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"Biodenta" Surgical Guide (Non-Sterile) - Taiwan Registration 39429e3aee0957da6e50378e068855ad

Access comprehensive regulatory information for "Biodenta" Surgical Guide (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 39429e3aee0957da6e50378e068855ad and manufactured by BIODENTA SWISS AG. The authorized representative in Taiwan is Dentauspex 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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39429e3aee0957da6e50378e068855ad
Registration Details
Taiwan FDA Registration: 39429e3aee0957da6e50378e068855ad
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Device Details

"Biodenta" Surgical Guide (Non-Sterile)
TW: "็™พไธน็‰น" ๆ‰‹่ก“ๅฐŽๆฟ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

39429e3aee0957da6e50378e068855ad

Ministry of Health Medical Device Import No. 018486

DHA09401848606

Company Information

Switzerland

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

Nov 10, 2017

Nov 10, 2027