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 8.0
In stock
$1,097.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Compact single-channel volumetric smart infusion pump • Operating Software v8.00
- 0.5–999 mL/h • Master Drug Library Version 8 with Dose Error Reduction System (DERS)
- Primary and secondary • Multi-Step • Cyclic TPN • Amount/Time • optional wireless connectivity
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 8.0
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library Version 8 and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v8.00 is a compact single-channel volumetric smart infusion pump designed for controlled administration of fluids including medications, blood, blood products, and other compatible therapies. Software v8.00 works with Master Drug Library Version 8 and provides Dose Error Reduction System programming, guided workflows, multiple infusion modes, and configuration-dependent wireless drug-library management.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v8.00
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 color display, guided programming, configurable medication limits, and a facility-managed Master Drug Library.
Software v8.00 defaults to Dose Error Reduction System programming when a compatible Drug Library is installed. Drug records can include care areas, drug names and concentrations, programming modes, delivery bags, dose modes, starting rates, and configurable hard and soft limits. BASIC Mode remains available for non-DERS programming when clinically appropriate.
Software v8.00 supports Continuous Primary and Secondary infusion, Multi-Step, Cyclic TPN, and Amount/Time programming. Additional configurable functions include Loading Dose, Bolus, Secondary Callback, Delayed Run, Priming Volume adjustment, Line Flush, and automatic keypad locking. Availability and behavior of these features can depend on the facility’s Master Drug Library configuration.
Wireless capability is dependent on the battery module installed. Software v8.00 supports the Baxter P/N 35162 802.11b/g Wireless Battery Module for wireless Drug Library transfer and supported network communication. Drug Libraries can also be transferred directly from a compatible PC using IrDA.
- Single-channel linear-peristaltic volumetric infusion pump
- Operating Software Version 8.00
- Designed for use with Master Drug Library Version 8
- Dose Error Reduction System (DERS) programming
- Flow-rate range of 0.5–999 mL/h
- Continuous Primary and Secondary infusion modes
- Multi-Step programming with up to 10 individual steps
- Cyclic TPN programming
- Primary and Secondary Amount/Time infusion modes
- Loading Dose and Bolus programming
- Secondary Callback configurable as Required, Optional, or Never
- Delayed Run up to 12 hours when enabled through the Drug Library
- Priming Volume adjustment for applicable Amount/Time primary infusions
- Drug-Library-enabled Line Flush for applicable Amount/Time infusions
- Manual and Drug-Library-configurable automatic keypad locking
- Primary and Secondary Check Flow safety prompts
- Single-Step Rate or Dose Change alert
- Dual-beam ultrasonic air-in-line detection
- Adjustable downstream occlusion-pressure settings
- Set-based anti-free-flow protection using the IV-set slide clamp
- Minimum 4,500-event history-log capacity
- Optional 802.11b/g wireless connectivity with Baxter P/N 35162
- IrDA communication for direct Drug Library transfer
Specifications — Baxter SIGMA Spectrum Software 8.0
| Manufacturer | Baxter Healthcare Corporation / SIGMA |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Applicable Model / P/N | 35700BAX2 |
| Operating Software | Version 8.00 |
| Master Drug Library | Designed for use with Master Drug Library Version 8; deployed Drug Library content varies by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, 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 |
| Rate Accuracy — Baxter Standard IV Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Accuracy Duration — Baxter Standard Sets | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Total Volume | 0.1–9999 mL • 0.1 mL increments from 0.1–99.9 mL • 1 mL increments from 100–9999 mL |
| Infusion Delivery Modes | Continuous Primary and Secondary • Multi-Step • Cyclic TPN • Amount/Time Primary and Secondary |
| DERS | Dose Error Reduction System programming with facility-configured Master Drug Library hard and soft limits |
| BASIC Mode | Non-DERS continuous infusion programming when the desired drug or concentration is not available in the facility Drug Library |
| Loading Dose | Enabled and configured through the Master Drug Library; automatically transitions to the Primary infusion when complete |
| Bolus | Supported; automatically transitions to the Primary infusion rate after the programmed bolus completes |
| Multi-Step | Supports up to 10 individual programmed infusion steps |
| Cyclic TPN | Supports programmed ramp-up, main delivery, and taper-down therapy profiles |
| Amount/Time | Supported for both Primary and Secondary infusion programming |
| Delayed Run | When enabled per drug in the Master Drug Library, the start of a programmed infusion can be delayed for up to 12 hours |
