Taiwan FDA registration c76fca0c64475e42241c9c9f81578a4f
Aliva dermal filler
TW: 艾麗膚真皮填補劑
Taiwan·Risk Class 3·Hekang Biotechnology Co., Ltd. Biomedical Products Factory·Registered Oct 02, 2013 – Apr 25, 2018CancelledRegistration details
- Analysis ID
- c76fca0c64475e42241c9c9f81578a4f
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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Oct 02, 2013
- Expiry Date
- Apr 25, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Aliva dermal filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c76fca0c64475e42241c9c9f81578a4f and manufactured by Hekang Biotechnology Co., Ltd. Biomedical Products Factory. The authorized representative in Taiwan is ORIENT EUROPHARMA CO., LTD..
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