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“Dio” UF(II) Multi abutment - Taiwan Registration 555eb3d636a5d8e79043130d70414f90

Access comprehensive regulatory information for “Dio” UF(II) Multi abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 555eb3d636a5d8e79043130d70414f90 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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555eb3d636a5d8e79043130d70414f90
Registration Details
Taiwan FDA Registration: 555eb3d636a5d8e79043130d70414f90
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Device Details

“Dio” UF(II) Multi abutment
TW: “帝歐”悠福複合型基台
Risk Class 2
MD

Registration Details

555eb3d636a5d8e79043130d70414f90

Ministry of Health Medical Device Import No. 030988

DHA05603098808

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

Mar 22, 2018

Mar 22, 2028