"Teleflex" nasopharyngeal airway tube (unsterilized) - Taiwan Registration 2e5b0ab3f18a6b63ff4c42b2e1ae5ed2
Access comprehensive regulatory information for "Teleflex" nasopharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e5b0ab3f18a6b63ff4c42b2e1ae5ed2 and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is Hehua 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.
Device Details
Product Details
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
D Anesthesiology
D.5100 Nasopharyngeal airway tubes
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Dates and Status
Aug 16, 2012
Aug 16, 2017
Sep 10, 2018
Cancellation Information
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