Taiwan FDA registration 14d744319e1d7e065dbe5fcad9eea4a1

"Qingxiang Light wave" plastic throat guide tube (sterilized)

TW: 〝慶祥光波〞塑膠喉部導引管 (滅菌)

Taiwan·Risk Class 1·Qingxiang Guangbo Co., Ltd·Registered May 29, 2012 – May 29, 2017Cancelled

Registration details

Analysis ID: 14d744319e1d7e065dbe5fcad9eea4a1

Company information

Manufacturer: Qingxiang Guangbo Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Qingxiang Guangbo Co., Ltd

Product details

Intended Use: Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5790 氣管內管探針
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: May 29, 2012
Expiry Date: May 29, 2017
Cancellation Date: Dec 02, 2016

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

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.

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