Taiwan FDA registration c2e8c3348395805b9f98cc8329a23cb5
AnyOne Internal Fixture System
TW: 安萬內六角植體系統
Taiwan·Risk Class 3·MD·T-PLUS IMPLANT TECH. CO., LTD.·Registered Dec 13, 2013 – Dec 13, 2018CancelledRegistration details
- Analysis ID
- c2e8c3348395805b9f98cc8329a23cb5
- License Form
- Ministry of Health Medical Device Manufacturing No. 004243
Company information
- Manufacturer
- T-PLUS IMPLANT TECH. CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- T-PLUS IMPLANT TECH. CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 13, 2013
- Expiry Date
- Dec 13, 2018
- 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 AnyOne Internal Fixture System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c2e8c3348395805b9f98cc8329a23cb5 and manufactured by T-PLUS IMPLANT TECH. CO., LTD.. The authorized representative in Taiwan is T-PLUS IMPLANT TECH. CO., LTD..
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