"Ruifeng" in vitro cosmetic repair supplement (prosthetic milk) (unsterilized)
Taiwan·Risk Class 1·The second factory of Jingyun Plastic Co., Ltd·Registered Jul 24, 2009 – Jul 24, 2024Cancelled- Analysis ID
- 3284bb663aa15e748462ba671df71eb2
- Manufacturer
- The second factory of Jingyun Plastic Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- REGENCY INTERNATIONAL MARKETING CORP.
- Intended Use
- Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3800 Repair supplement for cosmetic use in the body
- Import Information
- Domestic;; Contract manufacturing
- Registration Date
- Jul 24, 2009
- Expiry Date
- Jul 24, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Ruifeng" in vitro cosmetic repair supplement (prosthetic milk) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3284bb663aa15e748462ba671df71eb2 and manufactured by The second factory of Jingyun Plastic Co., Ltd. The authorized representative in Taiwan is REGENCY INTERNATIONAL MARKETING CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Ruifeng International Marketing Co., Ltd.;; Jingyun Plastic Co., Ltd. No. 2 Factory, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.