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"Large medium" airway connector (unsterilized) - Taiwan Registration 9873df8ac53680a4f3b00b2df063bb4c

Access comprehensive regulatory information for "Large medium" airway connector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9873df8ac53680a4f3b00b2df063bb4c and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory, 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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9873df8ac53680a4f3b00b2df063bb4c
Registration Details
Taiwan FDA Registration: 9873df8ac53680a4f3b00b2df063bb4c
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Device Details

"Large medium" airway connector (unsterilized)
TW: "ๅคงไธญ" ๆฐฃ้“้€ฃๆŽฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9873df8ac53680a4f3b00b2df063bb4c

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "Airway Connector (D.5810)" of the Administrative Measures for the Classification and Grading of Medical Devices.

D Anesthesiology

D.5810 Airway connectors

Domestic

Dates and Status

Jul 25, 2016

Jul 25, 2026

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