Taiwan FDA registration d44b64e8d98229c43f6925853d730aa0
"Bantron" self-adhesive resin cement
TW: “班特朗”自黏樹脂水泥
Taiwan·Risk Class 2·PENTRON CLINICAL·Registered Jan 11, 2013 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- d44b64e8d98229c43f6925853d730aa0
- Customs Code
- DHA00602443501
Company information
- Manufacturer
- PENTRON CLINICAL
- Manufacturer Country
- United States
- 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.3275 牙科用水泥(士敏汀)
- Import Information
- import
Dates and status
- Registration Date
- Jan 11, 2013
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for "Bantron" self-adhesive resin cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d44b64e8d98229c43f6925853d730aa0 and manufactured by PENTRON CLINICAL. 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