Taiwan FDA registration bd7b59921eb0a03d8ae8981c56ef5364
“angelus” Interlig Reinforcement
TW: “安喬拉斯”齒牙固定用補強材
Taiwan·Risk Class 2·MD·Angelus Indústria de Produtos Odontológicos S/A·Registered May 11, 2020 – May 11, 2025ExpiredRegistration details
- Analysis ID
- bd7b59921eb0a03d8ae8981c56ef5364
- License Form
- Ministry of Health Medical Device Import No. 033635
- Customs Code
- DHA05603363503
Company information
- Manufacturer
- Angelus Indústria de Produtos Odontológicos S/A
- Manufacturer Country
- Brazil
- Authorized Representative
- ASIANTOP ENTERPRISE 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)
- F3760 Denture re-liner re-reinding or replacement underlay resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 11, 2020
- Expiry Date
- May 11, 2025
About this record
Access comprehensive regulatory information for “angelus” Interlig Reinforcement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd7b59921eb0a03d8ae8981c56ef5364 and manufactured by Angelus Indústria de Produtos Odontológicos S/A. The authorized representative in Taiwan is ASIANTOP ENTERPRISE CO., LTD..
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