Taiwan FDA registration b465586602b6ef988f0279a188c3d0a8
"Camel Kintek" image-based endotracheal probe (unsterilized)
TW: "駝人金泰克" 影像式氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.·Registered May 07, 2019 – May 07, 2024ExpiredRegistration details
- Analysis ID
- b465586602b6ef988f0279a188c3d0a8
- Customs Code
- DHA09600378004
Company information
- Manufacturer
- HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- May 07, 2019
- Expiry Date
- May 07, 2024
About this record
Access comprehensive regulatory information for "Camel Kintek" image-based 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 b465586602b6ef988f0279a188c3d0a8 and manufactured by HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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