Brochure

B Braun Perfusor Space

The Perfusor Space Syringe Pump is the first syringe pump to include air and road transport in the 510(k) cleared indications for use. It is intended for use on adults, pediatrics, and neonates for the intermittent or continuous delivery of parenteral fluids, enteral fluids, medications, blood and blood products through clinically accepted routes of administration. These routes include intravenous, intra-arterial, subcutaneous, epidural and enteral.

The Perfusor Space Syringe Pump is intended to be used by trained healthcare professionals in healthcare facilities and air and/or road transport situations.

During design and validation, the device underwent more than 100 hours of usability testing with registered, practicing nurses and anesthesiologists.

Key Features:

• First syringe pump cleared with air and road transport in the indications for use.
• Wireless integration allows for complete interoperability.
• Integrated piston brake helps prevent inadvertent bolus during syringe change.
• Post-occlusion bolus reduction software designed to minimize bolus after occlusion.
• Automatic drive technology designed for accuracy and safety.
• A microprocessor in each pump allows for independent modularity, helping to prevent channel confusion and catastrophic pump failures.
• Compact design allows for vertical stacking in healthcare settings.
• KeyGuard™ non-numeric keypad with simple arrows intended to prevent manual programming errors related to zero vs. decimal entry
• DoseGuard™ Drug Library Development Software, powered by
• FDB Infusion Knowledge™, creates customizable drug limits and clinical advisories with confidence.
  • DoseTrac® Infusion Management Software allows for real-time pump infusion data reporting.

The Perfusor® Space® Syringe Pump is intended for use on adults, pediatrics, and neonates. It is the first syringe pump to receive FDA clearance for air and road transport. Weighing only 3 pounds, its compact design and flexible mounting positions allow for both vertical and horizontal delivery to accommodate IV and enteral infusions.

The Space pump design focuses on the needs of clinicians with an emphasis on intuitive workflow and navigation. To achieve this, B. Braun worked with Healthcare Human Factors, a global leader in developing best practices for human factors testing in healthcare. During validation, the device underwent extensive usability testing with registered, practicing nurses and anesthesiologists.

The first syringe pump cleared by the FDA for transport by air and road is the Infusomat Space syringe pump. This pump is designed with safety features to prevent inadvertent bolus during syringe change, as well as post-occlusion bolus reduction software to minimize bolus after occlusion. The pump is also flexible, supporting weight-based dosing limits as well as Patient Profiles with weight ranges. Additionally, the pump's independent modularity helps to prevent channel confusion and catastrophic pump failures. The pump is also designed for efficiency, with a lightweight and compact design that takes less space and can be stacked vertically for increased versatility in healthcare settings. Another unique feature of the Infusomat Space syringe pump is the KeyGuard, a non-numeric keypad with simple arrows that is designed to prevent manual programming errors by forcing the user to observe the screen during programming and making it impossible for errors such as zero vs decimal to occur. The pump also has a universal interface that is the same workflow as the Infusomat pump and an extensive drug library that includes customizable hard and soft limits and clinical advisories. Additionally, the pump is wireless and allows for complete interoperability. The pump also has a clearly visible alarm display with easily adjustable volume levels. Finally, the pump is MR conditional when used with the SpaceStation MRI, allowing for the uninterrupted delivery of medications to patients within the MRI suite.