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"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.

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e994b667a57681d8624cf9dd3b0f8f75
Registration Details
Taiwan FDA Registration: e994b667a57681d8624cf9dd3b0f8f75
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Device Details

"Laili" oropharyngeal airway tube (unsterilized)
TW: โ€œ่Š็ฆฎโ€ๅฃๅ’ฝๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e994b667a57681d8624cf9dd3b0f8f75

DHY04300231409

Company Information

Taiwan, Province of China

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

Logged out

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