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"Bantron" glass fiber reinforced coronary polymer - Taiwan Registration 97d9febef510dbe4803ffacd6c6d5ace

Access comprehensive regulatory information for "Bantron" glass fiber reinforced coronary polymer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97d9febef510dbe4803ffacd6c6d5ace 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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97d9febef510dbe4803ffacd6c6d5ace
Registration Details
Taiwan FDA Registration: 97d9febef510dbe4803ffacd6c6d5ace
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Device Details

"Bantron" glass fiber reinforced coronary polymer
TW: "็ญ็‰นๆœ—" ็Žป็’ƒ็บ–็ถญๅผทๅŒ–ๅ† ๅฟƒ่šๅˆๆ
Risk Class 2

Registration Details

97d9febef510dbe4803ffacd6c6d5ace

DHA00601283004

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dentistry

import

Dates and Status

Oct 27, 2005

Oct 27, 2025