Taiwan FDA registration 7fec8e8a86816d2240213b5436754c72
“Cavex” Quadrant Universal LC composite Syringes
TW: “佳貝士”夸任特通用型複合材
Taiwan·Risk Class 2·MD·CAVEX HOLLAND B.V.·Registered Feb 03, 2016 – Feb 03, 2026ExpiredRegistration details
- Analysis ID
- 7fec8e8a86816d2240213b5436754c72
- License Form
- Ministry of Health Medical Device Import No. 028188
- Customs Code
- DHA05602818800
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 Universal LC composite Syringes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fec8e8a86816d2240213b5436754c72 and manufactured by CAVEX HOLLAND B.V.. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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