Taiwan FDA registration 9f11f0e76091a38a5db2bf844d7977a1
"Bantron" fiberglass root column (unsterilized)
TW: “班特朗”玻璃纖維根柱 (未滅菌)
Taiwan·Risk Class 1·PENTRON CLINICAL·Registered Jan 09, 2008 – Jan 09, 2013CancelledRegistration details
- Analysis ID
- 9f11f0e76091a38a5db2bf844d7977a1
- Customs Code
- DHA04400644305
Company information
- Manufacturer
- PENTRON CLINICAL
- Manufacturer Country
- United States
- Authorized Representative
- MONITEX INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3810 Root canal center post
- Import Information
- import
Dates and status
- Registration Date
- Jan 09, 2008
- Expiry Date
- Jan 09, 2013
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bantron" fiberglass root column (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f11f0e76091a38a5db2bf844d7977a1 and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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