Taiwan FDA registration f02af52adcf5af9b68f6df2a5d06276e

"T-Plus" Surgical Guide (Non-Sterile)

TW: "美佳境" 手術導板 (未滅菌)

Taiwan·Risk Class 1·MD·T-PLUS IMPLANT TECH. CO., LTD.·Registered Apr 12, 2017 – Apr 12, 2022Cancelled

Registration details

Analysis ID: f02af52adcf5af9b68f6df2a5d06276e
License Form: Ministry of Health Medical Device Manufacturing No. 006684

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): F3980 Dental Intraosseous Implant Attachment
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 12, 2017
Expiry Date: Apr 12, 2022
Cancellation Date: Aug 03, 2020

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "T-Plus" Surgical Guide (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 f02af52adcf5af9b68f6df2a5d06276e and manufactured by T-PLUS IMPLANT TECH. CO., LTD.. The authorized representative in Taiwan is T-PLUS IMPLANT TECH. CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.