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"Fresh Vision" denture adhesive (unsterilized) - Taiwan Registration 924dafce4ff2cbda7f2264d6eb5ef92b

Access comprehensive regulatory information for "Fresh Vision" denture adhesive (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 924dafce4ff2cbda7f2264d6eb5ef92b and manufactured by BONYF AG. The authorized representative in Taiwan is DAPHA TRADING 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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924dafce4ff2cbda7f2264d6eb5ef92b
Registration Details
Taiwan FDA Registration: 924dafce4ff2cbda7f2264d6eb5ef92b
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Device Details

"Fresh Vision" denture adhesive (unsterilized)
TW: "ๆ–ฐ้ฎฎ่ฆ–"ๅ‡็‰™้ป่‘—ๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

924dafce4ff2cbda7f2264d6eb5ef92b

DHA04401155701

Company Information

Switzerland

Product Details

Limited to the first level of identification range of medical equipment management measures "sodium amino methylcellulose, and/or polyethylene methyl ether calcium sodium maleic acid compound salt denture adhesive (F.3490)".

F Dentistry

F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive

import

Dates and Status

Apr 03, 2012

Apr 03, 2017

Nov 04, 2019

Cancellation Information

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