Taiwan FDA registration cae54006dc809ff3e22b5e147f10bf43
Juvederm Plumper (with Lidocaine)
TW: 喬雅登豐顏(含利多卡因)
Registration details
- Analysis ID
- cae54006dc809ff3e22b5e147f10bf43
- Customs Code
- DHA00602325701
Company information
- Manufacturer
- ALLERGAN
- Manufacturer Country
- France
- Authorized Representative
- ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND)
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
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Feb 15, 2012
- Expiry Date
- Feb 15, 2027
About this record
Access comprehensive regulatory information for Juvederm Plumper (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 cae54006dc809ff3e22b5e147f10bf43 and manufactured by ALLERGAN. The authorized representative in Taiwan is ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND).
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.
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