Taiwan FDA registration 1643af39bf9e027e35623936d9b76e23
“EDENTA” Abrasive device and accessories (Non-Sterile)
TW: “安達”研磨裝置及其附件(未滅菌)
Registration details
- Analysis ID
- 1643af39bf9e027e35623936d9b76e23
- License Form
- Ministry of Health Medical Device Import Registration No. 011788
- Customs Code
- DHA08401178804
Company information
- Manufacturer
- EDENTA AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- FORSEN ENTERPRISE CO., LTD.
Product details
- 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, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices