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"Baredon" denture adhesive (unsterilized) - Taiwan Registration 0aefb57d3cdf512811b0707033e81972

Access comprehensive regulatory information for "Baredon" 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 0aefb57d3cdf512811b0707033e81972 and manufactured by BREDENT GMBH & CO. KG. The authorized representative in Taiwan is Piloter International Trading Corp..

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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0aefb57d3cdf512811b0707033e81972
Registration Details
Taiwan FDA Registration: 0aefb57d3cdf512811b0707033e81972
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Device Details

"Baredon" denture adhesive (unsterilized)
TW: "็™พ็‘ž็™ป"ๅ‡็‰™้ป่‘—ๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0aefb57d3cdf512811b0707033e81972

DHA04401231903

Company Information

Germany

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

Oct 29, 2012

Oct 29, 2017

Dec 05, 2019

Cancellation Information

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