Taiwan FDA registration f876175f4f9c0222db99e4f06df1ea18
"DENTSPLY Professional" Dental hand instrument (Non-Sterile)
TW: "登士派" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·DENTSPLY PROFESSIONAL·Registered May 23, 2014 – May 23, 2019CancelledRegistration details
- Analysis ID
- f876175f4f9c0222db99e4f06df1ea18
- License Form
- Ministry of Health Medical Device Import No. 014162
- Customs Code
- DHA09401416202
Company information
- Manufacturer
- DENTSPLY PROFESSIONAL
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Branch of American Denspie Co., Ltd
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 23, 2014
- Expiry Date
- May 23, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "DENTSPLY Professional" Dental hand instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f876175f4f9c0222db99e4f06df1ea18 and manufactured by DENTSPLY PROFESSIONAL. The authorized representative in Taiwan is Taiwan Branch of American Denspie Co., Ltd.
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