Taiwan FDA registration 3939ac5a8a218c6e8dd5e1f8c3e1a082
“Mectron” Piezosurgery Bone Surgery Unit and Accessories
TW: “麥克龍”皮耶牙科超音波骨切割器及其配件
Taiwan·Risk Class 2·MD·MECTRON S.P.A.·Registered Jul 19, 2017 – Jul 19, 2027ActiveRegistration details
- Analysis ID
- 3939ac5a8a218c6e8dd5e1f8c3e1a082
- License Form
- Ministry of Health Medical Device Import No. 029948
- Customs Code
- DHA05602994809
Company information
- Manufacturer
- MECTRON S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- SUNDENT CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4120 bone cutters and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 19, 2017
- Expiry Date
- Jul 19, 2027
About this record
Access comprehensive regulatory information for “Mectron” Piezosurgery Bone Surgery Unit and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3939ac5a8a218c6e8dd5e1f8c3e1a082 and manufactured by MECTRON S.P.A.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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