Teleflex tubing fixture (sterilization) - Taiwan Registration 236d62ed4755c19d938583b6c924dee4
Access comprehensive regulatory information for Teleflex tubing fixture (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 236d62ed4755c19d938583b6c924dee4 and manufactured by Teleflex Medical Sdn.Bhd.. 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)".
D Anesthesiology
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Dates and Status
Jun 24, 2013
Jun 24, 2018
Dec 20, 2019
Cancellation Information
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