Taiwan FDA registration e16392daa271309fa7d02ca4a121be3f
"OVERFIBERS" Root canal post (Non-Sterile)
TW: "歐博士" 根管中心柱釘 (未滅菌)
Taiwan·Risk Class 1·MD·OVERFIBERS S.R.L.·Registered Sep 14, 2015 – Sep 14, 2020CancelledRegistration details
- Analysis ID
- e16392daa271309fa7d02ca4a121be3f
- License Form
- Ministry of Health Medical Device Import No. 015667
- Customs Code
- DHA09401566708
Company information
- Manufacturer
- OVERFIBERS S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- EUROTIDE TECHNOLOGY CO., LTD.
Product details
- 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
- Sep 14, 2015
- Expiry Date
- Sep 14, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "OVERFIBERS" 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 e16392daa271309fa7d02ca4a121be3f and manufactured by OVERFIBERS S.R.L.. The authorized representative in Taiwan is EUROTIDE TECHNOLOGY CO., LTD..
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