| Priming Volume | Available for applicable Primary Amount/Time infusions during initial programming and IV-set load/reload; adjusts programmed volume calculations but does not physically prime the IV set |
| Line Flush | Drug-Library-enabled feature for applicable Amount/Time infusions • 1–100 mL configurable flush volume • may be repeated up to three times |
| KVO — Primary Completion | Uses the Drug-Library-configured KVO rate or current infusion rate, whichever is lower • default 1 mL/h • configurable from 0.5–50 mL/h |
| Secondary Completion | Automatically transitions to the programmed Primary infusion when Secondary Callback is not active |
| Secondary Callback | Configurable as Required, Optional, or Never through the Master Drug Library. When active at secondary completion, the pump runs at a fixed 1 mL/h KVO rate and provides an audio and visual notification. |
| Keypad Lock | Manual keypad locking supported; Auto Keypad Lock can be configured by Care Area in the Master Drug Library |
| History / Event Log | Minimum 4,500-event capacity; history can be filtered for system-error or drug-error events |
| Air-in-Line Detection | Dual-beam ultrasonic detector • detects large bubbles approximately greater than 140 µL in Baxter sets and accumulated-air conditions defined by the manufacturer |
| Downstream Occlusion | Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Allowable Pressure During Downstream Occlusion | 30 PSI (207 kPa) |
| Automatic Occlusion Restart | When enabled, automatic restart occurs after the downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Administration Sets | Uses compatible Baxter standard gravity IV administration sets; set-specific limitations and manufacturer instructions apply |
| Display | Color LCD with adjustable backlight |
| Standard-Battery Dimensions | Without pole clamp: 5.8″ H × 4.2″ W × 2.5″ D • With pole clamp: 5.8″ H × 6.6″ W × 4.7″ D |
| Wireless-Battery Dimensions | Without pole clamp: 6.3″ H × 4.2″ W × 2.5″ D • With pole clamp: 6.3″ H × 6.6″ W × 4.7″ D |
| 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 • 7.4 VDC nominal • Baxter P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 25 mL/h or 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| Wireless Battery Module | Rechargeable Lithium-Ion • 7.4 VDC nominal • 802.11b/g • Baxter P/N 35162 |
| Wireless Battery Runtime | Approximately 5 hours at 25 mL/h • approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Network | Optional IEEE 802.11b / 802.11g connectivity using Baxter Wireless Battery Module P/N 35162 |
| Wireless Frequency | 2.4 GHz |
| Wireless Security | WEP 64/128-bit • WPA/WPA2/802.11i • TKIP • CCMP/AES • WPA-PSK • 802.1X and documented enterprise authentication methods |
| Drug Library Transfer | Wireless network transfer when equipped with P/N 35162 Wireless Battery Module • direct PC-to-pump transfer through IrDA also supported |
| External Interface | IrDA using SIR Encoding Protocol |
| AC Power Adapter | Use Baxter P/N 35727 |
| AC Adapter Input | 115 VAC ±15% • 50–60 Hz • 300 mA maximum |
| AC Adapter Output | 9 VDC / 1200 mA • 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 | 14–120°F (-10–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Ingress Protection | IPX0; enclosure is not rated to protect against harmful water ingress |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA IrPHY v1.4 • IEEE 802.11b / 802.11g |
| Configuration | Drug Library content, care areas, dose modes, hard and soft limits, Loading Dose, Secondary Callback, Delayed Run, Line Flush, Priming Volume, Auto Keypad Lock, alarm settings, wireless capability, 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 Infusion System Operator’s Manual for Software v8.00 and the Quick Start Guide for operating instructions, DERS programming, Primary and Secondary infusions, Multi-Step, Cyclic TPN, Amount/Time, Loading Dose, Bolus, Delayed Run, Line Flush, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Infusion System — Operator’s Manual, Software v8.00
Download PDF
SIGMA Spectrum — Quick Start Guide
Download PDF
In stock
$1,097.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Compact single-channel volumetric smart infusion pump • Operating Software v8.00
- 0.5–999 mL/h • Master Drug Library Version 8 with Dose Error Reduction System (DERS)
- Primary and secondary • Multi-Step • Cyclic TPN • Amount/Time • optional wireless connectivity
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 8.0
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library Version 8 and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v8.00 is a compact single-channel volumetric smart infusion pump designed for controlled administration of fluids including medications, blood, blood products, and other compatible therapies. Software v8.00 works with Master Drug Library Version 8 and provides Dose Error Reduction System programming, guided workflows, multiple infusion modes, and configuration-dependent wireless drug-library management.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v8.00
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 color display, guided programming, configurable medication limits, and a facility-managed Master Drug Library.
