Taiwan FDA registration 6a4731412a26c03edb7d531980952d5d
EZ Plus Internal Fixture System
TW: 易智內三角植體系統
Taiwan·Risk Class 3·MD·T-PLUS IMPLANT TECH. CO., LTD.·Registered Aug 29, 2013 – Aug 29, 2028ActiveRegistration details
- Analysis ID
- 6a4731412a26c03edb7d531980952d5d
- License Form
- Ministry of Health Medical Device Manufacturing No. 004217
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
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 29, 2013
- Expiry Date
- Aug 29, 2028
About this record
Access comprehensive regulatory information for EZ Plus 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 6a4731412a26c03edb7d531980952d5d 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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