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ST Internal Fixture System - Taiwan Registration c9e8e1cd99d23cb2812623e6f31c24eb

Access comprehensive regulatory information for ST 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 c9e8e1cd99d23cb2812623e6f31c24eb 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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c9e8e1cd99d23cb2812623e6f31c24eb
Registration Details
Taiwan FDA Registration: c9e8e1cd99d23cb2812623e6f31c24eb
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Device Details

ST Internal Fixture System
TW: ็พŽไฝณๅขƒๅ…งๅ…ญ่ง’ๆค้ซ”็ณป็ตฑ
Risk Class 3
MD

Registration Details

c9e8e1cd99d23cb2812623e6f31c24eb

Ministry of Health Medical Device Manufacturing No. 004694

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3640 Bone explants

Produced in Taiwan, China

Dates and Status

Nov 04, 2014

Nov 04, 2024