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Ti Star Internal Fixture System-Accessories - Taiwan Registration dffa5df9932ae59ec423f4e618e6d374

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..

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.

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dffa5df9932ae59ec423f4e618e6d374
Registration Details
Taiwan FDA Registration: dffa5df9932ae59ec423f4e618e6d374
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Device Details

Ti Star Internal Fixture System-Accessories
TW: ๅฐ็ฃไน‹ๆ˜Ÿๅ…งๅ…ซ่ง’ๆค้ซ”็ณป็ตฑไน‹้…ไปถ
Risk Class 2
MD
Cancelled

Registration Details

dffa5df9932ae59ec423f4e618e6d374

Ministry of Health Medical Device Manufacturing No. 004241

Company Information

Taiwan, Province of China

Product Details

F Dental devices

F3630 Dental bridges for bone explants

Produced in Taiwan, China

Dates and Status

Dec 09, 2013

Dec 09, 2018

Jul 15, 2022

Cancellation Information

Logged out

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