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2026.05.21
Dong-A ST and MEZOO Surge with Fivefold Growth in Q1, Chasing Daewoong Pharmaceutical and Seers Technology

 

While Daewoong Pharmaceutical and Seers Technology are making waves in Korea’s AI-powered hospital bed monitoring solution market, competitors Dong-A ST and MEZOO are drawing attention by rapidly expanding their market share in pursuit.

 

According to industry sources on the 20th, Dong-A ST has been rapidly increasing hospital deployments with “HiCardi,” an AI-based remote patient monitoring solution developed by Korean company MEZOO.

 

According to Dong-A ST, annual sales last year totaled 1,837 units, but the company sold 2,869 units in the first quarter of this year alone, surpassing last year’s total annual sales within a single quarter. This represents a 390.5% increase compared to the same period last year.

 

A Dong-A ST official stated, “We are accelerating our sales efforts with the goal of selling 10,000 units this year,” adding, “The solution has been receiving positive responses from both medical staff and patients.”

 

MEZOO provides a mobile remote patient monitoring solution capable of measuring and analyzing patients’ vital signs in real time. Since signing an exclusive distribution agreement with Dong-A ST, the company has rapidly expanded supply to domestic medical institutions. Its core products include the “HiCardi” series of patch-type patient monitoring devices and the “Live Studio” patient monitoring software platform. The company has adopted a subscription-based revenue model to reduce the initial implementation burden for healthcare institutions.

 

HiCardi is a patch-type wearable device attached to a patient’s body. It remotely monitors electrocardiogram (ECG), heart rate, arrhythmia, respiration, and fall detection in real time. Live Studio enables medical staff to simultaneously monitor patient conditions through dashboards and smartphones.



source : https://www.etnews.com/20260520000288

 

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하이카디® 시스템은 인허가에 따라 신생아, 소아, 청소년, 18세 이상 환자의 ECG 데이터를 측정하여 부정맥을 진단하는 의료기기로서 의료전문가가 사용하도록 설계되었습니다. 한국 KFDA로부터 의료기기 2등급 인증을 받았습니다. 유럽의료기기 지침(2007/47/EC에 따라 개정된 MDD 93/42/EEC)에 따라 준수된 Class IIb (CE2265). 의료기기 제품으로 CE 승인되었습니다. 미국 FDA는 Class II 510K로 승인 완료 예정입니다.

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