Taiwan FDA registration 42d3e1eb6c896d32a2393be9d1434ee0
"Ciguang" flexible laryngoscope (unsterilized)
TW: "慈光" 可彎曲式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·Ciguang Technology Co., Ltd·Registered Jul 13, 2012 – Jul 13, 2017CancelledRegistration details
- Analysis ID
- 42d3e1eb6c896d32a2393be9d1434ee0
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 of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5530 Curved laryngeal lenses
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 13, 2012
- Expiry Date
- Jul 13, 2017
- Cancellation Date
- Nov 30, 2018
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Ciguang" flexible laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42d3e1eb6c896d32a2393be9d1434ee0 and manufactured by Ciguang Technology Co., Ltd. The authorized representative in Taiwan is Ciguang Technology Co., Ltd.
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