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AnyOne Internal Fixture System - Taiwan Registration c2e8c3348395805b9f98cc8329a23cb5

Access comprehensive regulatory information for AnyOne 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 c2e8c3348395805b9f98cc8329a23cb5 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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c2e8c3348395805b9f98cc8329a23cb5
Registration Details
Taiwan FDA Registration: c2e8c3348395805b9f98cc8329a23cb5
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Device Details

AnyOne Internal Fixture System
TW: ๅฎ‰่ฌๅ…งๅ…ญ่ง’ๆค้ซ”็ณป็ตฑ
Risk Class 3
MD
Cancelled

Registration Details

c2e8c3348395805b9f98cc8329a23cb5

Ministry of Health Medical Device Manufacturing No. 004243

Company Information

Taiwan, Province of China

Product Details

F Dental devices

F3640 Bone explants

Produced in Taiwan, China

Dates and Status

Dec 13, 2013

Dec 13, 2018

Jul 15, 2022

Cancellation Information

Logged out

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