Taiwan FDA registration 5192151c7bbef15a473ae225f6aecaa6
“KURARAY NORITAKE” CLEARFIL DC CORE PLUS
TW: “可樂麗則武”克立菲爾雙聚式冠心堆築黏合劑
Taiwan·Risk Class 2·MD·Kuraray Noritake Dental Inc. Niigata plant·Registered Apr 13, 2018 – Apr 13, 2028ActiveRegistration details
- Analysis ID
- 5192151c7bbef15a473ae225f6aecaa6
- License Form
- Ministry of Health Medical Device Import No. 031032
- Customs Code
- DHA05603103202
Company information
- Manufacturer
- Kuraray Noritake Dental Inc. Niigata plant
- Manufacturer Country
- Japan
- Authorized Representative
- JOYO WELLDENT 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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 13, 2018
- Expiry Date
- Apr 13, 2028
About this record
Access comprehensive regulatory information for “KURARAY NORITAKE” CLEARFIL DC CORE PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5192151c7bbef15a473ae225f6aecaa6 and manufactured by Kuraray Noritake Dental Inc. Niigata plant. The authorized representative in Taiwan is JOYO WELLDENT CO., LTD..
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