“Ivoclar Vivadent”Resin Impression Tray Material (Non-Sterile)
Taiwan·Risk Class 1·MD·IVOCLAR VIVADENT, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- e6d65cf9071976e1e7ca601dd81d9bf5
- License Form
- Ministry of Health Medical Device Import Registration No. 009449
- Customs Code
- DHA08400944903
- Manufacturer
- IVOCLAR VIVADENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BioLaden Consultant Corp.
- Intended Use
- Limited to the first level identification range of resin impression dental tray (F.3670) of the management method for medical equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3670 resin impression dental tray
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for “Ivoclar Vivadent”Resin Impression Tray Material (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 e6d65cf9071976e1e7ca601dd81d9bf5 and manufactured by IVOCLAR VIVADENT, INC.. 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.