Taiwan FDA registration fe370bbab9fbb985dea1aef9a91760b7
“Ivoclar Vivadent” Callisto CPG
TW: “義獲嘉偉瓦登特”卡利朵牙科用基底合金
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT, INC.·Registered May 31, 2018 – May 31, 2028ActiveRegistration details
- Analysis ID
- fe370bbab9fbb985dea1aef9a91760b7
- License Form
- Ministry of Health Medical Device Import No. 031162
- Customs Code
- DHA05603116202
Company information
- Manufacturer
- IVOCLAR VIVADENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3060 Dentistry uses gold base alloys and precious metal alloys
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 31, 2018
- Expiry Date
- May 31, 2028
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Callisto CPG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe370bbab9fbb985dea1aef9a91760b7 and manufactured by IVOCLAR VIVADENT, INC.. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices