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2026.02.02
Park Jung-hwan, CEO of Mezoo: “This year is the decisive year for aRPM… confident in our competitive edge in top-tier hospitals”

Confidence in “HiCardi” and “HiCardi Plus” amid the full-scale intensification of competition among tertiary hospitals this year

Nurturing the next-generation product “HiCardi M350” as a key lever to widen the technology gap in overseas markets

박정환 메쥬 대표가 강원도 원주시 소재 회사 R&D센터에서 진행한 인터뷰에서 하이카디 솔루션에 대해 설명하고 있다. /사진=메쥬
Park Jung-hwan, CEO of Mezoo, explains the HiCardi solution during an interview conducted at the company’s R&D center in Wonju, Gangwon Province. / Photo = Mezoo

“This year, when competition centered on tertiary hospitals intensifies in earnest, I am confident that Mezoo’s solutions—designed from the outset for large hospitals—will prove their competitiveness,” said Park Jung-hwan, CEO of Mezoo.


Mezoo, an ambulatory Remote Patient Monitoring (aRPM) company, is entering a phase of full-scale market competition following its IPO preparations. On the 20th, Mezoo filed its securities registration statement and initiated the public offering process for its KOSDAQ listing.


Mezoo’s strategy is to elevate its position in the aRPM market by demonstrating the competitiveness of solutions tailored to the needs of advanced hospitals, while accelerating next-generation product development and overseas market expansion. The company’s core focus is aRPM technology that enables continuous measurement and transmission of vital signs even in environments where patients are mobile rather than confined to beds. Its key products are the wearable patch-based “HiCardi” and “HiCardi Plus.” These solutions collect ECG-centered biometric signals in real time and transmit them to hospital servers or the cloud, allowing medical staff to monitor multiple patients simultaneously on a single screen. Leveraging these strengths, Mezoo achieved cumulative sales of KRW 5.3 billion as of the third quarter of last year, surpassing its total revenue for the previous year (KRW 2.4 billion) and demonstrating strong growth momentum.


source : https://www.mt.co.kr/thebio/2026/02/02/2026013014362892456
 

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의료기기

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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