Taiwan FDA registration 1b91725e1e2ce345a8f58b81caa352db
“Ivolcar Vivadent” IvoBase CAD
TW: “義獲嘉偉瓦登特”義獲義齒基底材
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Nov 27, 2019 – Nov 27, 2024ExpiredRegistration details
- Analysis ID
- 1b91725e1e2ce345a8f58b81caa352db
- License Form
- Ministry of Health Medical Device Import No. 033012
- Customs Code
- DHA05603301206
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)
- F3760 Denture re-liner re-reinding or replacement underlay resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 27, 2019
- Expiry Date
- Nov 27, 2024
About this record
Access comprehensive regulatory information for “Ivolcar Vivadent” IvoBase CAD in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1b91725e1e2ce345a8f58b81caa352db and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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