ExactaMix PRO
expands on the ExactaMix legacy and is the first and only automated compounder that is cyber secure.*
*Certified to the FDA-recognized cybersecurity standard, UL 2900-2-1.
This site is intended for Healthcare Professionals only. All products may not be available in all countries. Contact your local Baxter representative.
Important Safety InformationExplore how we advance Clinical Nutrition in a variety of therapeutic areas
This site is intended for Healthcare Professionals only. All products may not be available in all countries. Contact your local Baxter representative.
Important Safety Informationexpands on the ExactaMix legacy and is the first and only automated compounder that is cyber secure.*
*Certified to the FDA-recognized cybersecurity standard, UL 2900-2-1.
When pre-mixed nutrient solutions cannot match a patient’s specific needs, a customized approach is called for.1 Hospital pharmacies can compound PN solutions manually, but this can be labor-intensive, has high potential for error and may be difficult to do consistently.2,3 Automated compounding helps reduce these risks with better process control and less variation while improving safety, efficiency and cost.3,4 As compared to manual processes, the use of an automated compounder has been shown to reduce time per solution by 40%.5
Of innovating in PN compounding
Hospital pharmacies and compounding centers worldwide use ExactaMix
Nutritional bags compounded with ExactaMix
In meeting the evolving needs of the modern pharmacy, ExactaMix delivers automated compounding allowing for greater efficiencies compared to manual compounding.
Flexible
- Accommodates pharmacies’ individual needs regarding ingredients, approval and reporting
- Compound TPN, CRRT, cardioplegia, base solutions and epidurals
- Self-contained system can interface with pharmacy TPN order entry systems
- Made to adapt to the demands of individual pharmacies, providing flexibility in amount of ingredients, approval and reporting
- 24 ports minimize the need for manual ingredient additions
Accurate
- Transfer volumes as low as 0.2 mL
- Volumetric delivery followed by gravimetric check
Efficient and safety features
- Barcode scanner
- 14 reports available to support patient documentation and USP <797> compliance
Easy to set up and use
- Intuitive touchscreen with Setup Wizard
- Snap-on valve set
Flow-through connector that links ExactaMix valves to inlets and source containers. Custom design snaps easily onto the ExactaMix main module and features numbered ports and large-bore outlet connector for patient bag filling. Sterile, non-DEHP.
PVC tubing set with push-on connector on one end to attach to a valve set and a spike on the opposite end to attach a source container. Latex-free and non-DEHP. Available in large and small bore, with or without vent. Also available with Luer Lock end for use with syringes.
Empty ethylene vinyl acetate (EVA) bag used for sterile IV solutions. Includes filling port, injection port and administration port. Latex-free and non-DEHP. Available in various sizes.
Calibration bags plus various caps and connectors used in conjunction with other ExactaMix disposables.
For safe and proper use of the devices mentioned herein, refer to the appropriate Instructions for Use or Operator’s Manual.
EVA bags:
Riskin A et al. ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Standard versus individualized parenteral nutrition. Clin Nutr. 2018 Dec;37(6 Pt B):2409-2417.
Flynn EA et al. Observational study of accuracy in compounding i.v. admixtures atfive hospitals. Am J Health Syst Pharm. 1997;54: 904–912.
Kriz A et al. Cost-Consequences Analysis of Increased Utilization of Triple-Chamber-Bag Parenteral Nutrition in Preterm Neonates in Seven European Countries. Nutrients. 2020 Aug 20;12(9):2531.
Dickson LB et al. Automated compounder for adding ingredients to parenteral nutrient base solutions. Am J Hosp Pharm. 1993;50: 678–682.
MacKay MW et al. Pediatric parenteral nutrition via computerized worksheet and automated compounding. Nutrition in Clinical Practice. 2000;15(3):130-137
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