Taiwan FDA registration d96cd51d8aba81df018c7851ab1a5589
"Oufabo" glass fiber root column (indestructible)
TW: "歐法博" 玻璃纖維牙根柱(未滅菌)
Registration details
- Analysis ID
- d96cd51d8aba81df018c7851ab1a5589
- Customs Code
- DHA09402327309
Company information
- Manufacturer
- OVERFIBERS S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- EUROTIDE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Root Canal Center Pillar (F.3810)" of the Classification and Grading Management Measures for Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3810 Root canal center post
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 12, 2023
- Expiry Date
- Oct 12, 2028
About this record
Access comprehensive regulatory information for "Oufabo" glass fiber root column (indestructible) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d96cd51d8aba81df018c7851ab1a5589 and manufactured by OVERFIBERS S.R.L.. The authorized representative in Taiwan is EUROTIDE TECHNOLOGY 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