Taiwan FDA registration 7e8b21cb5678fe1b44b762c79884c966
“Dornier” Thulio Performance Fiber
TW: “多尼爾”舒立歐效能光纖
Taiwan·Risk Class 2·MD·Dornier MedTech America, Inc.·Registered Jul 05, 2023 – Jul 05, 2028ActiveRegistration details
- Analysis ID
- 7e8b21cb5678fe1b44b762c79884c966
- License Form
- Ministry of Health Medical Device Import No. 036663
- Customs Code
- DHA05603666300
Company information
- Manufacturer
- Dornier MedTech America, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 05, 2023
- Expiry Date
- Jul 05, 2028
About this record
Access comprehensive regulatory information for “Dornier” Thulio Performance Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e8b21cb5678fe1b44b762c79884c966 and manufactured by Dornier MedTech America, Inc.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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