Taiwan FDA registration 0657522ae917e3204fc8e1865743a740
ADENDA Grinding device and accessories (unsterilized)
TW: 艾登妲 研磨裝置及其附件 (未滅菌)
Taiwan·Risk Class 1·EDENTA AG·Registered Aug 25, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 0657522ae917e3204fc8e1865743a740
- Customs Code
- DHA084a0021607
Company information
- Manufacturer
- EDENTA AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- Lixiang Biomedical Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) of the classification and grading management methods for medical equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6010 Abrasive devices and accessories thereof
Dates and status
- Registration Date
- Aug 25, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for ADENDA Grinding device and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0657522ae917e3204fc8e1865743a740 and manufactured by EDENTA AG. The authorized representative in Taiwan is Lixiang Biomedical 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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