Taiwan FDA registration 998daaee92f99ac17cdb91f191f2b56e
“Ivoclar Vivadent” Telio Temporary Restorative Material
TW: “義獲嘉偉瓦登特”特利歐牙科用暫時性修復材料
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Sep 12, 2021 – Sep 12, 2026ActiveRegistration details
- Analysis ID
- 998daaee92f99ac17cdb91f191f2b56e
- License Form
- Ministry of Health Medical Device Import No. 034945
- Customs Code
- DHA05603494500
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)
- F3770 Temporary crown and bridge resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 12, 2021
- Expiry Date
- Sep 12, 2026
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Telio Temporary Restorative Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 998daaee92f99ac17cdb91f191f2b56e and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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