Taiwan FDA registration 6307963a9f59cfd7a19a3a24b79611a7
"Driver Kintek" Curved Laryngeal Lens (Indestructible)
TW: "駝人金泰克" 可彎曲式喉頭鏡(未滅菌)
Taiwan·Risk Class 1·HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.·Registered Aug 05, 2024 – Aug 05, 2029ActiveRegistration details
- Analysis ID
- 6307963a9f59cfd7a19a3a24b79611a7
- Customs Code
- DHA09600496801
Company information
- Manufacturer
- HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Flexible Laryngoscope (D.5530)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5530 Curved laryngeal lenses
- Import Information
- Chinese goods;; QMS/QSD;; input
Dates and status
- Registration Date
- Aug 05, 2024
- Expiry Date
- Aug 05, 2029
About this record
Access comprehensive regulatory information for "Driver Kintek" Curved Laryngeal Lens (Indestructible) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6307963a9f59cfd7a19a3a24b79611a7 and manufactured by HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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