Taiwan FDA registration c8fcf14784501805ecb71bc32dd81eaa
"Camel Man" Imaging Rigid Laryngoscope (Non-sterilized)
TW: "駝人" 影像式硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED·Registered Jan 26, 2024 – Jan 26, 2029ActiveRegistration details
- Analysis ID
- c8fcf14784501805ecb71bc32dd81eaa
- Customs Code
- DHA09402337800
Company information
- Manufacturer
- TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED
- Manufacturer Country
- India
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 26, 2024
- Expiry Date
- Jan 26, 2029
About this record
Access comprehensive regulatory information for "Camel Man" Imaging Rigid Laryngoscope (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c8fcf14784501805ecb71bc32dd81eaa and manufactured by TUOREN MEDICAL DEVICE INDIA PRIVATE LIMITED. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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