Taiwan FDA registration c28354b1e41ecca5af93fba2793dedda
"Bio-Art" Prophy Powder (Non-Sterile)
TW: "百歐爾" 口腔研磨磨光粉 (未滅菌)
Registration details
- Analysis ID
- c28354b1e41ecca5af93fba2793dedda
- License Form
- Ministry of Health Medical Device Import No. 016457
- Customs Code
- DHA09401645702
Company information
- Manufacturer
- BIO-ART EQUIPAMENTOS ODONTOLOGICOS LTDA.
- Manufacturer Country
- Brazil
- Authorized Representative
- MNM BIOTECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first level recognition range of oral grinding polishing agent (F.6030) of the management measures for medical equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6030 Oral grinding polishing agent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 26, 2016
- Expiry Date
- Apr 26, 2026
About this record
Access comprehensive regulatory information for "Bio-Art" Prophy Powder (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 c28354b1e41ecca5af93fba2793dedda and manufactured by BIO-ART EQUIPAMENTOS ODONTOLOGICOS LTDA.. The authorized representative in Taiwan is MNM BIOTECHNOLOGY CO., LTD.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices