"Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·IVOCLAR VIVADENT AG·Registered Apr 12, 2016 – Apr 12, 2026Cancelled- Analysis ID
- d6a9534ed2760e762175f5fafbc9f474
- License Form
- Ministry of Health Medical Device Import No. 016380
- Customs Code
- DHA09401638006
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6010 Grinding device and accessories
- Import Information
- Imported from abroad
- Registration Date
- Apr 12, 2016
- Expiry Date
- Apr 12, 2026
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Ivoclar Vivadent" 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 d6a9534ed2760e762175f5fafbc9f474 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IVOCLAR VIVADENT AG, 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.