Taiwan FDA registration 4ac6ec4a16a795d368aa8de3144079f4
“PULPDENT” ACTIVA Bio ACTIVE-RESTORATIVE
TW: “波普登”玻璃離子補牙材
Taiwan·Risk Class 2·MD·PULPDENT CORPORATION·Registered May 01, 2019 – May 01, 2024ExpiredRegistration details
- Analysis ID
- 4ac6ec4a16a795d368aa8de3144079f4
- License Form
- Ministry of Health Medical Device Import No. 032532
- Customs Code
- DHA05603253201
Company information
- Manufacturer
- PULPDENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- FRANKFURT TECHNOLOGY CO., LTD.
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)
- F3275 Dental cement (Sminting)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 01, 2019
- Expiry Date
- May 01, 2024
About this record
Access comprehensive regulatory information for “PULPDENT” ACTIVA Bio ACTIVE-RESTORATIVE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ac6ec4a16a795d368aa8de3144079f4 and manufactured by PULPDENT CORPORATION. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..
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