Taiwan FDA registration 8c6efaa29b281da4be74bf780bfcf3d4
“Pentron” FibreKleer 4X (Non-sterile)
TW: “班特朗”玻璃纖維根柱 (未滅菌)
Taiwan·Risk Class 1·MD·PENTRON CLINICAL·Registered Sep 13, 2013 – Sep 13, 2028ActiveRegistration details
- Analysis ID
- 8c6efaa29b281da4be74bf780bfcf3d4
- License Form
- Ministry of Health Medical Device Import No. 013420
- Customs Code
- DHA09401342003
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 Dental devices
- Product Type (Level 2)
- F3810 tube center column nail
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 13, 2013
- Expiry Date
- Sep 13, 2028
About this record
Access comprehensive regulatory information for “Pentron” FibreKleer 4X (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8c6efaa29b281da4be74bf780bfcf3d4 and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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