Zhang Yu
Co-founder, General Manager and head of R&D and quality control. Mericonn’s profile states more than 20 years of R&D experience, with responsibility across company operations, product development and quality management.
Founded in Shenzhen in 2019, Mericonn brings medical-device R&D, production, quality control and export-market experience into one company.

Shenzhen Mericonn Technology Co., Ltd. was established in 2019 as a Class II home medical device manufacturer integrating research and development, production and sales. Its current portfolio spans respiratory care, prenatal monitoring, vital-sign monitoring and baby-care products.
The company positions itself around independent development and production, with a stated focus on premium, professional, reliable and easy-to-use products. That direction is reflected in a deliberately concentrated product range rather than an unrelated catalogue.
Mericonn’s official company profile describes a quality system reaching from R&D and supply chain control through production and finished-product inspection. It also states in-house injection molding, mesh nebulizer plate production, assembly and quality testing capabilities.
The company’s mission is to protect healthier beginnings and support the daily care that follows. For business partners, that means translating product reliability into clear specifications, controlled processes and evidence that can be checked at exact-model level.
Co-founder, General Manager and head of R&D and quality control. Mericonn’s profile states more than 20 years of R&D experience, with responsibility across company operations, product development and quality management.
Co-founder and Deputy General Manager. The company profile states nearly 20 years of medical-device export experience and more than 10 years of participation in product development.
Begin with the user and care routine, then decide what the product truly needs.
Keep claims connected to documents, models, indications and markets.
Strengthen product and quality fundamentals before chasing short-term scale.
Positioned around R&D and manufacturing of Class II home medical devices.
Domestic registration progress and FDA clearance for the named fetal Doppler series.
The company states ISO 9001 and ISO 13485 certification; current certificates remain subject to document review.
In-house injection molding, mesh plate production, assembly and quality testing described in the official profile.
FDA 510(k) clearance recorded for named mesh nebulizer models.