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"Bantron" fiberglass root column (unsterilized) - Taiwan Registration 9f11f0e76091a38a5db2bf844d7977a1

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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9f11f0e76091a38a5db2bf844d7977a1
Registration Details
Taiwan FDA Registration: 9f11f0e76091a38a5db2bf844d7977a1
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Device Details

"Bantron" fiberglass root column (unsterilized)
TW: โ€œ็ญ็‰นๆœ—โ€็Žป็’ƒ็บ–็ถญๆ นๆŸฑ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9f11f0e76091a38a5db2bf844d7977a1

DHA04400644305

Company Information

United States

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 Dentistry

F.3810 Root canal center post

import

Dates and Status

Jan 09, 2008

Jan 09, 2013

Sep 26, 2016

Cancellation Information

Logged out

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