"Qingxiang Light wave" plastic throat guide tube (sterilized) - Taiwan Registration 14d744319e1d7e065dbe5fcad9eea4a1
Access comprehensive regulatory information for "Qingxiang Light wave" plastic throat guide tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 14d744319e1d7e065dbe5fcad9eea4a1 and manufactured by Qingxiang Guangbo Co., Ltd. The authorized representative in Taiwan is Qingxiang Guangbo 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.
Device Details
Product Details
Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
D Anesthesiology
D.5790 ๆฐฃ็ฎกๅ ง็ฎกๆข้
ๅ็ข;; QMS/QSD
Dates and Status
May 29, 2012
May 29, 2017
Dec 02, 2016
Cancellation Information
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