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"Mercury" OROPHARYNGEAL AIRWAY (Non-Sterile) - Taiwan Registration 5491ddcfb4ab606a063f433901c8e18c

Access comprehensive regulatory information for "Mercury" 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 5491ddcfb4ab606a063f433901c8e18c and manufactured by MERCURY MEDICAL. The authorized representative in Taiwan is FRIENDS SCIENTIFIC 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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5491ddcfb4ab606a063f433901c8e18c
Registration Details
Taiwan FDA Registration: 5491ddcfb4ab606a063f433901c8e18c
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Device Details

"Mercury" OROPHARYNGEAL AIRWAY (Non-Sterile)
TW: "่Žซๅฏ็‘ž" ๅฃๅ’ฝๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5491ddcfb4ab606a063f433901c8e18c

Ministry of Health Medical Device Import No. 018664

DHA09401866404

Company Information

United States

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

Dates and Status

Dec 28, 2017

Dec 28, 2022