Software v8.00 defaults to Dose Error Reduction System programming when a compatible Drug Library is installed. Drug records can include care areas, drug names and concentrations, programming modes, delivery bags, dose modes, starting rates, and configurable hard and soft limits. BASIC Mode remains available for non-DERS programming when clinically appropriate.
Software v8.00 supports Continuous Primary and Secondary infusion, Multi-Step, Cyclic TPN, and Amount/Time programming. Additional configurable functions include Loading Dose, Bolus, Secondary Callback, Delayed Run, Priming Volume adjustment, Line Flush, and automatic keypad locking. Availability and behavior of these features can depend on the facility’s Master Drug Library configuration.
Wireless capability is dependent on the battery module installed. Software v8.00 supports the Baxter P/N 35162 802.11b/g Wireless Battery Module for wireless Drug Library transfer and supported network communication. Drug Libraries can also be transferred directly from a compatible PC using IrDA.
- Single-channel linear-peristaltic volumetric infusion pump
- Operating Software Version 8.00
- Designed for use with Master Drug Library Version 8
- Dose Error Reduction System (DERS) programming
- Flow-rate range of 0.5–999 mL/h
- Continuous Primary and Secondary infusion modes
- Multi-Step programming with up to 10 individual steps
- Cyclic TPN programming
- Primary and Secondary Amount/Time infusion modes
- Loading Dose and Bolus programming
- Secondary Callback configurable as Required, Optional, or Never
- Delayed Run up to 12 hours when enabled through the Drug Library
- Priming Volume adjustment for applicable Amount/Time primary infusions
- Drug-Library-enabled Line Flush for applicable Amount/Time infusions
- Manual and Drug-Library-configurable automatic keypad locking
- Primary and Secondary Check Flow safety prompts
- Single-Step Rate or Dose Change alert
- Dual-beam ultrasonic air-in-line detection
- Adjustable downstream occlusion-pressure settings
- Set-based anti-free-flow protection using the IV-set slide clamp
- Minimum 4,500-event history-log capacity
- Optional 802.11b/g wireless connectivity with Baxter P/N 35162
- IrDA communication for direct Drug Library transfer
Specifications — Baxter SIGMA Spectrum Software 8.0
| Manufacturer | Baxter Healthcare Corporation / SIGMA |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Applicable Model / P/N | 35700BAX2 |
| Operating Software | Version 8.00 |
| Master Drug Library | Designed for use with Master Drug Library Version 8; deployed Drug Library content varies by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, 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 |
| Rate Accuracy — Baxter Standard IV Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Accuracy Duration — Baxter Standard Sets | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Total Volume | 0.1–9999 mL • 0.1 mL increments from 0.1–99.9 mL • 1 mL increments from 100–9999 mL |
| Infusion Delivery Modes | Continuous Primary and Secondary • Multi-Step • Cyclic TPN • Amount/Time Primary and Secondary |
| DERS | Dose Error Reduction System programming with facility-configured Master Drug Library hard and soft limits |
| BASIC Mode | Non-DERS continuous infusion programming when the desired drug or concentration is not available in the facility Drug Library |
| Loading Dose | Enabled and configured through the Master Drug Library; automatically transitions to the Primary infusion when complete |
| Bolus | Supported; automatically transitions to the Primary infusion rate after the programmed bolus completes |
| Multi-Step | Supports up to 10 individual programmed infusion steps |
| Cyclic TPN | Supports programmed ramp-up, main delivery, and taper-down therapy profiles |
| Amount/Time | Supported for both Primary and Secondary infusion programming |
| Delayed Run | When enabled per drug in the Master Drug Library, the start of a programmed infusion can be delayed for up to 12 hours |
| Priming Volume | Available for applicable Primary Amount/Time infusions during initial programming and IV-set load/reload; adjusts programmed volume calculations but does not physically prime the IV set |
| Line Flush | Drug-Library-enabled feature for applicable Amount/Time infusions • 1–100 mL configurable flush volume • may be repeated up to three times |
| KVO — Primary Completion | Uses the Drug-Library-configured KVO rate or current infusion rate, whichever is lower • default 1 mL/h • configurable from 0.5–50 mL/h |
| Secondary Completion | Automatically transitions to the programmed Primary infusion when Secondary Callback is not active |
