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"Dyna" Precision Attachment (Non-Sterile) - Taiwan Registration 72f2caae7ff90f54694b95167c717de4

Access comprehensive regulatory information for "Dyna" 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 72f2caae7ff90f54694b95167c717de4 and manufactured by DYNA DENTAL ENGINEERING B.V.. The authorized representative in Taiwan is DENTAL EASE TECHNOLOGY 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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72f2caae7ff90f54694b95167c717de4
Registration Details
Taiwan FDA Registration: 72f2caae7ff90f54694b95167c717de4
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Device Details

"Dyna" Precision Attachment (Non-Sterile)
TW: "ๆˆด็ด" ็ฒพๅฏ†ๆŽฅ่‘—้ซ” (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

72f2caae7ff90f54694b95167c717de4

Ministry of Health Medical Device Import No. 014345

DHA09401434507

Company Information

Netherlands

Product Details

F Dental devices

F3165 precision bond

Imported from abroad

Dates and Status

Jul 21, 2014

Jul 21, 2019

Jun 07, 2022

Cancellation Information

Logged out

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