FuChia Consultant Co., Ltd.
Update：2026/11/10
Industries
Main Industry
Professional Services
Main Product/Service
1. Medical Device Regulatory Consulting Services: Specializing in medical device registration, quality system establishment, FDA and TFDA regulatory applications, as well as technical documentation planning for smart healthcare and Software as a Medical Device (SaMD).
2. Medical Device Import/Export and License Representation Services: Assisting domestic and foreign manufacturers in successfully completing product importation, regulatory applications, and market distribution operations.
2. Medical Device Import/Export and License Representation Services: Assisting domestic and foreign manufacturers in successfully completing product importation, regulatory applications, and market distribution operations.
The content above was translated by Ai
Founded Year
2019
Unified Business No.
50916422
Status
Active
Number of Employees
6
Total capital
5,000,000 (NT$)
Location of Company
Taiwan
, Taoyuan City
Company names, registration status, legal representatives, founding years, paid-in capital, registered addresses, and other details are sourced from business registration records maintained by Taiwan’s Administration of Commerce, Ministry of Economic Affairs. Exit status includes Emerging Stock Board listings, M&A, and IPOs. Information on overseas expansion is self-reported by startups.
Note 1: FINDIT compiles company information from public and other sources for reference and does not serve as a point of contact for the companies listed.
Note 2: Some company profiles and product/service descriptions are translated using AI and provided for reference only. In case of discrepancies or ambiguity, the original text prevails.
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About the Company
FuChia Consultant Co., Ltd. specializes in medical device regulatory and medical device quality system consulting services, assisting domestic and foreign medical device manufacturers to successfully enter the Taiwan, US, and international markets. The company provides professional regulatory services for TFDA, FDA, ISO 13485, SaMD, and AI medical devices, covering assistance to clients in product classification determination applications, registration and approval, QMS establishment, technical documentation writing, and international regulatory strategy planning. Leveraging rich practical experience and Chinese-English technical documentation capabilities, FuChia Consultant is committed to helping clients improve regulatory efficiency, reduce market entry risks, and accelerate the successful market launch of medical device products.
The content above was translated by Ai
