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“Dio” UF implant system-Angled abutment - Taiwan Registration a121e02481e5ea4bd5b0cd5acf56fb5e

Access comprehensive regulatory information for “Dio” UF implant system-Angled abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a121e02481e5ea4bd5b0cd5acf56fb5e and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

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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a121e02481e5ea4bd5b0cd5acf56fb5e
Registration Details
Taiwan FDA Registration: a121e02481e5ea4bd5b0cd5acf56fb5e
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Device Details

“Dio” UF implant system-Angled abutment
TW: “帝歐”悠福植體系統-角度式支台齒
Risk Class 2
MD

Registration Details

a121e02481e5ea4bd5b0cd5acf56fb5e

Ministry of Health Medical Device Import No. 030031

DHA05603003108

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3630 Dental bridges for bone explants

Imported from abroad

Dates and Status

Jul 27, 2017

Jul 27, 2027