Covidiens nasopharyngeal airway tube (sterilized) - Taiwan Registration 13a69c3ac2b262ae960b443d5f119fb3
Access comprehensive regulatory information for Covidiens nasopharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13a69c3ac2b262ae960b443d5f119fb3 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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
Registration Details
13a69c3ac2b262ae960b443d5f119fb3
DHA04401051009
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
Contract manufacturing;; input
Dates and Status
Jun 24, 2011
Jun 24, 2016
Mar 16, 2017
Cancellation Information
Logged out
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