Taiwan FDA registration c74999f18db1676d99e18ebc27b5bf27
"Bantron" polymer resin
TW: "班特朗" 聚合樹脂材
Registration details
- Analysis ID
- c74999f18db1676d99e18ebc27b5bf27
- Customs Code
- DHA00601286803
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" polymer resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c74999f18db1676d99e18ebc27b5bf27 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