Taiwan FDA registration dac2019f7bd2f9ab0cab1cf1e93e31bf
"ANGELUS" Root Canal Post (Non-Sterile)
TW: "安吉樂" 根管中心柱釘 (未滅菌)
Registration details
- Analysis ID
- dac2019f7bd2f9ab0cab1cf1e93e31bf
- License Form
- Ministry of Health Medical Device Import No. 016667
- Customs Code
- DHA09401666700
Company information
- Manufacturer
- ANGELUS INDUSTRIA DE PRODUTOS ODONTOLOGICOS S/A
- Manufacturer Country
- Brazil
- Authorized Representative
- YOUNG SUN DEVELOP CO.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3810 tube center column nail
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 20, 2016
- Expiry Date
- Jun 20, 2021
About this record
Access comprehensive regulatory information for "ANGELUS" Root Canal Post (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dac2019f7bd2f9ab0cab1cf1e93e31bf and manufactured by ANGELUS INDUSTRIA DE PRODUTOS ODONTOLOGICOS S/A. The authorized representative in Taiwan is YOUNG SUN DEVELOP CO..
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