"Kulzer" Abrasive Device and Accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·Kulzer GmbH·Registered Mar 28, 2018 – Mar 28, 2023Cancelled- Analysis ID
- 1f69cbb90231993da85f0702aa597ab3
- License Form
- Ministry of Health Medical Device Import No. 018931
- Customs Code
- DHA09401893101
- Manufacturer
- Kulzer GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BENQ AB DENTCARE CORPORATION
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6010 Grinding device and accessories
- Import Information
- Imported from abroad
- Registration Date
- Mar 28, 2018
- Expiry Date
- Mar 28, 2023
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Kulzer" 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 1f69cbb90231993da85f0702aa597ab3 and manufactured by Kulzer GmbH. The authorized representative in Taiwan is BENQ AB DENTCARE CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Kulzer GmbH, and 1 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.