approximately 3.0 m (9.75 ft) |
| Operating Conditions — Standard Battery | 60–90°F (15.6–32.2°C) • 20–90% RH noncondensing |
| Operating Conditions — Wireless Battery | 60–80°F (15.6–26.7°C) • 20–90% RH noncondensing |
| Storage Conditions | -4–120°F (-20–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA communications standards • IEEE 802.11b / 802.11b/g wireless standards as applicable • EIA-RS-232 asynchronous transmit/receive levels |
| Configuration | Drug-library content, care areas, dose limits, Secondary Callback, loading-dose and bolus settings, wireless capability, Wireless G compatibility, wireless security, alarms, infusion options, and other functions may vary according to the individual pump and facility configuration |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the SIGMA Spectrum Gen 2 Operator’s Manual for Software v6.05 and the Quick Start Guide for operating instructions, DERS programming, primary and secondary infusions, Multi-Step and Cyclic TPN modes, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Gen 2 — Operator’s Manual, Software v6.05
Download PDF
SIGMA Spectrum — Quick Start Guide
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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