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“Trilux” Madidrant CSS Intensive (Non-Sterile) - Taiwan Registration 44e88df45413125f26cbfefd461f564e

Access comprehensive regulatory information for “Trilux” Madidrant CSS Intensive (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 44e88df45413125f26cbfefd461f564e and manufactured by TRILUX MEDICAL GMBH & CO. KG. The authorized representative in Taiwan is T-SUN INTERNATIONAL 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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44e88df45413125f26cbfefd461f564e
Registration Details
Taiwan FDA Registration: 44e88df45413125f26cbfefd461f564e
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Device Details

“Trilux” Madidrant CSS Intensive (Non-Sterile)
TW: “崔勒斯”美帝綸德吊塔系統 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

44e88df45413125f26cbfefd461f564e

Ministry of Health Medical Device Import No. 014776

DHA09401477608

Company Information

Germany

Product Details

I General and plastic surgical devices

I4960 Electric or pneumatic surgical tables, chairs and accessories

Imported from abroad

Dates and Status

Dec 24, 2014

Dec 24, 2019

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延