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“GaleMed” Oropharyngeal Airway (Non-Sterile) - Taiwan Registration d60b0e2a5e769b3cbe803c80b93f5dfb

Access comprehensive regulatory information for “GaleMed” Oropharyngeal Airway (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d60b0e2a5e769b3cbe803c80b93f5dfb and manufactured by GALEMED (XIAMEN) CO., LTD.. The authorized representative in Taiwan is GALEMED CORPORATION.

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d60b0e2a5e769b3cbe803c80b93f5dfb
Registration Details
Taiwan FDA Registration: d60b0e2a5e769b3cbe803c80b93f5dfb
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Device Details

“GaleMed” Oropharyngeal Airway (Non-Sterile)
TW: “崇仁” 口咽氣道管器材(未滅菌)
Risk Class 1
MD

Registration Details

d60b0e2a5e769b3cbe803c80b93f5dfb

Ministry of Health Medical Device Land Transport No. 004062

DHA09600406205

Company Information

Product Details

Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.

D Devices for anesthesiology

D5110 Oropharyngeal airway tube

Imported from abroad; Made in China

Dates and Status

Dec 27, 2019

Dec 27, 2024