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"Aon" Oropharyngeal airway tube (unsterilized) - Taiwan Registration a224d059dbcb2791d08a8cd52c54d080

Access comprehensive regulatory information for "Aon" 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 a224d059dbcb2791d08a8cd52c54d080 and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD, and 1 recent registrations in the same category. 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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a224d059dbcb2791d08a8cd52c54d080
Registration Details
Taiwan FDA Registration: a224d059dbcb2791d08a8cd52c54d080
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Device Details

"Aon" Oropharyngeal airway tube (unsterilized)
TW: "ๆ€กๅฎ‰" ๅฃๅ’ฝๆฐฃ้“็ฎก(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a224d059dbcb2791d08a8cd52c54d080

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

Dates and Status

Mar 02, 2011

Mar 02, 2016

May 28, 2018

Cancellation Information

Logged out

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