Taiwan FDA registration 01749bbda5c92c3a6279953cd45d807b
"Hon Hai" root tube paper needle (unsterilized)
TW: “鴻海”根管紙針(未滅菌)
Taiwan·Risk Class 1·TIANJIN GAPADENT CO., LTD·Registered Aug 21, 2018 – Aug 21, 2023ExpiredRegistration details
- Analysis ID
- 01749bbda5c92c3a6279953cd45d807b
- Customs Code
- DHA09600352807
Company information
- Manufacturer
- TIANJIN GAPADENT CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- HONHI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3830 Root Canal
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 21, 2018
- Expiry Date
- Aug 21, 2023
About this record
Access comprehensive regulatory information for "Hon Hai" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 01749bbda5c92c3a6279953cd45d807b and manufactured by TIANJIN GAPADENT CO., LTD. The authorized representative in Taiwan is HONHI MEDICAL CO., LTD..
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