"Luci" tubing fixture (unsterilized) - Taiwan Registration dfdb3090676ba94c5caed3e3244fdadd
Access comprehensive regulatory information for "Luci" tubing fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfdb3090676ba94c5caed3e3244fdadd and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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.
Device Details
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
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Dates and Status
Sep 05, 2012
Sep 05, 2022
Apr 12, 2024
Cancellation Information
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