301371SZSE
🚨 Material Event

Announcement on Acceptance of Medical Device Registration Certificate Application

Harbin Fuerjia Technology Co., Ltd.··2 pages

✨ AI Summary

Harbin Furenjia Technology Co., Ltd. announced that its medical device product, recombinant humanized collagen type III freeze-dried fiber, has been accepted for registration by the National Medical Products Administration. This marks a significant step towards market entry for their first shallow injection filler product, aiming to expand their presence in the medical aesthetics market.

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Full Translation

AI Translation· gemini_document

Securities Code: 301371

Securities Abbreviation: Furenjia

Announcement Number: 2026-033

Harbin Furenjia Technology Co., Ltd.

Announcement on Acceptance of Medical Device Registration Certificate Application

The Company and all members of the Board of Directors guarantee that the information disclosed is true, accurate, and complete, and that there are no false records, misleading statements, or major omissions.

Harbin Furenjia Technology Co., Ltd. (hereinafter referred to as the "Company") announced on February 24, 2026, the "Announcement on the Completion of Clinical Trials for Class III Medical Device Products" (Announcement Number: 2026-002). The Company's research and development product, "Recombinant Humanized Collagen Type III Freeze-Dried Fiber," has completed clinical trials and obtained a clinical trial summary report, enabling the submission of registration application materials.

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