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"bredent" Precision attachment (Non-Sterile) - Taiwan Registration d0e9401d557b6b0369b06a136c028be5

Access comprehensive regulatory information for "bredent" 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 d0e9401d557b6b0369b06a136c028be5 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, 1 companies making similar products including Bredent GmbH & Co. KG, and 1 recent registrations in the same category. 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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d0e9401d557b6b0369b06a136c028be5
Registration Details
Taiwan FDA Registration: d0e9401d557b6b0369b06a136c028be5
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Device Details

"bredent" Precision attachment (Non-Sterile)
TW: "ๅ€ๅพทๆฉ" ็ฒพๅฏ†ๆŽฅ่‘—้ซ” (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

d0e9401d557b6b0369b06a136c028be5

Ministry of Health Medical Device Import No. 014824

DHA09401482406

Company Information

Germany

Product Details

F Dental devices

F3165 precision bond

Imported from abroad

Dates and Status

Jan 08, 2015

Jan 08, 2020

Jun 16, 2022

Cancellation Information

Logged out

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