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“Dio” UF(II) Narrow Angled abutment - Taiwan Registration 232f4ae762b1b7ef4e34442d1ad33391

Access comprehensive regulatory information for “Dio” UF(II) Narrow 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 232f4ae762b1b7ef4e34442d1ad33391 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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232f4ae762b1b7ef4e34442d1ad33391
Registration Details
Taiwan FDA Registration: 232f4ae762b1b7ef4e34442d1ad33391
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Device Details

“Dio” UF(II) Narrow Angled abutment
TW: “帝歐”悠福耐植體系統-角度式支台齒
Risk Class 2
MD

Registration Details

232f4ae762b1b7ef4e34442d1ad33391

Ministry of Health Medical Device Import No. 029629

DHA05602962906

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

Apr 12, 2017

Apr 12, 2027