Taiwan FDA registration f1425a83c130b99cdc0e1f7e859e5a17
"Yi Ke Vi Wadent" Dental Hand Instruments (Unsterilized)
TW: "義獲嘉偉瓦登特" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·GEB. RENGGLI AG;;IVOCLAR VIVADENT AG·Registered Jul 19, 2018 – Jul 19, 2023CancelledRegistration details
- Analysis ID
- f1425a83c130b99cdc0e1f7e859e5a17
- Customs Code
- DHA09401933302
Company information
- Manufacturer
- GEB. RENGGLI AG;;IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein;;Switzerland
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jul 19, 2018
- Expiry Date
- Jul 19, 2023
- Cancellation Date
- Mar 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Yi Ke Vi Wadent" Dental Hand Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1425a83c130b99cdc0e1f7e859e5a17 and manufactured by GEB. RENGGLI AG;;IVOCLAR VIVADENT AG. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
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