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AnyRidge Internal Fixture System - Taiwan Registration 20f990da85ca8a581663c92f4e0e7714

Access comprehensive regulatory information for AnyRidge 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 20f990da85ca8a581663c92f4e0e7714 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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20f990da85ca8a581663c92f4e0e7714
Registration Details
Taiwan FDA Registration: 20f990da85ca8a581663c92f4e0e7714
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Device Details

AnyRidge Internal Fixture System
TW: ๅฎ‰็‘žๆ™บๅ…งๅ…ญ่ง’ๆค้ซ”็ณป็ตฑ
Risk Class 3
MD
Cancelled

Registration Details

20f990da85ca8a581663c92f4e0e7714

Ministry of Health Medical Device Manufacturing No. 004244

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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