“White Dental” Abrasive Device and Accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·KENDA AG·Registered Dec 20, 2019 – Dec 20, 2024Cancelled- Analysis ID
- 88c41cecc5cb1c8d3dfb6812c2c08754
- License Form
- Ministry of Health Medical Device Import No. 021122
- Customs Code
- DHA09402112204
- Manufacturer
- KENDA AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- WHITE DENTAL 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
- Dec 20, 2019
- Expiry Date
- Dec 20, 2024
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for “White Dental” 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 88c41cecc5cb1c8d3dfb6812c2c08754 and manufactured by KENDA AG. The authorized representative in Taiwan is WHITE DENTAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MEDIVANCE INSTRUMENTS LTD, KENDA AG, and 3 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.