"Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·IVOCLAR VIVADENT AG·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 9b4c53ea7f8fa518251f6e5db1f4a68f
- License Form
- Ministry of Health Medical Device Import Registration No. 016380
- Customs Code
- DHA08401638000
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
- 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
Top companies providing products similar to ""Ivoclar Vivadent" Abrasive device and accessories (Non-Sterile)"
Recently registered similar products
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 9b4c53ea7f8fa518251f6e5db1f4a68f 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.