Taiwan FDA registration c9e8e1cd99d23cb2812623e6f31c24eb
ST Internal Fixture System
TW: 美佳境內六角植體系統
Registration details
- Analysis ID
- c9e8e1cd99d23cb2812623e6f31c24eb
- License Form
- Ministry of Health Medical Device Manufacturing No. 004694
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 Bone explants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 04, 2014
- Expiry Date
- Nov 04, 2024
About this record
Access comprehensive regulatory information for ST 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 c9e8e1cd99d23cb2812623e6f31c24eb 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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