Taiwan FDA registration f15b0a9b9c6fdedb6fe1ffecab2d71ce
"Professional" Dental hand instrument (Non-sterile)
TW: "普菲納" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·DENTSPLY PROFESSIONAL·Registered Sep 20, 2017 – Sep 20, 2027ActiveRegistration details
- Analysis ID
- f15b0a9b9c6fdedb6fe1ffecab2d71ce
- License Form
- Ministry of Health Medical Device Import No. 018333
- Customs Code
- DHA09401833307
Company information
- Manufacturer
- DENTSPLY PROFESSIONAL
- Manufacturer Country
- United States
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 20, 2017
- Expiry Date
- Sep 20, 2027
About this record
Access comprehensive regulatory information for "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 f15b0a9b9c6fdedb6fe1ffecab2d71ce and manufactured by DENTSPLY PROFESSIONAL. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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