Taiwan FDA registration e3ac8333c4a09ab3e10b0a6a96890769
“Prevest Denpro” MTA Plus Root & Pulp Treatment Material
TW: “培衛登普”緬體椰根管和牙髓治療材料
Taiwan·Risk Class 2·MD·Prevest Denpro Limited·Registered Sep 04, 2015 – Sep 04, 2020CancelledRegistration details
- Analysis ID
- e3ac8333c4a09ab3e10b0a6a96890769
- License Form
- Ministry of Health Medical Device Import No. 027660
- Customs Code
- DHA05602766003
Company information
- Manufacturer
- Prevest Denpro Limited
- Manufacturer Country
- India
- Authorized Representative
- WELCHANT DENTAL SUPPLY CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3820 Root canal filling resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 04, 2015
- Expiry Date
- Sep 04, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Prevest Denpro” MTA Plus Root & Pulp Treatment Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3ac8333c4a09ab3e10b0a6a96890769 and manufactured by Prevest Denpro Limited. The authorized representative in Taiwan is WELCHANT DENTAL SUPPLY CO., LTD..
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