Taiwan FDA registration 7fdf89205dbc4f9fd1d48223012545da
“Caulk” SDR Plus
TW: “寇克”思迪爾帕拉斯流動性樹脂補牙材
Taiwan·Risk Class 2·MD·DENTSPLY CAULK·Registered Sep 08, 2019 – Sep 08, 2024ExpiredRegistration details
- Analysis ID
- 7fdf89205dbc4f9fd1d48223012545da
- License Form
- Ministry of Health Medical Device Import No. 032836
- Customs Code
- DHA05603283608
Company information
- Manufacturer
- DENTSPLY CAULK
- Manufacturer Country
- United States
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 08, 2019
- Expiry Date
- Sep 08, 2024
About this record
Access comprehensive regulatory information for “Caulk” SDR Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fdf89205dbc4f9fd1d48223012545da and manufactured by DENTSPLY CAULK. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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