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“EDENTA” Abrasive device and accessories (Non-Sterile) - Taiwan Registration 1643af39bf9e027e35623936d9b76e23

Access comprehensive regulatory information for “EDENTA” Abrasive device and 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 1643af39bf9e027e35623936d9b76e23 and manufactured by EDENTA AG. The authorized representative in Taiwan is FORSEN ENTERPRISE CO., LTD..

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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1643af39bf9e027e35623936d9b76e23
Registration Details
Taiwan FDA Registration: 1643af39bf9e027e35623936d9b76e23
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Device Details

“EDENTA” Abrasive device and accessories (Non-Sterile)
TW: “安達”研磨裝置及其附件(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

1643af39bf9e027e35623936d9b76e23

Ministry of Health Medical Device Import Registration No. 011788

DHA08401178804

Company Information

Switzerland

Product Details

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

未展延而逾期者