Taiwan FDA registration 6098250030fea0531e438ab057275706
“Dornier” Holmium Laser Fiber
TW: “多尼爾”鈥雷射光纖
Taiwan·Risk Class 2·MD·Dornier MedTech America, Inc.·Registered Aug 27, 2019 – Aug 27, 2024ExpiredRegistration details
- Analysis ID
- 6098250030fea0531e438ab057275706
- License Form
- Ministry of Health Medical Device Import No. 032767
- Customs Code
- DHA05603276702
Company information
- Manufacturer
- Dornier MedTech America, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDEN INTERNATIONAL INC.
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)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 27, 2019
- Expiry Date
- Aug 27, 2024
About this record
Access comprehensive regulatory information for “Dornier” Holmium Laser Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6098250030fea0531e438ab057275706 and manufactured by Dornier MedTech America, Inc.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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