Taiwan FDA registration 53da44360b09ba9125a356e9348b3f07
"Elchet" image-based cannula probe (unsterilized)
TW: "艾爾契特"影像式插管探條(未滅菌)
Taiwan·Risk Class 1·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Mar 13, 2018 – Mar 13, 2023CancelledRegistration details
- Analysis ID
- 53da44360b09ba9125a356e9348b3f07
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE 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
- Mar 13, 2018
- Expiry Date
- Mar 13, 2023
- Cancellation Date
- Jun 17, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Elchet" image-based cannula 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 53da44360b09ba9125a356e9348b3f07 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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