Taiwan FDA registration 1f813d01e42a5e1ebbe609547ef94976
“Allergan” Juvederm VOLIFT with Lidocaine
TW: “愛力根”喬雅登豐麗緹(含利多卡因)
Taiwan·Risk Class 3·MD·ALLERGAN·Registered Mar 29, 2016 – Mar 29, 2026ExpiredRegistration details
- Analysis ID
- 1f813d01e42a5e1ebbe609547ef94976
- License Form
- Ministry of Health Medical Device Import No. 027780
- Customs Code
- DHA05602778000
Company information
- Manufacturer
- ALLERGAN
- Manufacturer Country
- France
- Authorized Representative
- ALLERGAN PHARMACEUTICALS TAIWAN CO., LTD.
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
- Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and status
- Registration Date
- Mar 29, 2016
- Expiry Date
- Mar 29, 2026
About this record
Access comprehensive regulatory information for “Allergan” Juvederm VOLIFT with Lidocaine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1f813d01e42a5e1ebbe609547ef94976 and manufactured by ALLERGAN. The authorized representative in Taiwan is ALLERGAN PHARMACEUTICALS TAIWAN CO., LTD..
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