Taiwan FDA registration e587cf74387c41cb15f0681bfed2234c
"DORNIER" diode laser fiber
TW: “多尼爾”二極體雷射用光纖
Taiwan·Risk Class 2·Dornier MedTech America, Inc.·Registered Oct 27, 2009 – Oct 27, 2029ActiveRegistration details
- Analysis ID
- e587cf74387c41cb15f0681bfed2234c
- Customs Code
- DHA00602026702
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2009
- Expiry Date
- Oct 27, 2029
About this record
Access comprehensive regulatory information for "DORNIER" diode 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 e587cf74387c41cb15f0681bfed2234c and manufactured by Dornier MedTech America, Inc.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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