“Pentron” FibreKleer 4X (Non-sterile) - Taiwan Registration 8c6efaa29b281da4be74bf780bfcf3d4
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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Device Details
Registration Details
8c6efaa29b281da4be74bf780bfcf3d4
Ministry of Health Medical Device Import No. 013420
DHA09401342003
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
F Dental devices
F3810 tube center column nail
Imported from abroad
Dates and Status
Sep 13, 2013
Sep 13, 2028

