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"OMNIMATE" NASOPHARYNGEAL AIRWAY (NON-STERILE) - Taiwan Registration 2f4a01ed4dcbd5173cac4cc473aae4a2

Access comprehensive regulatory information for "OMNIMATE" NASOPHARYNGEAL 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 2f4a01ed4dcbd5173cac4cc473aae4a2 and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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2f4a01ed4dcbd5173cac4cc473aae4a2
Registration Details
Taiwan FDA Registration: 2f4a01ed4dcbd5173cac4cc473aae4a2
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Device Details

"OMNIMATE" NASOPHARYNGEAL AIRWAY (NON-STERILE)
TW: "ๅปฃ้Žฌ" ้ผปๅ’ฝๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2f4a01ed4dcbd5173cac4cc473aae4a2

Ministry of Health Medical Device Manufacturing No. 007788

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".

D Devices for anesthesiology

D5100 Nasopharyngeal airway tube

Produced in Taiwan, China

Dates and Status

May 30, 2019

May 30, 2024