Taiwan FDA registration e1cf9faf3fe7407728a29021df9a1f12
“Ivoclar Vivadent” Ivotion Bond
TW: “義獲嘉偉瓦登特”義獲先義齒基底材黏著劑
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Oct 31, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- e1cf9faf3fe7407728a29021df9a1f12
- License Form
- Ministry of Health Medical Device Import No. 034995
- Customs Code
- DHA05603499502
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3200 resin dental adhesive
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Ivotion Bond in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1cf9faf3fe7407728a29021df9a1f12 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details. 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.
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