Taiwan FDA registration c5a4480f50a5b04125fe4d526b74f69e
"Henan Camel Man" endotracheal probe (sterilized)
TW: "河南駝人" 氣管內管探針 (滅菌)
Taiwan·Risk Class 1·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Oct 30, 2019 – Oct 30, 2024ExpiredRegistration details
- Analysis ID
- c5a4480f50a5b04125fe4d526b74f69e
- Customs Code
- DHA09600400404
Company information
- Manufacturer
- HENAN TUOREN 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;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Oct 30, 2019
- Expiry Date
- Oct 30, 2024
About this record
Access comprehensive regulatory information for "Henan Camel Man" endotracheal probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5a4480f50a5b04125fe4d526b74f69e and manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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