Taiwan FDA registration ad3c45c819e16fe3ee514520d858dfcf
"Hongkang" endotracheal probe (unsterilized)
TW: “弘康”氣管內管探針(未滅菌)
Taiwan·Risk Class 1·Ciguang Technology Co., Ltd·Registered Feb 14, 2012 – Feb 14, 2017CancelledRegistration details
- Analysis ID
- ad3c45c819e16fe3ee514520d858dfcf
Company information
- Manufacturer
- Ciguang Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MEDLUME SCIENTIFIC 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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Feb 14, 2012
- Expiry Date
- Feb 14, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hongkang" 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 ad3c45c819e16fe3ee514520d858dfcf and manufactured by Ciguang Technology Co., Ltd. The authorized representative in Taiwan is MEDLUME SCIENTIFIC CO., LTD..
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