Taiwan FDA registration 286e1061ee85c08601b28ce3c0ad2304
“KURARAY NORITAKE” CLEARFIL AP-X Esthetics Flow
TW: “可樂麗則武”克立菲爾光聚合流動型複合樹脂
Taiwan·Risk Class 2·MD·Kuraray Noritake Dental Inc. Niigata plant·Registered Mar 31, 2018 – Mar 31, 2028ActiveRegistration details
- Analysis ID
- 286e1061ee85c08601b28ce3c0ad2304
- License Form
- Ministry of Health Medical Device Import No. 031011
- Customs Code
- DHA05603101107
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
- Mar 31, 2018
- Expiry Date
- Mar 31, 2028
About this record
Access comprehensive regulatory information for “KURARAY NORITAKE” CLEARFIL AP-X Esthetics Flow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 286e1061ee85c08601b28ce3c0ad2304 and manufactured by Kuraray Noritake Dental Inc. Niigata plant. The authorized representative in Taiwan is JOYO WELLDENT CO., LTD..
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