| Secondary Callback | Configurable as Required, Optional, or Never through the Master Drug Library. When active at secondary completion, the pump runs at a fixed 1 mL/h KVO rate and provides an audio and visual notification. |
| Keypad Lock | Manual keypad locking supported; Auto Keypad Lock can be configured by Care Area in the Master Drug Library |
| History / Event Log | Minimum 4,500-event capacity; history can be filtered for system-error or drug-error events |
| Air-in-Line Detection | Dual-beam ultrasonic detector • detects large bubbles approximately greater than 140 µL in Baxter sets and accumulated-air conditions defined by the manufacturer |
| Downstream Occlusion | Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Allowable Pressure During Downstream Occlusion | 30 PSI (207 kPa) |
| Automatic Occlusion Restart | When enabled, automatic restart occurs after the downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Administration Sets | Uses compatible Baxter standard gravity IV administration sets; set-specific limitations and manufacturer instructions apply |
| Display | Color LCD with adjustable backlight |
| Standard-Battery Dimensions | Without pole clamp: 5.8″ H × 4.2″ W × 2.5″ D • With pole clamp: 5.8″ H × 6.6″ W × 4.7″ D |
| Wireless-Battery Dimensions | Without pole clamp: 6.3″ H × 4.2″ W × 2.5″ D • With pole clamp: 6.3″ H × 6.6″ W × 4.7″ D |
| 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 • 7.4 VDC nominal • Baxter P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 25 mL/h or 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| Wireless Battery Module | Rechargeable Lithium-Ion • 7.4 VDC nominal • 802.11b/g • Baxter P/N 35162 |
| Wireless Battery Runtime | Approximately 5 hours at 25 mL/h • approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Network | Optional IEEE 802.11b / 802.11g connectivity using Baxter Wireless Battery Module P/N 35162 |
| Wireless Frequency | 2.4 GHz |
| Wireless Security | WEP 64/128-bit • WPA/WPA2/802.11i • TKIP • CCMP/AES • WPA-PSK • 802.1X and documented enterprise authentication methods |
| Drug Library Transfer | Wireless network transfer when equipped with P/N 35162 Wireless Battery Module • direct PC-to-pump transfer through IrDA also supported |
| External Interface | IrDA using SIR Encoding Protocol |
| AC Power Adapter | Use Baxter P/N 35727 |
| AC Adapter Input | 115 VAC ±15% • 50–60 Hz • 300 mA maximum |
| AC Adapter Output | 9 VDC / 1200 mA • 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 | 14–120°F (-10–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Ingress Protection | IPX0; enclosure is not rated to protect against harmful water ingress |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA IrPHY v1.4 • IEEE 802.11b / 802.11g |
| Configuration | Drug Library content, care areas, dose modes, hard and soft limits, Loading Dose, Secondary Callback, Delayed Run, Line Flush, Priming Volume, Auto Keypad Lock, alarm settings, wireless capability, 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 Infusion System Operator’s Manual for Software v8.00 and the Quick Start Guide for operating instructions, DERS programming, Primary and Secondary infusions, Multi-Step, Cyclic TPN, Amount/Time, Loading Dose, Bolus, Delayed Run, Line Flush, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Infusion System — Operator’s Manual, Software v8.00
Download PDF
SIGMA Spectrum — Quick Start Guide
Download PDF
- Compact single-channel volumetric smart infusion pump • Operating Software v8.00
- 0.5–999 mL/h • Master Drug Library Version 8 with Dose Error Reduction System (DERS)
- Primary and secondary • Multi-Step • Cyclic TPN • Amount/Time • optional wireless connectivity
Refurbished Baxter SIGMA Spectrum Infusion IV Pump Software 8.0
Refurbished • 1-Year Warranty • Single-channel smart volumetric infusion pump with Master Drug Library Version 8 and DERS
The Baxter SIGMA Spectrum Infusion Pump with Software v8.00 is a compact single-channel volumetric smart infusion pump designed for controlled administration of fluids including medications, blood, blood products, and other compatible therapies. Software v8.00 works with Master Drug Library Version 8 and provides Dose Error Reduction System programming, guided workflows, multiple infusion modes, and configuration-dependent wireless drug-library management.
What’s Included
- 1× Baxter SIGMA Spectrum Infusion Pump with Operating Software v8.00
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 color display, guided programming, configurable medication limits, and a facility-managed Master Drug Library.
