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"Bio-Art" Facebow (Non-Sterile) - Taiwan Registration 30923f065c80b13a13b3cba4c9129aa3

Access comprehensive regulatory information for "Bio-Art" Facebow (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 30923f065c80b13a13b3cba4c9129aa3 and manufactured by BIO-ART EQUIPAMENTOS ODONTOLOGICOS LTDA.. The authorized representative in Taiwan is MNM BIOTECHNOLOGY CO., LTD.

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30923f065c80b13a13b3cba4c9129aa3
Registration Details
Taiwan FDA Registration: 30923f065c80b13a13b3cba4c9129aa3
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Device Details

"Bio-Art" Facebow (Non-Sterile)
TW: "็™พๆญ็ˆพ" ้ œ่ˆ‡้ œ้กณ้—œ็ฏ€้—œไฟ‚ไฝ็ฝฎๆธฌ้‡่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

30923f065c80b13a13b3cba4c9129aa3

Ministry of Health Medical Device Import No. 019847

DHA09401984704

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Jaw and Maxillotemporal Joint Relationship Position Meter (F.3220)".

F Dental devices

F3220 Jaw-temporal joint position gauge

Imported from abroad

Dates and Status

Nov 26, 2018

Nov 26, 2028