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"DIO" Endosseous dental implant accessories (Non-Sterile) - Taiwan Registration 04834d83836f0d56393968b150cc0120

Access comprehensive regulatory information for "DIO" Endosseous dental implant accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04834d83836f0d56393968b150cc0120 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

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04834d83836f0d56393968b150cc0120
Registration Details
Taiwan FDA Registration: 04834d83836f0d56393968b150cc0120
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Device Details

"DIO" Endosseous dental implant accessories (Non-Sterile)
TW: "ๅธๆญ" ็‰™้ฝ’้ชจๅ…งๆคๅ…ฅ็‰ฉ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

04834d83836f0d56393968b150cc0120

Ministry of Health Medical Device Import No. 013954

DHA09401395401

Company Information

Korea, Republic of

Product Details

Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".

F Dental devices

F3980 Dental Intraosseous Implant Attachment

Imported from abroad

Dates and Status

Mar 11, 2014

Mar 11, 2024