Taiwan FDA registration b6f3e01607957580a7d5a2e32ce0ebdf

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

TW: “爾燈塔”研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·EDENTA AG·Registered Oct 01, 2021 – Oct 31, 2024Expired
Registration details
Analysis ID
b6f3e01607957580a7d5a2e32ce0ebdf
License Form
Ministry of Health Medical Device Import Registration No. 020646
Customs Code
DHA08402064601
Company information
Manufacturer
EDENTA AG
Manufacturer Country
Liechtenstein
Authorized Representative
MIDST ENTERPRISE CO., LTD
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6010 Grinding device and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2024
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About this record

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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