Diagnostic System
Experience ACIST Pro™
The ACIST Pro™ System is a next-generation, variable-rate contrast management system designed for precise delivery of contrast media in interventional cardiology.
From an intuitive user interface to visual prompts that simplify troubleshooting and setup, ACIST Pro delivers enhancements to drive even more clinical and economic value.
The touchscreen is used to operate the system. A cable from the touchscreen connects to the processing unit. An optional bedrail mount for the touchscreen is also available.
There are two bottle holders; one holds the contrast bottle used during the procedure and one stores a second contrast bottle.
The syringe sleeve positions the syringe to ensure proper engagement with the motor-controlled actuator. The sleeve can be rotated to allow the syringe to be inserted and removed.
Secures the manifold in place during the procedure.
The air column sensor secures the patient tubing into place and detects an air column in the tubing.
Allows connection of the AngioTouch Hand Controller directly to the injector. Connection of the hand controller is required, either using these connectors or by connecting to the optional AngioTouch Module.
The weighted mallet is used to tap the fluid pathway and components to help dislodge and remove air.
The transducer cartridge holder couples the transducer cartridge to the system transducer diaphragm to read invasive blood pressure signals.
The saline pump delivers saline through the sterile fluid pathway, and is used to remove air and flush contrast from the patient tubing.
A visual on-screen enables the cath lab team to monitor and report dosing in relation to the target limit, without having to do it mentally.
Profiles facilitate customized procedure planning and setup; physicians can have customized presets based on their preferences and use cases.
On-screen troubleshooting simplifies setup
A visual on-screen enables the cath lab team to monitor and report dosing in relation to the target limit, without having to do it mentally.
Profiles facilitate customized procedure planning and setup; physicians can have customized presets based on their preferences and use cases.
On-screen troubleshooting simplifies setup
Key enhancements may provide value above and beyond what you have come to expect from your contrast delivery system.
Setup time is
33% faster
than CVi
Up to
30% reduction in CI-AKI
vs manual injection1
Up to
96% reduction
in clinician radiation exposure*2,3
Be among the first to know!
A visual on-screen enables the cath lab team to monitor and report dosing in relation to the target limit, without having to do it mentally.
Profiles facilitate customized procedure planning and setup; physicians can have customized presets based on their preferences and use cases.
On-screen troubleshooting simplifies setup
1. Call J, Sacrinty M, Applegate R, Little W, Santos R et al. (2006) 1. Automated contrast injection in contemporary practice during cardiac catheterization and PCI: effects on contrast-induced nephropathy. J Invasive Cardiol 18 (10): 469-474.; Minsinger KD, Kassis HM, Block CA, Sidhu M, Brown JR (2014) Meta-analysis of the effect of automated contrast injection devices versus manual injection and contrast volume on risk of contrast-induced nephropathy. Am J Cardiol 113 (1): 49-53.
2. NU-CLAIM-41
Important Safety Info:The ACIST ProTM Diagnostic System is designed to be used by a physician to inject contrast media and saline during angiography. It should be used with appropriateradiographic imaging and blood pressure monitoring and electrocardiogram. Additionally, standard equipment for cardiopulmonary resuscitation and drugs for the treatment of contrast media-induced drug reactions should be available. The ACIST Pro system must be operated by or be under the immediate and direct supervision of a physician trained in angiography and the operation of this unit. For maximum safety, use only material provided by ACIST Medical Systems in conjunction with ACIST Pro. Please refer to the Instructions for Use for more important safety information. Contamination of patient kits or the contrast container septum posesa risk of serious patient injury due to infection. If suspected contamination has occurred, replace the affected item.
An air embolism can cause patient injury or death. The operator must take care and follow a defined procedure consistent with the ACIST Pro Instructions for Use, are essential to avoid injecting air and causing an embolism. Before injections, clear all air from the entire patient kit and the angiographic catheter. It is necessary to reference the ACIST Pro Instructions for Use to review all important safety information relating to the device, and particularly to the prevention of air embolisms, as the ACIST Pro’s sensor systems are not designed to replace the vigilance and care required of the operator in preventing such events.
