Taiwan FDA registration 3ba044fa0f1f03d6cec8119b3b354482
Alifa Hyalous Skin Filler
TW: 艾麗膚玻顏皮膚填補劑
Taiwan·Risk Class 3·Hekang Biotechnology Co., Ltd. Biomedical Products Factory·Registered May 21, 2014 – Apr 08, 2019CancelledRegistration details
- Analysis ID
- 3ba044fa0f1f03d6cec8119b3b354482
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ORIENT EUROPHARMA CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.0007 Hyaluronic acid implants
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- May 21, 2014
- Expiry Date
- Apr 08, 2019
- Cancellation Date
- Jun 22, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Alifa Hyalous Skin Filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3ba044fa0f1f03d6cec8119b3b354482 and manufactured by Hekang Biotechnology Co., Ltd. Biomedical Products Factory. The authorized representative in Taiwan is ORIENT EUROPHARMA CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices