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“Dio” Premilled Bar - Taiwan Registration e07b8e0940a857e3a784bc81a1e08ee6

Access comprehensive regulatory information for “Dio” Premilled Bar in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e07b8e0940a857e3a784bc81a1e08ee6 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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e07b8e0940a857e3a784bc81a1e08ee6
Registration Details
Taiwan FDA Registration: e07b8e0940a857e3a784bc81a1e08ee6
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Device Details

“Dio” Premilled Bar
TW: “帝歐”鈦金屬研磨棒
Risk Class 2
MD

Registration Details

e07b8e0940a857e3a784bc81a1e08ee6

Ministry of Health Medical Device Import No. 030246

DHA05603024603

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

Sep 22, 2017

Sep 22, 2027