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"Zest" Precision attachment (Non-Sterile) - Taiwan Registration 4f9c518822f488270d1449bfb7ac216a

Access comprehensive regulatory information for "Zest" Precision attachment (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 4f9c518822f488270d1449bfb7ac216a and manufactured by ZEST ANCHORS, LLC. 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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4f9c518822f488270d1449bfb7ac216a
Registration Details
Taiwan FDA Registration: 4f9c518822f488270d1449bfb7ac216a
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Device Details

"Zest" Precision attachment (Non-Sterile)
TW: "ๅ‚‘ไป•ๅพท" ็ฒพๅฏ†ๆŽฅ่‘—้ซ” (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4f9c518822f488270d1449bfb7ac216a

Ministry of Health Medical Device Import No. 016021

DHA09401602104

Company Information

United States

Product Details

Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.

F Dental devices

F3165 precision bond

Imported from abroad

Dates and Status

Dec 28, 2015

Dec 28, 2025