Software v8.00 defaults to Dose Error Reduction System programming when a compatible Drug Library is installed. Drug records can include care areas, drug names and concentrations, programming modes, delivery bags, dose modes, starting rates, and configurable hard and soft limits. BASIC Mode remains available for non-DERS programming when clinically appropriate.
Software v8.00 supports Continuous Primary and Secondary infusion, Multi-Step, Cyclic TPN, and Amount/Time programming. Additional configurable functions include Loading Dose, Bolus, Secondary Callback, Delayed Run, Priming Volume adjustment, Line Flush, and automatic keypad locking. Availability and behavior of these features can depend on the facility’s Master Drug Library configuration.
Wireless capability is dependent on the battery module installed. Software v8.00 supports the Baxter P/N 35162 802.11b/g Wireless Battery Module for wireless Drug Library transfer and supported network communication. Drug Libraries can also be transferred directly from a compatible PC using IrDA.
- Single-channel linear-peristaltic volumetric infusion pump
- Operating Software Version 8.00
- Designed for use with Master Drug Library Version 8
- Dose Error Reduction System (DERS) programming
- Flow-rate range of 0.5–999 mL/h
- Continuous Primary and Secondary infusion modes
- Multi-Step programming with up to 10 individual steps
- Cyclic TPN programming
- Primary and Secondary Amount/Time infusion modes
- Loading Dose and Bolus programming
- Secondary Callback configurable as Required, Optional, or Never
- Delayed Run up to 12 hours when enabled through the Drug Library
- Priming Volume adjustment for applicable Amount/Time primary infusions
- Drug-Library-enabled Line Flush for applicable Amount/Time infusions
- Manual and Drug-Library-configurable automatic keypad locking
- Primary and Secondary Check Flow safety prompts
- Single-Step Rate or Dose Change alert
- Dual-beam ultrasonic air-in-line detection
- Adjustable downstream occlusion-pressure settings
- Set-based anti-free-flow protection using the IV-set slide clamp
- Minimum 4,500-event history-log capacity
- Optional 802.11b/g wireless connectivity with Baxter P/N 35162
- IrDA communication for direct Drug Library transfer
Specifications — Baxter SIGMA Spectrum Software 8.0
| Manufacturer | Baxter Healthcare Corporation / SIGMA |
| Product | SIGMA Spectrum Infusion Pump with Master Drug Library |
| Applicable Model / P/N | 35700BAX2 |
| Operating Software | Version 8.00 |
| Master Drug Library | Designed for use with Master Drug Library Version 8; deployed Drug Library content varies by facility |
| Type | Single-channel volumetric smart infusion pump |
| Pumping Mechanism | Linear peristaltic |
| Intended Fluids | Fluids including pharmaceutical drugs, blood, blood products, and mixtures required for patient therapy when used according to manufacturer instructions |
| Delivery Routes | Intravenous, arterial, subcutaneous, 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 |
| Rate Accuracy — Baxter Standard IV Sets | ±0.1 mL/h from 0.5–1.9 mL/h • ±5% from 2–999 mL/h under manufacturer-specified test conditions |
| Accuracy Duration — Baxter Standard Sets | Specified accuracy maintained for up to 96 hours, maximum 12 liters, under manufacturer-specified conditions |
| Total Volume | 0.1–9999 mL • 0.1 mL increments from 0.1–99.9 mL • 1 mL increments from 100–9999 mL |
| Infusion Delivery Modes | Continuous Primary and Secondary • Multi-Step • Cyclic TPN • Amount/Time Primary and Secondary |
| DERS | Dose Error Reduction System programming with facility-configured Master Drug Library hard and soft limits |
| BASIC Mode | Non-DERS continuous infusion programming when the desired drug or concentration is not available in the facility Drug Library |
| Loading Dose | Enabled and configured through the Master Drug Library; automatically transitions to the Primary infusion when complete |
| Bolus | Supported; automatically transitions to the Primary infusion rate after the programmed bolus completes |
| Multi-Step | Supports up to 10 individual programmed infusion steps |
| Cyclic TPN | Supports programmed ramp-up, main delivery, and taper-down therapy profiles |
| Amount/Time | Supported for both Primary and Secondary infusion programming |
| Delayed Run | When enabled per drug in the Master Drug Library, the start of a programmed infusion can be delayed for up to 12 hours |
| Priming Volume | Available for applicable Primary Amount/Time infusions during initial programming and IV-set load/reload; adjusts programmed volume calculations but does not physically prime the IV set |
