Taiwan FDA registration 208f366ecd150adf2f806317c82ea65f
RADIESSE Lidocaine Injectable Implant
TW: 瑞得喜植入劑(含利多卡因)
Taiwan·Risk Class 3·MD·Merz North America, Inc.·Registered Oct 15, 2019 – Oct 15, 2024ExpiredRegistration details
- Analysis ID
- 208f366ecd150adf2f806317c82ea65f
- License Form
- Ministry of Health Medical Device Import No. 032974
- Customs Code
- DHA05603297407
Company information
- Manufacturer
- Merz North America, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE)
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)
- I9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 15, 2019
- Expiry Date
- Oct 15, 2024
About this record
Access comprehensive regulatory information for RADIESSE Lidocaine Injectable Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 208f366ecd150adf2f806317c82ea65f and manufactured by Merz North America, Inc.. The authorized representative in Taiwan is MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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