Taiwan FDA registration e333a2a58c862a12117cef147fd2f1ed
“DenFil N” Light-cured restorative nano hybrid composite resin
TW: “登飛奈米”光聚合複合樹脂
Taiwan·Risk Class 2·MD·VERICOM CO., LTD.·Registered Mar 15, 2018 – Mar 15, 2028ActiveRegistration details
- Analysis ID
- e333a2a58c862a12117cef147fd2f1ed
- License Form
- Ministry of Health Medical Device Import No. 030968
- Customs Code
- DHA05603096802
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 15, 2018
- Expiry Date
- Mar 15, 2028
About this record
Access comprehensive regulatory information for “DenFil N” Light-cured restorative nano hybrid composite resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e333a2a58c862a12117cef147fd2f1ed and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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