Taiwan FDA registration df8cb4bbd27606258d85b804a7a1026a
“Spacer” Light-curing temporary filling material
TW: “斯必特”暫時性填補牙材
Taiwan·Risk Class 2·MD·VERICOM CO., LTD.·Registered Sep 07, 2018 – Sep 07, 2028ActiveRegistration details
- Analysis ID
- df8cb4bbd27606258d85b804a7a1026a
- License Form
- Ministry of Health Medical Device Import No. 031595
- Customs Code
- DHA05603159507
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
- Sep 07, 2018
- Expiry Date
- Sep 07, 2028
About this record
Access comprehensive regulatory information for “Spacer” Light-curing temporary filling material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df8cb4bbd27606258d85b804a7a1026a and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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