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About us

  Beijing Hanson Born Medical Technology Co., Lid Medical Technology Co., Lid (Hengxin Medical for short), as an affliated company of WECAN MEDICINE GROUP LTD and established in 2009, is specialized in registration and consultancy services for NMPA ( CFDA ) medical products. As engaged in NMPA ( CFDA) registration and consultancy since 2002, its founder in one of professional consultants who firstly involved in NMPA ( CFDA ) registration in China. Hengxin Medical is abundant in excellent registration talents and third-party resources. Up to 70 talented people is enrolled into its core technical team, with 25% of graduate degree and 70% of bachelor degree, background covers general medicine, pharmacy, biological engineering, clinical examination, biomedical engineering biology and electromechanical. All have more than 3 years of experience in various fields. 

  Hengxin Medical always perform a systematic and hierarchical management and provide a service which is under strict QC procedures to ensure all projects can be integrated effectively and move forward. Customer services are in charge of project managers in cooperation with CTO. In this way, the customer demands will obtain effective feedback and we can adjust quickly, which result in a satisfied communication and an avoidance of project interrupted due to sudden events. Forging ahead and with adherence to original intention, we dedicate to provide high-quality and professional services for medical companies around world.

  We are professional because we are focused. ——All our efforts are made for you.

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Historical Cases

News Update

• Hengxin Medical has obtained the double certification of quality systemHengxin Medical has obtained the double certification of quality system
• You can trust our companyYou can trust our company
• New business partnersNew business partners
• Team building activitiesTeam building activities
• Company brochureCompany brochure
• International Business developmentInternational Business development
• *Regulations on supervision and administration of Medical Devices**Regulations on supervision and administration of Medical Devices*
• *Measures for the administration of registration and filing of medical devices*Measures for the administration of registration and filing of medical devices
• *Circular of the State Food and Drug Administration on Guidelines for Preparation of Technical Requirements for Medical Device Products (No. 8 of 2022) *Circular of the State Food and Drug Administration on Guidelines for Preparation of Technical Requirements for Medical Device Products (No. 8 of 2022)

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