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"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.

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14d744319e1d7e065dbe5fcad9eea4a1
Registration Details
Taiwan FDA Registration: 14d744319e1d7e065dbe5fcad9eea4a1
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Device Details

"Qingxiang Light wave" plastic throat guide tube (sterilized)
TW: ใ€ๆ…ถ็ฅฅๅ…‰ๆณขใ€žๅก‘่† ๅ–‰้ƒจๅฐŽๅผ•็ฎก (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

14d744319e1d7e065dbe5fcad9eea4a1

Company Information

Taiwan, Province of China

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…ง็ฎกๆŽข้‡

ๅœ‹็”ข;; QMS/QSD

Dates and Status

May 29, 2012

May 29, 2017

Dec 02, 2016

Cancellation Information

Logged out

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