Taiwan FDA registration 912c6bbbe88a93f4c766816f34427bd3
"Densberg Tianjin Factory" root tube paper needle (sterilization)
TW: "登士柏 天津廠" 根管紙針(滅菌)
Taiwan·Risk Class 1·Dentsply Dental (TianJin) Co., Ltd.·Registered Apr 23, 2019 – Apr 23, 2029ActiveRegistration details
- Analysis ID
- 912c6bbbe88a93f4c766816f34427bd3
- Customs Code
- DHA09600376304
Company information
- Manufacturer
- Dentsply Dental (TianJin) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Root Canal Paper Needle (F.3830)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3830 Root Canal
- Import Information
- QMS/QSD;; Chinese goods;; input
Dates and status
- Registration Date
- Apr 23, 2019
- Expiry Date
- Apr 23, 2029
About this record
Access comprehensive regulatory information for "Densberg Tianjin Factory" root tube paper needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 912c6bbbe88a93f4c766816f34427bd3 and manufactured by Dentsply Dental (TianJin) Co., Ltd.. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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