The core function and role of infusion pumps is to deliver medicines and nutrients in real-time, quantitatively, accurately, and precisely to save the lives of critically ill patients, overcome diseases, and grow and develop extremely low birth weight infants. In addition, the safety of the device's S/W and H/W is the life of the infusion pump and determines the success or failure of the market.

Due to the limitations of the original technology of existing pumps, doctors and nurses often witness medical accidents in which patients are in a critical situation due to inaccurate injection in real time, device problems, syringe defects, start up delay, etc.

In particular, very low birth weight infants, premature babies, and newborns require real-time, precise, and accurate infusion of medications and nutrients, which is key to their growth, development, and health, but this is not possible with conventional pumps, leaving medical staff with the task of checking and managing them, causing them to be overworked and stressed by unexplained medical errors and high turnover rates.

Until now, we have mainly demoed and verified the efficacy and safety in the NICU using a single pump, with very positive results, but this is the first time that the two hospitals have demoed it in the ER (Emergency Room), where multiple pumps are used and various situations are premised, and in the anesthesiology department and inpatient rooms, where accurate and precise infusion is key.

In the ICU, anesthesiology department, ER, and wards, CylinderPump was verified as a drug infusion pump that completely overcame the clinical effectiveness problems of existing pumps, and received very positive reviews, relieving the heavy workload inevitable with existing pumps and the intense stress of providing emergency treatment to patients in critical situations without knowing the cause.

Perfect clinical usability and solved the structural problem of syringe pumps that cannot visually check the real-time infusion status and situation Medical staff actively recommended it to other departments and requested publicity through conferences.

The Anyfusion cylinder pump was designated by the FDA as a high-level direct review breakthrough medical device as an alternative to overcome the clinical usability problems of the existing pump, and as a result, the existing pump will be replaced by a cylinder pump that is inappropriate for infusion pumps, which will be a game changer.

We will address the following points and focus on active marketing and rapid activation of the market in developed countries such as the United States, Japan, and Germany.

In intensive care units that use multiple pumps rather than NICUs that use a single pump, the air alarm (H/W problem), which has increased in proportion to the number of medicines injected, and the S/W error (S/W problem) caused by operation due to the user's inaccurate cognitive state due to short training, were requested as solutions.

The first is to fix and secure it in R&D department, and the second is to apply it to the development of the next product to become the perfect Anyfusion cylinder pump, and to synergize with the game changer by rapid paradigm shift in the global drug infusion pump market.

Thank you.