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“Sleeping Well” Oropharyngeal Airway (Non-Sterile) - Taiwan Registration f5d951d6b6cab548249d8dad7859a76b

Access comprehensive regulatory information for “Sleeping Well” 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 f5d951d6b6cab548249d8dad7859a76b and manufactured by SLEEPING WELL, LLC.. The authorized representative in Taiwan is AIREX CORP..

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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f5d951d6b6cab548249d8dad7859a76b
Registration Details
Taiwan FDA Registration: f5d951d6b6cab548249d8dad7859a76b
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Device Details

“Sleeping Well” Oropharyngeal Airway (Non-Sterile)
TW: “利品維”口咽氣道管(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

f5d951d6b6cab548249d8dad7859a76b

Ministry of Health Medical Device Import No. 013395

DHA09401339504

Company Information

United States

Product Details

D Devices for anesthesiology

D5110 Oropharyngeal airway tube

Imported from abroad

Dates and Status

Sep 10, 2013

Sep 10, 2018

May 19, 2022

Cancellation Information

Logged out

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