Taiwan FDA registration 7d36e9e033747b496f06f834b7d0f36d
"Bantron" resin adhesive
TW: "班特朗" 樹脂黏合劑
Taiwan·Risk Class 2·PENTRON CLINICAL·Registered Oct 27, 2005 – Oct 27, 2025ExpiredRegistration details
- Analysis ID
- 7d36e9e033747b496f06f834b7d0f36d
- Customs Code
- DHA00601286905
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
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2005
- Expiry Date
- Oct 27, 2025
About this record
Access comprehensive regulatory information for "Bantron" resin adhesive in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d36e9e033747b496f06f834b7d0f36d 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