| Line Flush | Drug-Library-enabled feature for applicable Amount/Time infusions • 1–100 mL configurable flush volume • may be repeated up to three times |
| KVO — Primary Completion | Uses the Drug-Library-configured KVO rate or current infusion rate, whichever is lower • default 1 mL/h • configurable from 0.5–50 mL/h |
| Secondary Completion | Automatically transitions to the programmed Primary infusion when Secondary Callback is not active |
| Secondary Callback | Configurable as Required, Optional, or Never through the Master Drug Library. When active at secondary completion, the pump runs at a fixed 1 mL/h KVO rate and provides an audio and visual notification. |
| Keypad Lock | Manual keypad locking supported; Auto Keypad Lock can be configured by Care Area in the Master Drug Library |
| History / Event Log | Minimum 4,500-event capacity; history can be filtered for system-error or drug-error events |
| Air-in-Line Detection | Dual-beam ultrasonic detector • detects large bubbles approximately greater than 140 µL in Baxter sets and accumulated-air conditions defined by the manufacturer |
| Downstream Occlusion | Low 6 ±4 PSI • Medium 13 ±6 PSI • High 19 ±9 PSI |
| Maximum Allowable Pressure During Downstream Occlusion | 30 PSI (207 kPa) |
| Automatic Occlusion Restart | When enabled, automatic restart occurs after the downstream occlusion is cleared |
| Anti-Free-Flow System | Set-based protection utilizing the IV administration-set slide clamp |
| Administration Sets | Uses compatible Baxter standard gravity IV administration sets; set-specific limitations and manufacturer instructions apply |
| Display | Color LCD with adjustable backlight |
| Standard-Battery Dimensions | Without pole clamp: 5.8″ H × 4.2″ W × 2.5″ D • With pole clamp: 5.8″ H × 6.6″ W × 4.7″ D |
| Wireless-Battery Dimensions | Without pole clamp: 6.3″ H × 4.2″ W × 2.5″ D • With pole clamp: 6.3″ H × 6.6″ W × 4.7″ D |
| 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 • 7.4 VDC nominal • Baxter P/N 35724 |
| Standard Battery Runtime | Approximately 8 hours at 25 mL/h or 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Standard Battery Recharge | Approximately 12 hours |
| Wireless Battery Module | Rechargeable Lithium-Ion • 7.4 VDC nominal • 802.11b/g • Baxter P/N 35162 |
| Wireless Battery Runtime | Approximately 5 hours at 25 mL/h • approximately 4 hours at 125 mL/h with the highest backlight setting under manufacturer-specified conditions |
| Wireless Battery Recharge | Approximately 16 hours |
| Wireless Network | Optional IEEE 802.11b / 802.11g connectivity using Baxter Wireless Battery Module P/N 35162 |
| Wireless Frequency | 2.4 GHz |
| Wireless Security | WEP 64/128-bit • WPA/WPA2/802.11i • TKIP • CCMP/AES • WPA-PSK • 802.1X and documented enterprise authentication methods |
| Drug Library Transfer | Wireless network transfer when equipped with P/N 35162 Wireless Battery Module • direct PC-to-pump transfer through IrDA also supported |
| External Interface | IrDA using SIR Encoding Protocol |
| AC Power Adapter | Use Baxter P/N 35727 |
| AC Adapter Input | 115 VAC ±15% • 50–60 Hz • 300 mA maximum |
| AC Adapter Output | 9 VDC / 1200 mA • 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 | 14–120°F (-10–49°C) • 10–90% RH noncondensing |
| Electrical Classification | Class II equipment • Type BF applied part • Continuous operation |
| Ingress Protection | IPX0; enclosure is not rated to protect against harmful water ingress |
| Standards | IEC 60601-1 including applicable collateral standards • IrDA IrPHY v1.4 • IEEE 802.11b / 802.11g |
| Configuration | Drug Library content, care areas, dose modes, hard and soft limits, Loading Dose, Secondary Callback, Delayed Run, Line Flush, Priming Volume, Auto Keypad Lock, alarm settings, wireless capability, 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 Infusion System Operator’s Manual for Software v8.00 and the Quick Start Guide for operating instructions, DERS programming, Primary and Secondary infusions, Multi-Step, Cyclic TPN, Amount/Time, Loading Dose, Bolus, Delayed Run, Line Flush, wireless operation, alarms, technical specifications, maintenance, and safety information.
SIGMA Spectrum Infusion System — Operator’s Manual, Software v8.00
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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!!!"
Need a quote, service help, or a similar model?
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