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"Sleeping Well" Oropharyngeal Airway (Non-Sterile) - Taiwan Registration d9cfaac1cd80d0310c9a30ee94ca1284

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 d9cfaac1cd80d0310c9a30ee94ca1284 and manufactured by SLEEPING WELL, LLC.. The authorized representative in Taiwan is AIREX CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SLEEPING WELL, LLC., 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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d9cfaac1cd80d0310c9a30ee94ca1284
Registration Details
Taiwan FDA Registration: d9cfaac1cd80d0310c9a30ee94ca1284
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Device Details

"Sleeping Well" Oropharyngeal Airway (Non-Sterile)
TW: "ๅˆฉๅ“็ถญ" ๅฃๅ’ฝๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d9cfaac1cd80d0310c9a30ee94ca1284

Ministry of Health Medical Device Import No. 020142

DHA09402014205

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

Mar 06, 2019

Mar 06, 2024

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