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EZ Plus Internal Fixture System - Taiwan Registration 6a4731412a26c03edb7d531980952d5d

Access comprehensive regulatory information for EZ Plus 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 6a4731412a26c03edb7d531980952d5d 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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6a4731412a26c03edb7d531980952d5d
Registration Details
Taiwan FDA Registration: 6a4731412a26c03edb7d531980952d5d
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Device Details

EZ Plus Internal Fixture System
TW: ๆ˜“ๆ™บๅ…งไธ‰่ง’ๆค้ซ”็ณป็ตฑ
Risk Class 3
MD

Registration Details

6a4731412a26c03edb7d531980952d5d

Ministry of Health Medical Device Manufacturing No. 004217

Company Information

Taiwan, Province of China

Product Details

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

F Dental devices

F3640

Produced in Taiwan, China

Dates and Status

Aug 29, 2013

Aug 29, 2028