Taiwan FDA registration dffa5df9932ae59ec423f4e618e6d374

Ti Star Internal Fixture System-Accessories

TW: 台灣之星內八角植體系統之配件

Taiwan·Risk Class 2·MD·T-PLUS IMPLANT TECH. CO., LTD.·Registered Dec 09, 2013 – Dec 09, 2018Cancelled

Registration details

Analysis ID: dffa5df9932ae59ec423f4e618e6d374
License Form: Ministry of Health Medical Device Manufacturing No. 004241

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): F3630 Dental bridges for bone explants
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Dec 09, 2013
Expiry Date: Dec 09, 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 Ti Star Internal Fixture System-Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dffa5df9932ae59ec423f4e618e6d374 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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