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"Maillefer" Gutta percha (Non-sterile) - Taiwan Registration 1f104075135b4a3ff86906b7493ac73a

Access comprehensive regulatory information for "Maillefer" Gutta percha (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 1f104075135b4a3ff86906b7493ac73a and manufactured by MAILLEFER INSTRUMENTS HOLDING SARL. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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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1f104075135b4a3ff86906b7493ac73a
Registration Details
Taiwan FDA Registration: 1f104075135b4a3ff86906b7493ac73a
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Device Details

"Maillefer" Gutta percha (Non-sterile)
TW: "้บฅๆจ‚ไฝ›" ้ฆฌไพ†่†  (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1f104075135b4a3ff86906b7493ac73a

Ministry of Health Medical Device Import No. 016770

DHA09401677006

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".

F Dental devices

F3850 Male-Glue

Imported from abroad

Dates and Status

Jul 12, 2016

Jul 12, 2026