Taiwan FDA registration 2f0c9b05e7210fe4648c6810feee4ff3
“Caulk” Aquasil Ultra Plus Impression Material
TW: “寇克”新水精靈超印模材
Taiwan·Risk Class 2·MD·DENTSPLY CAULK·Registered Oct 14, 2019 – Oct 14, 2024ExpiredRegistration details
- Analysis ID
- 2f0c9b05e7210fe4648c6810feee4ff3
- License Form
- Ministry of Health Medical Device Import No. 032867
- Customs Code
- DHA05603286706
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)
- F3660 impression material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 14, 2019
- Expiry Date
- Oct 14, 2024
About this record
Access comprehensive regulatory information for “Caulk” Aquasil Ultra Plus Impression Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f0c9b05e7210fe4648c6810feee4ff3 and manufactured by DENTSPLY CAULK. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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