Taiwan FDA registration 97d9febef510dbe4803ffacd6c6d5ace
"Bantron" glass fiber reinforced coronary polymer
TW: "班特朗" 玻璃纖維強化冠心聚合材
Taiwan·Risk Class 2·PENTRON CLINICAL·Registered Oct 27, 2005 – Oct 27, 2025ExpiredRegistration details
- Analysis ID
- 97d9febef510dbe4803ffacd6c6d5ace
- Customs Code
- DHA00601283004
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" glass fiber reinforced coronary polymer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97d9febef510dbe4803ffacd6c6d5ace and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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