It can be easier to make sure you get the most out of your medical equipment if you have the appropriate user manual for an agilia infusion pump. When your pump has a problem and you need to know how to fix it, having a guide can assist you know what to do. You can keep track of all your infusions with the aid of a guidebook. Knowing what to do in the event that you have to re-start an infusion from scratch can be useful.
Besides its ease of use, Volumat MC Agilia volumetric infusion pump user manual has a built-in security system to prevent the risk of free flow. It also has a pressure monitoring system to prevent the risk of under-infusion of medications.
Volumat MC Agilia volumetric infusion pump has an internal battery to ensure a minimum autonomy of 8 hours when 125 ml/h is in use. The device is also designed to operate during mains power cut. In order to achieve optimal performance, Fresenius-Vial recommends the presence of qualified personnel in the establishment. The pump uses a Link system for communication with the communications system.
Volumat MC Agilia volumetric infusion pump is programmed in three modes. It has an automatic occlusion checking system that prevents the risk of free-flow. It also has an infusion monitoring system. It is a portable device designed for use in multiple hospital care areas.
During the infusion process, the Injectomat agilia syringe pump will display a variety of symbols to notify the user of the status of the infusion. These symbols are usually associated with a single event, such as a pause, bolus or increment rule. The following is a brief description of these symbols and the functions they perform.
The data set symbol (DSM) is a small symbol located on the pump's display screen. It functions as an indicator of the active data set, as well as showing the syringe used in the infusion. In addition to the syringe symbol, there are also the data set symbols for bolus volume, duration and dose.
The syringe symbol is the same as the on-pump syringe symbol. This symbol displays information on the on-pump syringe, including the syringe used in the procedure, its time of manufacture, and its date of manufacture.
According to reports, the FDA has issued a class one (if class one is even possible) recall for the Volumat MC Agilia pump infusion System. The Volumat is intended for use in hospitals, ambulatory care centers, and pediatric clinics and can be used in a number of treatment settings. Fluids are to be administered intravenously using the technique. It is portable, portable, and compact. It is produced by the Lake Zurich, Illinois-based corporation Fresenius Kabi. Infusion pumps are one of its more well-known devices.
According to the company's website, complaints concerning its Volumat MC Agilia Infusion System number fourteen in total. The corporation sent out an urgent device recall letter on June 21 but has not specified a specific cause for the recall. The business listed a number of specific steps it intended to take in the letter to reduce the risk to patients.
Several software errors are at play in the Fresenius Kabi USA Volumat MC Agilia Infusion System and Vigilant Drug'Lib. These errors could have serious consequences, including the potential to cause under-infusion and over-infusion of medication, resulting in serious injury and even death.
Fresenius Kabi has received 14 complaints related to these errors. The company subsequently recalled the Volumat MC Agilia iv infusion pump and Vigilant Drug'Lib. The company also issued a related letter containing several specific actions it took to help prevent patient harm.
Fresenius Kabi is a global health care company specializing in medicines, transfusion, clinical nutrition and technologies for infusion. It is also part of the Center for Veterinary Medicine (FDA-CVM) which is a part of the U.S. Food and Drug Administration (FDA).
The Vigilant Drug'Lib is a dose error reduction software application. It allows pharmacists to configure drug doses and limits. It also helps to identify dose errors, and can be customized to meet clinical needs.
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Thousands of Volumat MC agilia infusion pumps are being recalled in the U.S. by Fresenius Kabi. The device's "Keep Vein Open" alarm signal is causing problems for some users. The company is updating its software library to correct issues, and users should follow specific instructions to prevent harm.
Fresenius Kabi has received 14 complaints about the device. The company identified four software errors that could lead to serious patient harm. It will upgrade its KVO alarm signal to high priority. This means that a clinician would be notified when the infusion completes. It is important to respond to the alarm as soon as possible. Failure to respond could lead to under-infusion or delay in care.
The Volumat MC Agilia infusion pump is used in several hospital facilities. It is designed to administer fluids in pediatrics and neonates. It also is used to administer fluids in adults. It is a small, portable infusion pump.