Taiwan FDA registration 25b68b056ca0cc0b0abe7ccd6758dd6e
"Bantlang" fiberglass root column (unsterilized)
TW: “班特朗” 玻璃纖維牙根柱 (未滅菌)
Taiwan·Risk Class 1·PENTRON CLINICAL·Registered Nov 22, 2010 – Nov 22, 2025ExpiredRegistration details
- Analysis ID
- 25b68b056ca0cc0b0abe7ccd6758dd6e
- Customs Code
- DHA04400956100
Company information
- Manufacturer
- PENTRON CLINICAL
- Manufacturer Country
- United States
- Authorized Representative
- MONITEX INDUSTRIAL CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Root Canal Center Pillar (F.3810)" of the Classification and Grading Management Measures for Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3810 Root canal center post
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2010
- Expiry Date
- Nov 22, 2025
About this record
Access comprehensive regulatory information for "Bantlang" 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 25b68b056ca0cc0b0abe7ccd6758dd6e and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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