Taiwan FDA registration 7609a19056f0f3f9a0babd04fb7958b2
“Ivoclar Vivadent” Vivaglass
TW: “義獲嘉偉瓦登特”偉瓦玻璃離子黏合劑
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered May 16, 2018 – May 16, 2023ExpiredRegistration details
- Analysis ID
- 7609a19056f0f3f9a0babd04fb7958b2
- License Form
- Ministry of Health Medical Device Import No. 031083
- Customs Code
- DHA05603108306
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- 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)
- F3275 Dental cement (Sminting)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 16, 2018
- Expiry Date
- May 16, 2023
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Vivaglass in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7609a19056f0f3f9a0babd04fb7958b2 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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