Taiwan FDA registration f5d56ae636ae22067d847c7357a0753d
"Driver" Curved Laryngeal Lens (Inexplicated)
TW: "駝人" 可彎曲式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED·Registered Feb 06, 2024 – Feb 06, 2029ActiveRegistration details
- Analysis ID
- f5d56ae636ae22067d847c7357a0753d
- Customs Code
- DHA09402339408
Company information
- Manufacturer
- TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED
- Manufacturer Country
- India
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 06, 2024
- Expiry Date
- Feb 06, 2029
About this record
Access comprehensive regulatory information for "Driver" Curved Laryngeal Lens (Inexplicated) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f5d56ae636ae22067d847c7357a0753d and manufactured by TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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