Taiwan FDA registration f45fd45d3e442b38ffa3a7b4d1f9fb50
"Camel Kintec" one-use laryngoscope blade (sterilized)
TW: “駝人金泰克”一次使用型喉頭鏡葉片 (滅菌)
Taiwan·Risk Class 1·HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.·Registered Jan 07, 2020 – Jan 07, 2030ActiveRegistration details
- Analysis ID
- f45fd45d3e442b38ffa3a7b4d1f9fb50
- Customs Code
- DHA09600406906
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 "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
- Chinese goods;; QMS/QSD;; input
Dates and status
- Registration Date
- Jan 07, 2020
- Expiry Date
- Jan 07, 2030
About this record
Access comprehensive regulatory information for "Camel Kintec" one-use laryngoscope blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f45fd45d3e442b38ffa3a7b4d1f9fb50 and manufactured by HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices