Taiwan FDA registration 019cac51dd5689fe1e36bc2db1b62a0a
"Gabes" Steinby silicon impression material
TW: “佳貝士”史達比矽印模材料
Taiwan·Risk Class 2·CAVEX HOLLAND B.V.·Registered May 11, 2011 – May 11, 2021CancelledRegistration details
- Analysis ID
- 019cac51dd5689fe1e36bc2db1b62a0a
- Customs Code
- DHA00602238900
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 Dentistry
- Product Type (Level 2)
- F.3660 Impression Material
- Import Information
- import
Dates and status
- Registration Date
- May 11, 2011
- Expiry Date
- May 11, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gabes" Steinby silicon impression material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 019cac51dd5689fe1e36bc2db1b62a0a and manufactured by CAVEX HOLLAND B.V.. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices