"KENDA" Abrasive device and accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·KENDA AG·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- 4f778489a6e88106fd7c6379f9f73056
- License Form
- Ministry of Health Medical Device Import Registration No. 017886
- Customs Code
- DHA08401788608
- Manufacturer
- KENDA AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- FRANKFURT TECHNOLOGY CO., LTD.
- 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, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 4f778489a6e88106fd7c6379f9f73056 and manufactured by KENDA AG. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including KENDA AG, KENDA AG. DENTAL MANUFACTURING, 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.