Taiwan FDA registration cd4cc50374fdc12143b9325786c751d6

"Ciguang" endotracheal probe (unsterilized)

TW: “慈光”氣管內管探針 (未滅菌)

Taiwan·Risk Class 1·Ciguang Technology Co., Ltd·Registered Apr 15, 2010 – Apr 15, 2015Cancelled

Registration details

Analysis ID: cd4cc50374fdc12143b9325786c751d6

Company information

Manufacturer: Ciguang Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Ciguang Technology 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: Domestic

Dates and status

Registration Date: Apr 15, 2010
Expiry Date: Apr 15, 2015
Cancellation Date: Jun 08, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Ciguang" endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd4cc50374fdc12143b9325786c751d6 and manufactured by Ciguang Technology Co., Ltd. The authorized representative in Taiwan is Ciguang Technology Co., Ltd.

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