Taiwan FDA registration 3b8fa7829a3a15423434cb1415dd9fe0
“Dual Core” Dual-cured core build-up composite
TW: “帝卡”雙凝冠心建築樹脂
Taiwan·Risk Class 2·MD·VERICOM CO., LTD.·Registered Mar 31, 2017 – Mar 31, 2027ActiveRegistration details
- Analysis ID
- 3b8fa7829a3a15423434cb1415dd9fe0
- License Form
- Ministry of Health Medical Device Import No. 029620
- Customs Code
- DHA05602962001
Company information
- Manufacturer
- VERICOM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SUNDENT CORPORATION
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
- Mar 31, 2017
- Expiry Date
- Mar 31, 2027
About this record
Access comprehensive regulatory information for “Dual Core” Dual-cured core build-up composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b8fa7829a3a15423434cb1415dd9fe0 and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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