“Teleflex” Gibeck Humid-Vent HEPA - Taiwan Registration 2348eb2651cf339b0dad33c5e0bb10c6

Access comprehensive regulatory information for “Teleflex” Gibeck Humid-Vent HEPA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2348eb2651cf339b0dad33c5e0bb10c6 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.