Taiwan FDA registration ec8b4b6bab1ab0a7b35de4e89f182a45
FACILLE Light Facial Dermal Implant
TW: 法思麗輕感皮下填補劑
Taiwan·Risk Class 3·MD·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered Jun 29, 2021 – Nov 16, 2028ActiveRegistration details
- Analysis ID
- ec8b4b6bab1ab0a7b35de4e89f182a45
- License Form
- Ministry of Health Medical Device Manufacturing No. 004837
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SCIVISION BIOTECH INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I0007 Hyaluronic acid implants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 29, 2021
- Expiry Date
- Nov 16, 2028
About this record
Access comprehensive regulatory information for FACILLE Light Facial Dermal Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ec8b4b6bab1ab0a7b35de4e89f182a45 and manufactured by Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory. The authorized representative in Taiwan is SCIVISION BIOTECH INC..
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