Taiwan FDA registration a9131a1a37849e4c505e41dd8fd51a4f
“Cavex” Quadrant Flow Composite
TW: “佳貝士”夸任特流動性複合材
Taiwan·Risk Class 2·MD·CAVEX HOLLAND B.V.·Registered Feb 03, 2016 – Feb 03, 2026ExpiredRegistration details
- Analysis ID
- a9131a1a37849e4c505e41dd8fd51a4f
- License Form
- Ministry of Health Medical Device Import No. 028187
- Customs Code
- DHA05602818708
Company information
- Manufacturer
- CAVEX HOLLAND B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- MONITEX INDUSTRIAL CO., LTD.
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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 03, 2016
- Expiry Date
- Feb 03, 2026
About this record
Access comprehensive regulatory information for “Cavex” Quadrant Flow Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9131a1a37849e4c505e41dd8fd51a4f and manufactured by CAVEX HOLLAND B.V.. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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