"Kenda" Abrasive Device and Accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·KENDA AG·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 440121e33c08f3f0f53e7d503cabb949
- License Form
- Ministry of Health Medical Device Import Registration No. 002603
- Customs Code
- DHA08400260304
- Manufacturer
- KENDA AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- TUNG SHENG INTERNATIONAL INC.
- Intended Use
- It is made of various abrasive materials such as diamond sheets adhering to paper dominated by shellac. It is used to remove excess compound material such as gold and smooth the surface of oral compound objects (such as dental crowns). This device is attached to the handle of the mobile phone for use.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6010 Grinding device and accessories
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for "Kenda" 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 440121e33c08f3f0f53e7d503cabb949 and manufactured by KENDA AG. The authorized representative in Taiwan is TUNG SHENG INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including KENDA AG. DENTAL MANUFACTURING, KENDA AG, and 4 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.