"Laili" oropharyngeal airway tube (unsterilized) - Taiwan Registration e994b667a57681d8624cf9dd3b0f8f75
Access comprehensive regulatory information for "Laili" oropharyngeal 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 e994b667a57681d8624cf9dd3b0f8f75 and manufactured by HSINER CO., LTD.. The authorized representative in Taiwan is TAIWAN STANCH 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
Registration Details
e994b667a57681d8624cf9dd3b0f8f75
DHY04300231409
Product Details
Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
D Anesthesiology
D.5110 Oropharyngeal airway tubes
Domestic;; Contract manufacturing
Dates and Status
Dec 09, 2008
Dec 09, 2018
Jun 22, 2022
Cancellation Information
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