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“Edenta” Abrasive Devices and Accessories(Non-Sterile) - Taiwan Registration b6f3e01607957580a7d5a2e32ce0ebdf

Access comprehensive regulatory information for “Edenta” Abrasive Devices 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 b6f3e01607957580a7d5a2e32ce0ebdf and manufactured by EDENTA AG. The authorized representative in Taiwan is MIDST ENTERPRISE CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EDENTA AG, and 1 recent registrations in the same category. 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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b6f3e01607957580a7d5a2e32ce0ebdf
Registration Details
Taiwan FDA Registration: b6f3e01607957580a7d5a2e32ce0ebdf
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Device Details

“Edenta” Abrasive Devices and Accessories(Non-Sterile)
TW: “爾燈塔”研磨裝置及其附件(未滅菌)
Risk Class 1
MD

Registration Details

b6f3e01607957580a7d5a2e32ce0ebdf

Ministry of Health Medical Device Import Registration No. 020646

DHA08402064601

Company Information

Liechtenstein

Product Details

Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2024

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